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Semmelweis-Institut

Verlag fr Naturheilkunde
Disclaimer:
The purpose of this book is to provide information about the use of the SANUM
preparations for a wide range of medical problems only. However, illness can
be highly unpredictable, and therefore, one should seek the best possible
medical expertise. No liability is accepted by the author and/or the publishers
for any claims arising from the administration, prescribing strategy or use of
any of the remedies described.

To the Reader:

This Isopathic/Homeopathic Materia Medica of Sanum medicinal products has


been compiled from research conducted by leading homeopathic practitioners
in and outside of Germany. The collected research and uses discussed in the
Materia Medica have been reviewed by a distinguished panel. This valuable
compilation of known medicinal uses of the Isopathic/Homeopathic remedies is
made available to interested practitioners and researchers in many countries.
The production process of the homeopathics covered by this Materia Medica is
strictly based on the German Homeopathic Pharmacopoeia (Homopathisches
Arzneimittelbuch), which essentially has been adopted by many other countries.
However, because not all products, dosage forms or intended uses are available
or approved by the relevant authorities in all national markets, practitioners
are advised to seek local guidance regarding the legal status of the products,
intended uses and type of application in their areas. For example, the oral por-
table SIPS (1 and 2 ml vials) are at this time available only in the United States
of America.
Our thanks to all those who have made publication of this Materia Medica possible
and to the peer reviewers and practitioners who have contributed their time
and effort to disseminate this information.

Dr. Konrad Werthmann

Isopathic/Homeopathic
Materia Medica

Edition 2012
Published by Semmelweis-Institut
Verlag fr Naturheilkunde GmbH
D - 27316 Hoya. Copyright by Semmelwels-Institut
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Edition 2012

Printed in Germany by Druckerei Adam Prettenhofer GmbH & Co. KG


Contents
Preface 9

SANUM Excretion Cure 21

4-Steps-Basic Scheme of SANUM Therapy according to Dr. Werthman 22

Albicansan (fungal preparation) Drops 5X, Amps. 5X, Caps. 4X, 23


Supps. 3X, Ointment 3X

Alkala N (mineral & trace elements) Powder 28

Alkala N (mineral & trace elements) Powder 30


(composition available in USA and Canada)

Arthrokehlan A (bacterial preparation) Drops 6X, Amps. 6X 32

Arthrokehlan U (bacterial preparation) Drops 6X, Amps. 6X 35

Bovisan (bacterial preparation) Drops 6X, Amps. 6X, Caps. 5X, Supps. 5X 38

Calvakehl (fungal preparation) Drops 3X, Tabs. 4X 43

Cerivikehl (herbal preparation) Drops 1X, Amps. 3X 45

Chelate See Pleo Chelate 160

Chrysocor (organ preparation) Amps. 5X 47

Citrokehl (citric acid) Drops 10X/30X/200X, Amps. 10X/30X/200X, 48


Tabs. 10X/30X/200X

Cuprukehl (copper gluconate) Drops 3X, Amps. 4X 51

Episcorit (herbal preparation) Drops 53

Exmykehl (fungal preparation) Drops 5X, Amps. 5X, Supps. 3X 55

Fomepikehl (fungal preparation) Drops 5X, Amps. 5X 58

Formasan (formic acid) Drops 6X/12X/30X/200X, 60


Amps. 6X/12X/30X/200X

Fortakehl (fungal preparation) Drops 5X, Amps. 5X, 6X 62


Tabs. 5X, Caps. 4X, Supps. 3X

Ginkgobakehl (herbal preparation) Drops 1X, 4X, Amps. 4X 68

Grifokehl (fungal preparation) Drops 5X, Amps. 5X 71


Hexacyl (herbal & mineral preparation) Drops 73

Larifikehl (fungal preparation) Drops 5X, Amps. 5X, Caps. 4X, 75

Latensin (bacterial preparation) Drops 6X, Amps. 4X, 6X; 78


Caps. 4X, 6X; Supps. 6X

Leptospermusan (herbal preparation) Drops 1X 84


(USA name: Pleo Spermus)

Leptucin (bacterial preparation) Caps. 6X, Supps. 6X 86


(USA name: Pleo Leptu)

Lipiscor (polyunsaturated fatty acids) Caps. 88

Luffasan (herbal preparation) Tabs. 4X 90

Mapurit L (vitamin and mineral) Caps. 91

Mucedokehl (fungal preparation) Drops 5X, Amps. 5X, Caps. 4X, Supps. 3X 92

Mucokehl (fungal preparation) Drops 5X, Amps. 5X, 6X, 7X; Tabs. 5X, 96
Caps. 4X, Supps. 3X, Ointment 3X, Eye Drops 5X

Mucokehl Atox Drops 6X, Amps. 6X 113

Muscarsan (fungal preparation) Drops 6X, Amps. 4X, Tabs. 6X 115

Nigersan (fungal preparation) Drops 5X, Amps. 5X, 6X, 7X; 119
Tabs. 5X, Caps. 4X, Supps. 3X

Nigersan Atox Drops 6X, Amps. 6X 126

Notakehl (fungal preparation) Drops 5X, Amps. 5X, 6X, 7X; Tabs. 5X, 128
Caps. 4X, Supps. 3X, Ointment 3X

Nota-Quent (fungal preparation) Drops 5X 143

Okoubasan (herbal preparation) Drops 2X, Tabs. 2X 144

Pefrakehl (fungal preparation) Drops 5X, Amps. 6X, Caps. 4X, 146
Supps. 3X, Ointment 3X

Pinikehl (fungal preparation) Drops 5X, Amps. 5X, Caps. 4X, Supps. 4X 156

Pleo Chelate Drops 160

Polysan A (in vitro diagnosticum) Drops 9X 162

Polysan D (in vitro diagnosticum) Drops 9X 164

Polysan Dx (in vitro diagnosticum) Drops 9X 166


Polysan E (in vitro diagnosticum) Drops 9X 168

Polysan G (in vitro diagnosticum) Drops 9X 170

Polysan K (in vitro diagnosticum) Drops 9X 172

Polysan M (in vitro diagnosticum) Drops 9X 174

Polysan Om (in vitro diagnosticum) Drops 9X 176

Polysan R (in vitro diagnosticum) Drops 9X 178

Polysan T (in vitro diagnosticum) Drops 9X 180

Quentakehl (fungal preparation) Drops 5X, Amps. 5X, Caps. 4X, Supps. 3X 182

Rebas (organ preparation) Amps. 5X, 12X; Caps. 4X, 6X; Supps. 4X, 6X 190

Recarcin (bacterial preparation) Drops 6X, Amps. 4X, 6X; Caps. 4X, 6X; Supps. 6X 196

Relivora Complex (herbal preparation) Drops, Amps. 205

Ruberkehl (fungal preparation) Drops 5X, Amps. 5X, Supps. 3X 209

Sankombi (fungal preparation) Drops 5X 214

Sanoryzae (fungal preparation) Drops 6X 216

Sanukehl Acne (bacterial preparation: haptens) Drops 6X, Amps. 5X 218

Sanukehl Brucel (bacterial preparation: haptens) Drops 6X, Amps. 6X 222

Sanukehl Cand (fungal preparation: haptens) Drops 6X, Amps. 5X 226

Sanukehl Coli (bacterial preparation: haptens) Drops 6X, Amps. 7X 230

Sanukehl Klebs (bacterial preparation: haptens) Drops 6X, Amps. 6X 234

Sanukehl Myc (bacterial preparation: haptens) Drops 6X, Amps. 5X 238

Sanukehl Prot (bacterial preparation: haptens) Drops 6X, Amps. 7X 242

Sanukehl Pseu (bacterial preparation: haptens) Drops 6X, Amps. 6X 246

Sanukehl Salm (bacterial preparation: haptens) Drops 6X, Amps. 6X 250

Sanukehl Serra (bacterial preparation: haptens) Drops 6X, Amps. 7X 254

Sanukehl Staph (bacterial preparation: haptens) Drops 6X, Amps. 5X 258

Sanukehl Strep (bacterial preparation: haptens) Drops 6X, Amps. 5X 262

Sanukehl Trich (fungal preparation: haptens) Drops 6X, Amps. 5X 266


Sanumgerman Drops 6X 270
(di-potassium-germanium(IV)-citrate-L(+)lactate)

Sanuvis (lactic acid) Drops 2X/Drops 4X/6X/12X/30X/200X, 272


Amps. 4X/6X/12X/ 30X/200X,
Tabs. 4X/6X/12X/ 30X/200X, Ointment 1X

Selenokehl (sodium selenite) Drops 4X, Amps. 4X 277

Silvaysan (herbal preparation) Caps. 281

Stolonikehl (fungal preparation) Drops 6X 283

Strophanthus 4X Sanum (herbal preparation) Drops 4X, Tabs. 4X 284

Taraxan (herbal preparation) Amps. 3X 288

Thymokehl (organ preparation) Amps. 6X, Caps. 6X, Supps. 6X 290

Usneabasan (herbal preparation) Drops 1X 296

Ustilakehl (fungal preparation) Drops 5X, Amps. 5X, Supps. 5X 298

Utilin (bacterial preparation) Drops 6X, Amps. 4X, 6X; 304


Caps. 4X, 6X; Supps. 6X

Utilin S (bacterial preparation) Drops 6X, Amps. 4X, 6X; 316


Caps. 4X, 6X; Supps. 6X

Verrukehl (fungal preparation) Drops 5X 328

Vitamin B Komplex Sanum N (vitamins) Amps. 329

Vitamin B 12 Sanum (vitamins) Amps. 331

Zinkokehl (zinc gluconate) Drops 3X, Amps. 4X 333

Disease List 336


Preface
Origins of Pleomorphism
From todays perspective, the concepts of pleomorphism and symbiosis are in
separably linked with the name of the great researcher and microbiologist,
Professor Dr. Gnther Enderlein (1872-1968).
The basis for his work was the book published by the French researcher A.
Bechamp, titled Microzymas. It described that, under precisely determined
preconditions, a microorganism can appear in diverse developmental stages
and, especially also in diversified forms, without losing its specific characteris-
tics. The microorganism may vary from the smallest rungs of electron micros-
copic magnitude up to large, multinucleic and highly developed stages, such
as bacteria and fungi.
Moreover, Bechamp was able to prove that all animal and plant cells contain tiny
particles which continue to live after the death of the organism and out of which
microorganisms can develop. In this book, Bechamp laid the foundation for the
concept of pleomorphism. The view that microorganisms can undergo a con
siderable variation in form, without losing their specific functions, stood and
continues to stand diametrically opposed to the prevailing opinion of monomor-
phism, which admits only a single form and function to an organism. Naturally,
that opinion has also resulted in a monomorphistic view of every disease pro-
cess. Thus, in contrast to the opinion of Pasteur, that microorganisms simply
exist without any developmental changes, Enderlein, as a result of intensive re-
search, concluded that the monomorphistic perspective of disease processes
could no longer be maintained and had to be given up in favor of a pleomor-
phic perspective. He proved that every organism houses a primal plant germ in its
erythrocytes, which can indeed become subject of a variation in form due to
exogenic influences.
Pleomorphism and Cyclogeny
The opinion represented by pleomorphic bacteriologists of the fundamental
changeability of forms holds the possibility for microorganisms to abruptly change
from originally nonpathogenic into potentially pathogenic conditions.
Enderlein devoted the bulk of his scientific work which stretched for more than
40 years, to the complex question of pleomorphism, symbiosis and cyclogeny of
microorganisms. He published over 500 scientific articles. His chief work was
titled Bacteria Cyclogeny, Berlin, 1925. In this book he described in detail the
changes and development of the Endobiont in its variable forms and its cycle.
It is currently published by Semmelweis Verlag, Hoya, in the German language; it is
available in English language from Terra Medica Inc., USA, order@terra-medica.com.
This research was initiated by Enderlein in the year 1916, while he was working
on typhoid. In blood using a darkfield microscope he observed mobile, tini-
est living forms, which he later named Spermits, which copulated with higher


organized structures, whereafter the product of the copulation became sud-
denly invisible. Enderlein interpreted this as sexual processes, whereby tiniest,
final products occurred, which are not visible even in the light microscope. He
named the symbiotic, primal plant germ in the erythrocyte Endobiont. This En-
dobiont lives in genuine symbiosis with the host organism, that is, with mutual
benefits. Triggered by external factors, the Endobiont can multiply and develop
a process which can considerably disturb the symbiotic equilibrium. A healthy
organism is capable of restoring the equilibrium. In this process, the more highly
developed pathogenic germs are broken down into nonpathogenic primitive
forms through the copulation described by Enderlein. They leave the body via
the natural organs of elimination.
The Nature of the Primal Germs and Symbiosis
However, the capacity for regenerating symbiosis is usually massively weak
ened through unhealthy lifestyles that are not in harmony with nature! Symbio
sis is abandoned when the symbiont makes itself independent and becomes a
parasite. While doing so, the Endobiont undergoes three basic phases: colloid -
bacterium - fungus. This means, it develops from the nonpathogenic, non-mo-
bile, tiniest albuminoid particle (Protit) - which is to be classified in size with
the viruses (0.01 m) - via the nonpathogenic chondrit stage into the parasitic,
pathogenic stages such as bacterium and fungus. According to Enderlein, they
do not represent unchanging organisms that are independent of each other, but
altogether they form a singular, common cycle, which has its origin in the colloi-
dal, albuminoid substances that are contained inside of each particular cell.
Diseases of the Endobiosis Complex
Assisted by darkfield microscopy and using living blood, Enderlein was able to
deliver clear proof of this vital, microbiological process in both its origin and
cycle. As soon as this vital happening leaves a defined condition of equilibrium,
all signs of parasitism occur, whereby pathogenic microorganisms develop out
of the nonpathogenic symbionts (Protits and Chondrits) - with their enzymatic
and metabolic active properties.
According to Enderlein, all diseases of the Endobiosis complex are based on
the upward development of the Endobiont into higher valenced, parasitic growth
forms with their own metabolism that is harmful for bodily fluids. These disease
processes are difficult to fathom, as they make themselves known in the begin-
ning by functional disorders in most diversified organs, such as, by headaches,
high or low blood pressure, feeling poorly, lassitude, lack of appetite, drab
complexion, coated tongue, wounds in the mouth, pimples, sores, hoarse-
ness, catarrhs, ear noises, diarrhea, reduced capacity for vision and hearing,
depressions, weak concentration or poor memory.
Diseases, however, also indicate healing processes, which attempt to return a
disturbed symbiosis to the original healthy condition. Whether the biological
self-healing forces of the organism will win over the disease, or whether the

10
symbiont is able to develop unchecked into a parasite, depends on the condition
of the milieu in which the disturbance happens. If the inner milieu is damaged
through unhealthy nutrition and lifestyles, through environmental toxins, through
constant infections, or even through psychological depressions, this leads to
a disturbed acid-base equilibrium and as a result our self-healing forces are
incapable of restoring our symbiotic equilibrium. Disease will manifest and dam
age the body. According to Enderlein, the milieu-conditioned cyclogenetic rise
into higher stages of those microorganisms developed from the symbiont always
determine the disease.
Foundations for Isopathic Therapy
Based on this knowledge, Enderlein developed Isopathic Therapy with its speci-
fic biological remedies.
In his Bacteria Cyclogeny, Enderlein describes the development of the two mold
fungi species Aspergillus niger van Tieghem (SA 4-20) and Mucor racemosus
Fresen (SA 4-11), beginning from the primitive phases as tiniest colloidal albu
minoid particles, via the bacterial phase, up to the fungal stage.
Both fungal species, which are likely obtained transplacentally, can occur as
Endobionts in all their developmental stages within mammal bodies. Although
their occurrence may be more or less frequent, they are to be seen as the cause
of numerous ailments. The tubercular and paratubercular diseases, caused by
pathogenic Aspergillus stages, do not occur quite as frequently as the disease
processes more frequently caused by pathogenic Mucor phases arising from
the Mucor symbiosis. The presence of the Endobiont in mammal organisms has
been termed Endobiosis by Enderlein since 1946. By this are meant the apatho
genic, low valanced phases of the Mucor racemosus Fresen (SA 4-11) (Protits,
Symprotits, Chondrits, Fibrin). Fibrin is the highest developmental form of the
Chondrit, before the Endobiont changes from the primitive phase into the bacte
rial phase (analogously to Siphonospora polymorpha v. Brehmer). In these lower
valences, the symbiont supports the metabolism of the host organism, thus
strengthening the defense. The higher the Endobiont rises in its developmental
series, the more it increases in toxicity. The upward development of the Endobi
ont via the Chondrit form and higher is the cause for the endobiontic diseases,
up to the death of the host organism. In the course of this process, the Endobi
ont is most likely partaking in the development of tumors. In the stages of
precancerosis, one finds higher valenced Endobionts in the blood. According
to Devrient, the cancer problem cannot be solved without regard to blood parasitism
and polymorphism of the microorganisms. For Enderlein, cancer is for the
host organism a fermentation and decomposition condition, forced upon it by
a parasitic fungus and its developmental forms.
Because the Endobiont devours protein greedily, its upward development and
the Endobiosis or congestion resulting from it are especially co-created through
improper nutrition. These diseases include vascular changes, pathological coa
gulatory processes, geloses, rheumatism, arthritis, spondylosis, tonsillitis, lym-

11
phogranulomatosis, diabetes, gout, tumors of every type (even those that
are benign and their prestages), anemia, leukemia, cerebral sclerosis and pa-
ralyses.
The restriction of protein intake causes the return to lower phases, which then
leave the body via the organs of excretion.
Latest Researches on the Thesis of Pleomorphism
Besides Enderlein also later researchers confirmed the thesis of pleomorphism.
It could be shown that also eukaryotic cells developed from a symbiotic rela-
tionship between different types of prokaryotes (The Endosymbiontic Theory
according to Lynn Margulis: The other Evolution 1999).
The microbiologist Lida Mattmann demonstrated that the cells of mammals not
only host endobiontic microorganisms but also ones which do not develop a
symbiotic relationship. These are the cell wall deficient bacterial forms, often
called Cell Wall Deficient (CWD) forms (Lida Mattmann: Cell Wall Deficient
Forms Stealth Pathogens, 2001).
The Isopathic Preparations of the Fungal Phase
Another possibility for the breakdown of higher forms into lower stages is the
exogenous supply of the so-called Chondritins in the quoted isopathic thera-
py. According to Enderlein, Chondritins are nonpathogenic, low developmental
stages of diverse fungi, which can be either of a specific nature, as in the Mucor
racemosus Fresen (SA 4-11) and Aspergillus niger von Tieghem (SA 4-20), or of
an unspecific nature such as in Penicillium chrysogenum (SA 4-30) and Penicilli-
um glabrum (SA 4-31).
Chondritins from diverse mold fungi and yeasts are available for application, for
example, in the following preparations (see Table of Contents):
ALBICANSAN, Candida albicans
EXMYKEHL, Candida albicans, Candida parapsilosis, Penicillium roquefortii
FORTAKEHL, Peniclllium roquefortii
MUCEDOKEHL, Mucor mucedo
MUCOKEHL, Mucor racemosus
NIGERSAN, Aspergillus niger
NOTAKEHL, Penicillium chrysogenum
PEFRAKEHL, Candida parapsilosis
QUENTAKEHL, Penicillium glabrum
RUBERKEHL, Aspergillus ruber
SANKOMBI, Mucor racemosus, Aspergillus niger
SANORYZAE, Aspergillus oryzae
STOLONIKEHL, Penicillium brevicompactum (formerly: Penicillium stoloniferum)
These remedies have been developed partly by Enderlein himself and partly on
the basis of his most valuable research. They act in the sense of isopathy; that
means, they are not directed against the disease or its symptoms, but they support

12
the bodys own capabilities for regeneration, whereby genuine healing processes
become possible. Isopathic Therapy normalizes the symbiontic equilibrium bet
ween the Endobiont and its host organism on a basis of species-identical or-
ganisms.
In addition, through the administration of the so-called anti-Chondritins MUCO-
KEHL Atox and NIGERSAN Atox, antibodies for the fungal Chondritins, both
their breakdown and their elimination through the urinary paths, the bronchi, the
skin, and especially the intestine, can be accelerated.
The preparations CALVAKEHL, FOMEPIKEHL, LARIFIKEHL, MUSCARSAN,
PINIKEHL, RUBERKEHL, SANORYZAE, STOLONIKEHL and USTILAKEHL
represent fungal preparations, which have had traditional healing reputations in
folk medicine; these preparations are produced as isopathic substances based
on the knowledge of Prof. Dr. Enderlein.
Treatment of Candidiasis with Isopathic Preparations
ALBICANSAN holds a special position among the isopathic preparations.
The active substance of this preparation contains Chondritins of Candida albi-
cans in diverse homeopathic dilutions. The therapeutic principle of the Candida
preparations is based on the dimorphism of the yeast organism. The microorga-
nism may exist in several growth forms or developmental phases, as yeast and
as fungus. Consequently, it is living proof for the accuracy of Enderleins Theory
of Pleomorphism. In its yeast form, the microorganism exists as a single cell.
Candida yeasts are saprophytic, which become pathogenic only under certain
preconditions. A weakened immune system, or antibiotic treatment, promotes
the pathogenicity of Candida yeast cells enormously. They are the cause for the
far-spreading Candidiasis in the form of a superficial colonization on mucous
membranes.
If the infested host cell dies, the yeast cell comes into contact with dissolving
cell fragments and the cell fluid. This is the signal for the yeast cell to rise within
the cyclogenetic series into a parasitic, mycelia forming fungus, which then grows
invasively into the tissues and, thereby, initiates the widening of tissue lesions.
Researchers have succeeded in cultivating the microorganism as yeast phase
and also as fungal phase, side by side, through appropriate conditions of cultiva
tion. Therefore, the superficial mucous membrane associated forms of Candidia
sis as well as the deeper settled, tissue infiltrating infections, and also massive
intestinal mucosal forms can be treated with ALBICANSAN.
Moreover, the well-proven preparation PEFRAKEHL is available for Candidia
sis therapy. It can also be applied, inter alia, as a cross antigen reaction that
is effective for superficial Candida albicans infections. PEFRAKEHL is a pre
paration from the yeast form of Candida parapsilosis, which is predominantly
isolated from the skin, from nail bed infections, otitis externa and endocarditis
in human beings.

13
EXMYKEHL represents a combination of Candida albicans, Candida para
psilosis and Penicillium roquefortii.
General Information on Isopathic Preparations
The dosage of the preparations always has to be adapted to the responsiveness
and the individual symptoms of the patient during treatment. Every overdose
causes excessive production of decomposition forms which possibly can only be
insufficiently removed by the excretion organs, e.g. through the skin, intestine, uri-
nary paths and bronchi. By repeated administration of the detoxified active fungal
antibodies MUCOKEHL Atox 6X and NIGERSAN Atox 6X (Anti-Chondritins),
the elimination of each form of decomposition is accelerated.
As a rule, it is important to ensure the function of the organs of elimination (stool,
urine, sweat, sputum). Possibly, a detoxification therapy (enemas, baths, teas,
electrolytes) may be required.
Because MUCOKEHL (Mucor racemosus) also effects decongestion of agglu
tinated erythrocytes, leucocytes, thrombocytes, etc., an appropriate massage of
connective tissues and muscles is important during treatment of endobiontic di-
seases.
Every isopathic treatment can be performed with oral, inhalable, or percutaneous-
ly rubbed-in preparations, suppositories, or with injections. These diverse forms
of application can be combined or alternatively administered according to the
situation of the case. The intake, inhalation and rubbing in are milder in effect and
suitable for prophylactic treatments during the injection-free intervals as well as
for follow-up treatments.
The combination of preparations from the endobiontic series is definitely possible
and useful.
Additional Measures
The normalization of the pH value in all diseases of the Endobiosis complex is
of great importance. The preparations ALKALA, SANUVIS, CITROKEHL and
FORMASAN are suitable for this purpose.
In regard to additional biological therapy in general, the therapist naturally re
mains in control of all possibilities during the period of isopathic treatment.
Unfortunately, the fact that focal disturbance fields can limit or cancel the ef-
fectiveness of every holistic treatment is often to be taken into account suffi-
ciently. It should be a precondition to examine the patient and to undertake
sanitizations before the administration of isopathic/homeopathic preparations.
Not only should the usual foci in teeth, tonsils, paranasal sinuses, intestine, etc.
be considered, but also the amalgam fillings that play an important part in the
sense of focal toxicoses through years of releasing mercury. The replacement of
these fillings by neutral materials is desirable.
In all diseases from the Endobiosis complex a nutrition rich in vitamins and vital
substances is of fundamental importance. It is a precondition, not only for the

14
healing process, but also for the effectiveness of every isopathic and immuno-
biological treatment of endobiontic conditions. Nutritional intake requires spe-
cial attention in cases of Endobiosis, including cancer. It should be vegetarian,
rich in raw foods, free from superfine flour, sugar, and all addictive substances.
With a vegetarian diet, attention must be given to include sufficient lactic acid
food for the body.
The Immunobiological Preparations from the Bacterial Phase
Beside the previously described isopathic preparations of the fungal phase, the
immunobiological preparations from the bacterial phase fill an important place
in biological therapy:
ARTHROKEHLAN "A", Formol toxoid of the Propionibacterium acnes DSM 4217
ARTHROKEHLAN "U", Formol toxoid of the Corynebacterium sp. DSM 4223
BOVISAN, Mycobacterium bovis
LATENSIN, Bacillus cereus M.U. 345 a
LEPTUCIN, Propionibacterium avidum
RECARCIN, Bacillus firmus SA. C. 501
SANUKEHL Series, Hapten preparations from typical nosode germs
UTILIN, Bacillus subtilis M.U. 345
UTILIN "S", Mycobacterium phlei F.U. 36
The immunobiological preparations contain diverse fractions of various bacte
rial species, such as cellular extracts and cell wall fragments of polysaccharides
in homeopathic potencies. Only especially suitable strains that were cultivated
under specific conditions (note strain numbers) are used; their effectiveness
has been proven by decades of application. They are able to regulate the course
of a physical immune reaction and to raise the immune systems capacity for
response through their nonspecific stimulation. This is achieved by influencing
diverse sub-populations of lymphoid and phagocytizing cells which take part in
the immune functions. For instance, they indirectly take part in the structuring
of humoral antibodies.
Origin and Development of the Immunobiological Preparations
1. Mycobacteria
Mycobacteria and their fragments effect a strong stimulation of the T-cell system,
inducing cellular defense reactions. This is primarily utilized therapeutically in
tumor diseases, among others (J. Hartmann, Therapeutikon 9, 1990).
Therapy with the preparation UTILIN "S" and BOVISAN goes back historically
to the application of mycobacteria for the treatment of pulmonary tuberculo-
sis by Professor Friedmann in the 1920s. Therefore, an outstanding immuno-
therapy became possible, which worked similarly to the officially sanctioned
BCG inoculation, but without the occasional serious side effects. Professor
Friedmanns preparation was further developed by the former SANUM com-
pany into an identically effective preparation of Mycobacterium phlei from the
special strain F.U. 36 (UTILIN "S"). In recent years, the immunostimulating pro-

15
perties of the cell-wall parts of mycobacteria have been intensively researched,
whereby the equivalence of diverse mycobacterial species has been discovered
(BOVISAN).
2. Bacillus Species
In folk medicine, tea decoctions using hay, excrement from cows, or peat moss
have long been used, without any knowledge of their containing Bacillus subtilis
as active agent. Farmers in many countries utilized hay infusions for curing in
testinal diseases in cattle.
As early as 1887, Metchnikoff described the growth-inhibiting effect of aerobic
soil bacteria, particularly of Bacillus subtilis, against pathogens such as Strep-
tococci, Staphylococci, Salmonella and Mycobacterium tuberculosis.
Works by Ramon and Richou, as well as Jansen and Hirschmann in 1943/44
showed the antitoxic and antibiotic properties of the pathogen, which was gen
erally referred to as Hay bacillus.
However, the first reports about the oral, subcutaneous and intravenous appli
cation of Bacillus subtilis strains came from the former SANUM company in the
years 1938/39 with outstanding therapeutic results. Particularly, its effective-
ness with certain pseudotubercular forms was discovered at that time. The
general stimulating effect on the nonspecific defensive capacity of the human
organism already showed up in these beginnings of Subtilis Therapy. The name
UTILIN has been used under trade mark protection for this new, special re
medy since 1939. In later years, additional Bacillus strains that are closely re-
lated to Bacillus subtilis found their entry into the therapy under the product
names of LATENSIN and RECARCIN.
Preparations with Bacillus species have manifold immunostimulating effects. Clini
cal observations yielded good success in recurring diseases of the urinary tract
and the respiratory organs, in patients with defective immune situations, in
food allergies, as well as other chronic diseases that were brought about by a
reduced immune status (J. Hartmann, Therapeutikon 4, 1990).
3. Corynebacteria and Propionibacteria
The immunobiological preparations ARTHROKEHLAN "A" 6X and ARTHRO-
KEHLAN "U" 6X were developed from the preparations Toxinal and Arthrisinal
which were developed by Dr. von Brehmer from bacterial cultures of Siphonos-
pora polymorpha.
Von Brehmer (1883-1958), a contemporary of Enderlein, originally devoted
himself to virus research involving diseases of plants and animals. During the
examination of an accidentally received human blood sample, he discovered
microorganisms that were partly moving and partly immobile. He called them
Siphonospora polymorpha. He was able to prove that even the smallest fluc-
tuations of the blood pH value within the alkaline area effected the cyclogene-
tic upward development of the Siphonospora toward their pathogenic stages.

16
However, in acidic milieu, these higher stages fall apart again into their nonpa-
thogenic, tiniest developmental stages. These works brought additional proof for
Enderleins publications on pleomorphism and the cyclogeny of the Endobionts
released at the identical time.
From 1935, von Brehmer researched a nonpathogenic Siphonospora vacci-
ne for therapeutic purposes. The first material was obtained from gangrenous
tooth pulps and root granuloma. From these sources, von Brehmer developed
the preparation Toxinal, which was applied for rheumatic arthritic diseases, neu
ralgia and Herpes zoster, and Arthrisinal, a formol toxoid from highly active rod
cultures, with cancer diseases as its chief area of indication.
SANUM-Kehlbeck took over the original cultures of Dr. von Brehmers Research
Institute. After purification and identification, the Propionibacteria and Coryne-
bacteria species were isolated from them. The improved cultures are now for-
ming the basis of the preparations ARTHROKEHLAN "A" 6X and ARTHRO-
KEHLAN "U" 6X.
An additional therapeutic development with Corynebacteria followed in the ap
plication of Corynebacterium parvum for infection prophylaxis. This strain was
later reclassified as Propionibacterium acnes. The activation of the monocyte
macrophage system is a general characteristic of the species Propionibacterium.
Its antibacterial, antiviral, antiparasitic and antitumoral actions are the result.
The latter, in particular, have been intensively examined in the strain Propionibac
terium avidum. Its stimulatory effects on the hematopoietic system qualify it in
immune therapy especially for treatment of myelosuppressive side effects of a
cytostatic or radiation therapy.
4. Sanukehl Preparations - Polysaccarides for Haptenic Therapy
Bacteria and fungi produce toxins which can be the causal trigger for the deve-
lopment of specific diseases. In addition, microbes can develop as microorganis-
ms called Cell Wall Deficient (CWD) forms. Toxins and cell wall deficient forms,
however, cannot be recognized by the bodys immune system due to missing
antigen properties. In the mode of action, SANUKEHL preparations bind to the
pathogenic antigens and their toxins and enable elimination.
The product series of SANUKEHL preparations is based on a special produc-
tion process, in which the polysaccharides of microorganisms are extracted. The
Haptens are made from cell-wall components of originally pathogenic germs.
SANUKEHL Acne, Hapten from Propionibacterium acnes
SANUKEHL Brucel, Hapten from Brucella melitensis
SANUKEHL Cand, Hapten from Candida albicans of Serotypes A and B
SANUKEHL Coli, Hapten from Escherichia coli
SANUKEHL Klebs, Hapten from Klebsiella pneumonia
SANUKEHL Myc, Hapten from Mycobacterium bovis
SANUKEHL Prot, Hapten from Proteus vulgaris

17
SANUKEHL Pseu, Hapten from Pseudomonas aeruginosa
SANUKEHL Salm, Hapten from Salmonella enteriditis
SANUKEHL Serra, Hapten from Serratia marcescens
SANUKEHL Staph, Hapten from Staphylococcus aureus
SANUKEHL Strep, Hapten from Streptococcus pyogenens
SANUKEHL Trich, Hapten from Trichophyton verrucosum
General Comments on Immunobiological Preparations
The purpose of applying bacterial suspensions consists in generating an active
immunity in the living organism by artificial means. From the type and amount
of these antibodies the degree of currently existing immunity can be estimated.
Reactions
When applying the specific and unspecific stimulation therapy local or gene
ralized reactions may occur.
Local Reactions
A local reaction after an injection at the site of disease is desirable to a certain
extent. Such a reaction is noticeable, for example, by increased discharge in
cases of gonorrhea infection, by increased pain in joint affections, by softening
the focus of the disease in trichophytia infections. Such local reactions demons-
trate the effectiveness of the remedies. Undesirable reactions occur occasio-
nally and are always a sign that the applied dosage was too high.
General Reactions
The general reactions may occur as headaches, dizziness, weariness and in-
crease of body temperature. They tend, however, to disappear within 12 hours
without requiring any special treatment. The therapy should only be continued
when all the symptoms have disappeared with a lower dosage.
The Acid-Base Equilibrium
As already mentioned, even fluctuations of the blood pH value in the alkaline
area which is generally preceded by a massive acidification of the tissue
promote the upward development of the symbionts toward parasitic germina-
tion, the cause or support of diseases.
It is undisputed that most of civilization diseases are conditioned by our poor
nutritional habits. The unhealthy lifestyle of human beings through inappropri-
ate nutrition with excessive intake of protein makes one acidified in the actual
sense of the word. The accompanying manifestations of todays civilization di-
seases are always a mesenchymal acidosis with a simultaneously excessively
raised alkaline blood pH value, a pathological acidity quotient, according to
Sander, along with an extremely low defensive factor. These are sure criteria for
a metabolic derailment, with the danger of an acute or chronic disease.
Merely by changing ones nutrition, healthy human beings can expect a ba-
lanced acid-base maintenance by choosing a vegetarian diet. As a supportive

18
measure for the restoration of the acid-base equilibrium, ALKALA "N" is the
perfect treatment, also in cases of excessive acidification of the gastrointestinal
tract with its consequences, such as heartburn and gas.
CITROKEHL supports regulation of cell respiration and acid-base manage-
ment, by counteracting blood alkalosis.
SANUVIS is an additional preparation for regulating the pH value of the blood
and tissue, with L (+) lactic acid as its active constituent. The specialty of SANUVIS
lies in the various potencies which are brought together within the preparation.
The lower potencies serve the raising of cellular respiration, while the higher
potencies serve the elimination of excessive lactic acid concentrations, especially
of the nonphysiological D-(-) lactic acid.
Organ Preparations
THYMOKEHL activates metabolism, stimulates the pre-stages of the T-
lymphocytes to maturation and strengthens the immune system.
CHRYSOCOR, a placenta hydrolysate, contains biogenic stimulators that influ-
ence metabolism by raising the cellular respiration.
REBAS, an organ extract of Peyer's Patches, stimulates the B- and T-Iympho-
cytes, thus strengthening the humoral defenses, and supporting the body in
the maintenance or establishment of an intact immune system.
THYMOKEHL, CHRYSOCOR and REBAS have a positive effect on the
entire metabolism.
Plant Extracts
Plant extracts are for adjunctive therapy for support of the immune system, in
combination with isopathic treatment.
CERIVIKEHL promotes blood flow to the mucous membranes; it has, addi
tionally, a regulatory influence on pathogens in the gastrointestinal area.
GINKGOBAKEHL is based on the active constituent complex of the leaves of
the Ginkgo tree, this is well known from Asian folk medicine.
In RELIVORA Complex, the active substance concentrations of Drosera, Echi-
nacea angustifolia and Juglans are combined for best efficacy. Diseases of the
respiratory tract, frequent general infections and diseases of the skin are a
broad field for application for the RELIVORA Complex.
EPISCORIT is a herbal homeopathic immunostimulant, made from Echinacea
purpurea expressed juice.
LUFFASAN, OKOUBASAN, and USNEABASAN are also herbal homeopa-
thic remedies. LUFFASAN, from the fruits of Luffa operculata, is used in ho-
meopathy mainly for allergic rhinitis and conjunctivitis. USNEABASAN, made
from the lichen Usnea barbata, is predominantly used for illnesses in the head
area (headaches, sunstroke) and together with LUFFASAN for the elimination of

19
heavy metals, while OKOUBASAN, from the tree bark of Okoubaka aubrevillei,
finds its application in detoxifying the gastrointestinal tract, in cases of food in-
tolerance or, prophylactically, for changes in climate and nutrition. Besides, there
are many areas of application for patients who are stressed through pesticides,
insecticides or environmental disorders. These are excellent preparations for de-
toxification of the entire system - especially effective in the early stages of colds
and flus.
With these Three herbal homeopathic remedies the following SANUM Excre-
tion Cure (see page 21) an efficient elimination therapy for heavy metals, toxins
and metabolic waste products can be performed.
STROPHANTHUS 4X Sanum with its active ingredient Strophanthin, as a gen
eral cardiac stimulant, has a rapid effect with a short retention time at the heart
and is indicated in cases of cardiac insufficiency and myocarditis.
HEXACYL is indicated for the elemination of all toxic or infectious damage
with increased degradation of protein such as food intolerance, infections and
intoxications.
TARAXAN is indicated for the stimulation of the liver and kidney function and
thus achieving a cleansing of the connective tissue and blood as well.
Mineral and Trace Element Preparations
An important factor for the maintenance of our health lies in providing the body
with necessary mineral and trace elements. Regulatory processes in the organ
ism, which are the precondition for a regulated metabolic process, cannot take
their course without a stable electrolyte equilibrium of ions, such as sodium, po
tassium, calcium and magnesium.
The trace elements, which according to their name are needed by the body in
only very small amounts, enter catalytically into the metabolic processes. With
out the presence of these Bio-catalysts - including iron, zinc, manganese,
copper, cobalt, iodine and fluorine - many processes that are essential for life
cannot take their course, such as the action of the heart.
These mineral and trace element preparations are offered for a broad applica
tion spectrum: ALKALA N (Na, K), MAPURIT L (Mg), SELENOKEHL (Se),
ZINKOKEHL (Zn), and CUPRUKEHL (Cu), and, of course, they are calibrated
to a perfectly balanced total therapy with all the aforementioned products.

20
SANUM Excretion Cure
1. Monday - Friday: in the morning OKOUBASAN 2X drops in daily alternation
with USNEABASAN drops each with 1x 5-10 (begin with 2-3 drops!)
2. Saturday and Sunday: in the morning LUFFASAN 4X tablets 1x 1-2 daily
(begin with tablet)
3. Additional daily:
SELENOKEHL 4X drops in the morning 1x 10
MAPURIT L capsules at noon 1x 1 and
ZINKOKEHL 3X drops in the evening 1x 10-12
4. Nutrition according to Dr. Werthmann (omitting cows milk, hens eggs and
pork)
5. Duration: numerous weeks or months.

General Dosage Proposal for Children


(They are to be adapted to the clinical picture and the therapy course!)
Fungal Preparations:
For topical or oral administration: 1x daily 1 drop for every year of age (e.g. 5
drops for a 5 year old child); Children over 8 years: dosage as for adults.
SANUKEHL Preparations:
Not suitable for children under 2 years. Children over 2 years: as topical ad-
ministration 1x 1 drop for every year of age (e.g. 5 drops for a 5 year old child)
every 1 or 2 days; Children over 8 years: dosage as for adults.
Bacterial Preparations:
Not suitable for children under 2 years. Children over 2 years: as topical ad-
ministration 1x 1 drop for every year of age (e.g. 5 drops for a 5 year old child)
once or twice weekly; Children over 8 years: dosage as for adults.

21
4-Steps-Basic Scheme of SANUM Therapy according to
Dr. Werthmann
Duration of the treatment: 6 to 8 weeks (depending on the clinical picture and
the course of treatment)
Step 1: Milieu Regulation during the complete therapy duration
Change of nutrition to repair the intestinal mucosas atrophy by omitting
the primary antigens (cows milk and hens eggs)
Deacidification / detoxification:
ALKALA N, SANUVIS, CITROKEHL, FORMASAN;
CERIVIKEHL, OKOUBASAN, USNEABASAN
Substitution:
SELENOKEHL, ZINKOKEHL, MAPURIT L, LIPISCOR, Vitamins
At the same time start with
Step 2: Specific Regulation with fungal preparations
NOTAKEHL (bacterial affections) or
QUENTAKEHL (viral affections) or
FORTAKEHL (intestine affections) or
EXMYKEHL (fungal affections) or
PEFRAKEHL (fungal affections) or
GRIFOKEHL (herpes affections) or
ALBICANSAN (candida affections) or
LARIFIKEHL (respiratory tract and intestine diseases,
primary chronic polyarthritis)
After 10 to 20 days change to
Step 3: Basic Regulation with fungal preparations
MUCOKEHL in the morning and NIGERSAN in the evening or
2x daily SANKOMBI for 5 days,
alternatively with the fungal preparation used in Step 2 for 2 days.
(From Monday to Friday: MUCOKEHL/NIGERSAN or SANKOMBI
and Saturday to Sunday the fungal preparation used in Step 2
according to the scheme 5 - 2 - 5 - 2 for two weeks).
At the same time begin with
Step 4: Immunomodulation with bacterial preparations
LATENSIN, RECARCIN, UTILIN or UTILIN S, BOVISAN;
SANUKEHL preparations

22
Albicansan 3X
Ointment
for rubbing in

Active ingredient: Candida albicans e volumine cellulae (lyophil., steril.) 3X

Composition: 1 g ointment contains: Medically active substance: 0.1 g Candida


albicans e volumine cellulae (lyophil., steril.) 3X dil. Other
constituents: 0.38 g lanolin alcohol ointment, 0.10 g coconut oil fract.,
0.03 g glyceryl monostearate 40-55%, 0.23 g propylene glycol, 0.02
g magnesium sulphate x 7 H2O, 0.01 g lactic acid, 0.13 g water for
injection.

According to experience, Mycoses and secondary mycotic, infectious skin disorders, balanitis,
to be administered in vulvitis, pruritis genitalis.
cases of:

Characteristics: Albicansan is gained from mold fungus Candida albicans and is


administered in cases of mycoses of the gastrointestinal tract, the skin
and the mucosa due to Candida albicans infestation.

Application: Unless otherwise prescribed: Apply thinly on the affected area 1 to 3 x


daily.

Side effects: Because of specific organic components of Albicansan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Candida albicans).

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: Candida albicans as an active ingredient is also contained in Exmykehl.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X, 30 g tube
of ointment 3X.

23
Albicansan 3X
Suppositories
for rectal application

Active ingredient: Candida albicans e volumine cellulae (lyophil., steril.) 3X

Composition: 1 suppository contains: Medically active substance: 0.2 g Candida


albicans e volumine cellulae (lyophil., steril.) 3X trit. Other
constituents: hard fat, lactose.

According to experience, Mycoses and secondary mycotic, infectious skin disorders, diseases
to be administered in of the mouth, like stomatitis, gingivitis, perlche, aphthae, mycoses
cases of: of the urogenital tract, such as vaginitis, urethritis, possibly for adnexitis,
mycoses of the gastrointestinal tract.

Characteristics: Albicansan is gained from mold fungus Candida albicans and is


administered in cases of mycoses of the gastrointestinal tract, the skin
and the mucosa due to Candida albicans infestation.

Application: Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally.


Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Albicansan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Candida albicans).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Albicansan.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.


Candida albicans as an active ingredient is also contained in Exmykehl.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X, 30 g tube
of ointment 3X.

24
Albicansan 4X
Capsules
for oral intake

Active ingredient: Candida albicans e volumine cellulae (lyophil., steril.) 4X

Composition: 1 capsule contains: Medically active substance: 330 mg Candida


albicans e volumine cellulae (lyophil., steril.) 4X trit. Other
constituents: lactose, hypromellosis (capsule shell).

According to experience, Mycoses and secondary mycotic, infectious skin disorders, diseases
to be administered in of the mouth, like stomatitis, gingivitis, perlche, aphthae, mycoses of
cases of: the urogenital tract, such as vaginitis, urethritis, possibly for adnexitis,
mycoses of the gastrointestinal tract.

Characteristics: Albicansan is gained from mold fungus Candida albicans and is


administered in cases of mycoses of the gastrointestinal tract, the skin
and the mucosa due to Candida albicans infestation.

Application: Unless otherwise prescribed: 1-3 x daily 1 capsule.


Children between the age of 6 and 12 years should not receive more
than 2/3 of the dosage for adults.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Albicansan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Candida albicans).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Albicansan.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.


Candida albicans as an active ingredient is also contained in
Exmykehl.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X, 30 g tube
of ointment 3X.

25
Albicansan 5X
Ampules
Liquid dilution for injection

Active ingredient: Candida albicans e volumine cellulae (lyophil., steril.) 5X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Candida


albicans e volumine cellulae (lyophil., steril.) 5X aquous dil.
Other constituents: isotonic sodium chloride solution.

According to experience, Mycoses and secondary mycotic, infectious skin disorders, diseases of
to be administered in the mouth, like stomatitis, gingivitis, perlche, aphthae, mycoses of
cases of: the urogenital tract, such as vaginitis, urethritis, possibly for adnexitis,
mycoses of the gastrointestinal tract.

Characteristics: Albicansan is gained from mold fungus Candida albicans and is


administered in cases of mycoses of the gastrointestinal tract, the skin
and the mucosa due to Candida albicans infestation.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3
x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Albicansan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Candida albicans).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Albicansan.


with other remedies: An interval of 4 weeks before and After treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: Candida albicans as an active ingredient is also contained in


Exmykehl.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X, 30 g tube
of ointment 3X.

26
Albicansan 5X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Candida albicans e volumine cellulae (lyophil., steril.) 5X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Candida albicans e volumine cellulae (lyophil., steril.) 5X dil.
Other constituents: purified water.

According to experience, Mycoses and secondary mycotic, infectious skin disorders, diseases of
to be administered in the mouth, like stomatitis, gingivitis, perlche, aphthae, mycoses of
cases of: the urogenital tract, such as vaginitis, urethritis, possibly for adnexitis,
mycoses of the gastrointestinal tract.

Characteristics: Albicansan is gained from mold fungus Candida albicans and is


administered in cases of mycoses of the gastrointestinal tract, the skin
and the mucosa due to Candida albicans infestation.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops before
a meal. For rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Children between the age of 6 and 12 years should not receive more
than 2/3 of the dosage for adults.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Albicansan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Candida albicans).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Albicansan.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: After opening, contents must be used within two months. Candida
albicans as an active ingredient is also contained in Exmykehl.

Duration of treatment: Dependent on the advice of the physician or health careprofessional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X, 30 g tube
of ointment 3X.

27
Alkala
N
Powder

Active ingredients: sodium hydrogen carbonate, potassium hydrogen carbonate,


sodium citrate

Composition: 150 g powder contain: 2.67 g sodium hydrogen carbonate x


H2O, 13.40 g potassium hydrogen carbonate, 133.93 g sodium
citrate.

Indications: Alkalisation, acidosis of the stomach and the duodenum, heartburn,


gastritis and ulcus ventriculi, liver and gallbladder troubles, repletion
and flatulence, rheumatic diseases, chronic skin diseases and diseases
of the respiratory and urogenital tract.

Characteristics: Alkala N is a base mixture, excellently suited for correction of the


organisms acid-base balance. Ideally this relation is balanced in the
human being. Dislocations of the acid-base balance towards the acid
range are nowadays more frequent due to our lifestyla and environmental
conditions. The first typical symptoms for hyperacidity in the stomach
and intestinal area are heartburn, acid regurgitation, flatulence, etc. Sub
sequently, hyperacidity is a typical accompanying symptom of chronic
metabolic disorders which can result in degeneration of the cells.

Application: Use enclosed spoon. Take one spoonful in the morning with a glass of
water. If needed, take a second spoonful in the evening. Do not take
more than two spoonfuls in a 24-hour period.

Side effects: Frequently repletion and eructation. Long term use promotes the
development of calcium and magnesium phosphate kidney stones.

Contraindications: Anacidity of the stomach.

Adverse reactions: None known.

Interactions The absorption and excretion of weak acids and bases can be influenced
with other remedies: through the increasing pH value in the stomach and urine. Functional
interactions are possible with gluco- and mineralocorticoids, androgens
and diuretics which increase the excretion of potassium.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Due to the risk of stomach rupture, Alkala N should not be taken in
cases of acid burn.

Advice: In case of disturbed excretion (anuria, renal insufficiency) and exsic


cation (exsiccosis through water deficiency) as well as in alcalosis
Alkala N should only be taken under medical advice.

28
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: Container with 150 g powder.

29
Alkala
N
Powder
This composition of Alkala N ist only available on the US and Canadian
market.

Active ingredients: sodium hydrogen carbonate, potassium hydrogen carbonate,


sodium citrate

Composition: 150 g powder contain: 2.67 g sodium hydrogen carbonate x H2O,


13.40 g potassium hydrogen carbonate, 133.93 g sodium citrate.
Other constituents: 2,34 g calcium lactate, 2,34 g, sea salt 2,34 g, 11,72
g sodium sulfate.

Indications: Alkalisation, acidosis of the stomach and the duodenum, heartburn,


gastritis and ulcus ventriculi, liver and gallbladder troubles, repletion
and flatulence, rheumatic diseases, chronic skin diseases and diseases
of the respiratory and urogenital tract.

Characteristics: Alkala N is a base mixture, excellently suited for correction of the


organisms acid-base balance. Ideally this relation is balanced in the
human being. Dislocations of the acid-base balance towards the acid
range are nowadays more frequent due to our lifestyle and environmental
conditions. The first typical symptoms for hyperacidity in the stomach
and intestinal area are heartburn, acid regurgitation, flatulence, etc.
Subsequently hyperacidity is a typical accompanying symptom of
chronic metabolic disorders which can result in degeneration of the
cells.

Application: Use enclosed spoon. Take one spoonful in the morning with a glass of
water. If needed, take a second spoonful in the evening. Do not take
more than two spoonfuls in a 24-hour period.

Side effects: Frequently repletion and eructation. Long term use promotes the
development of calcium and magnesium phosphate kidney stones.

Contraindications: Anacidity of the stomach.

Adverse reactions: None known.

Interactions The absorption and excretion of weak acids and bases can be influenced
with other remedies: through the increasing pH value in the stomach and urine. Functional
interactions are possible with gluco- and mineralocorticoids, androgens
and diuretics which increases the excretion of potassium.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.
Due to the risk of stomach rupture, Alkala N should not be taken in
cases of acid burn.

30
Advice: In case of disturbed excretion (anuria, renal insufficiency) and exsic
cation (exsiccosis through water deficiency) as well as in alcalosis
Alkala N should only be taken under medical advice.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: Container with 150 g powder.

31
Arthrokehlan A 6X
Ampules
Liquid dilution for injection

Active ingredient: Propionibacterium acnes culturae filtratum (lyophil., steril.)


6X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Propioni


bacterium acnes culturae filtratum (lyophil., steril.) 6X aquous
dil. Other constituents: isotonic sodium chloride solution.

According to experience, Arthritic, arthrotic, as well as degenerative diseases of the spinal column,
to be administered in myalgia.
cases of:

Characteristics: Arthrokehlan A is produced by inoculation of Siphonospora


polymorpha, which is isolated from the bacterial flora of human dental
granuloma, with Propionibacterium acnes. In accordance with
Dr.von Brehmers method, a formol toxoid (a detoxified culture filtrate)
is produced from these cultures. It effects a sustained rise in defensive
capacity.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected intra


muscularly or subcutaneously, 1-2 x weekly.

Side effects: Because of specific organic components of Arthrokehlan A,


theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.

Contraindications: Fever, conditions of weakness.


Do not administer in cases of known hypersensitivity to Propioni
bacterium acnes.

Adverse reactions: None known. Generally well tolerated. Occasionally local reactions
like rubefaction, swelling or painfulness may be observed, normally
vanishing without treatment. These effects are not to be seen as
adverse reactions, but rather as an expression of effectiveness. In the
first 2 or 3 days after the injection sometimes conditions of weakness,
fortified expectoration, slight painfulness of the region or subfebrile
temperatures may show. Strong general reactions are always a sign of
overdose or of incorrect injection technique.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

32
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.

33
Arthrokehlan A 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Propionibacterium acnes culturae filtratum (lyophil., steril.)


6X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Propionibacterium acnes culturae filtratum (lyophil., steril.)
6X dil. Other constituents: purified water.

According to experience, Arthritic, arthrotic, as well as degenerative diseases of the spinal column,
to be administered in myalgia.
cases of:

Characteristics: Arthrokehlan A is produced by inoculation of Siphonospora


polymorpha, which is isolated from the bacterial flora of human dental
granuloma, with Propionibacterium acnes. In accordance with
Dr.von Brehmers method, a formol toxoid (a detoxified culture filtrate)
is produced from these cultures. It effects a sustained rise in defensive
capacity.

Application: Unless otherwise prescribed: For oral intake: 1-3 x weekly 2-5 drops
before a meal. For rubbing in: 1-3 x weekly 2-5 drops into the bend of
the elbow.

Side effects: Because of specific organic components of Arthrokehlan A,


theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.

Contraindications: Fever, conditions of weakness.


Do not administer in cases of known hypersensitivity to Propioni
bacterium acnes.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.

34
Arthrokehlan U 6X
Ampules
Liquid dilution for injection

Active ingredient: Corynebacterium stationis culturae filtratum (lyophil., steril.)


6X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Coryne


bacterium stationis culturae filtratum (lyophil., steril.) 6X
aquous dil. Other constituents: isotonic sodium chloride solution.

According to experience, Stimulation of endogenic defense capacities, adjuvant in anti-carcino-


to be administered in genic therapy.
cases of:

Characteristics: Arthrokehlan U is produced by inoculation of Siphonospora


polymorpha, which is isolated from the bacterial flora of human dental
granuloma, with Corynebacterium stationis. In accordance with
Dr.von Brehmers method, a formol toxoid (a detoxified culture filtrate)
is produced from these cultures. It effects a sustained rise in defensive
capacity.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected


intramuscularly or subcutaneously, 1-2 x weekly.

Side effects: Because of specific organic components of Arthrokehlan U,


theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.

Contraindications: Fever, conditions of weakness.


Do not administer in cases of known hypersensitivity to Coryne
bacterium stationis.

Adverse reactions: None known. Generally well tolerated. Occasionally local reactions
like rubefaction, swelling or painfulness may be observed, normally
vanishing without treatment. These effects are not to be seen as
adverse reactions, but rather as an expression of effectiveness. In the
first 2 or 3 days after the injection sometimes conditions of weakness,
fortified expectoration, slight painfulness of the region or subfebrile
temperatures may show. Strong general reactions are always a sign of
overdose or of incorrect injection technique.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

35
Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.

36
Arthrokehlan U6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Corynebacterium stationis culturae filtratum (lyophil., steril.)


6X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Coryne


bacterium stationis culturae filtratum (lyophil., steril.) 6X dil.
Other constituents: purified water.

According to experience, Stimulation of endogenic defense capacities, adjuvant in anti-carcino-


to be administered in genic therapy.
cases of:

Characteristics: Arthrokehlan U is produced by inoculation of Siphonospora


polymorpha, which is isolated from the bacterial flora of human dental
granuloma, with Corynebacterium stationis. In accordance with
Dr.von Brehmers method, a formol toxoid (a detoxified culture filtrate)
is produced from these cultures. It effects a sustained rise in defensive
capacity.

Application: Unless otherwise prescribed: For oral intake: 1-3 x weekly 2-5 drops
before a meal. For rubbing in: 1-3 x weekly 2-5 into the bend of the
elbow.

Side effects: Because of specific organic components of Arthrokehlan U,


theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.

Contraindications: Fever, conditions of weakness.


Do not administer in cases of known hypersensitivity to Coryne
bacterium stationis.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.

37
Bovisan 5X
Capsules
for oral intake

Active ingredient: Mycobacterium bovis (BCG) e volumine ex muris cellulae


(lyophil., steril.) 5X

Composition: 1 capsule contains: Medically active substance: 330 mg Myco


bacterium bovis (BCG) e volumine ex muris cellulae (lyophil.,
steril.) 5X trit. Other constituents: lactose, hypromellosis (capsule shell).

According to experience, Chronic inflammation, rheumatic disorders, diseases connected to tuber-


to be administered in culinic constitution; immune modulation.
cases of:

Characteristics: This product is obtained by a special preparation and culture technique


of a stock solution of Mycobacterium bovis which ensures both non-
pathogenic and immunomodulating properties.

Application: Unless otherwise prescribed: 1-2 x weekly 1 capsule.


Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Bovisan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


Do not administer in cases of known hypersensitivity to Mycobacterium
bovis.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Bovisan . An


with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X, 5 capsules 5X, 10 suppositories 5X.

38
Bovisan 5X
Suppositories
for rectal application

Active ingredient: Mycobacterium bovis (BCG) e volumine ex muris cellulae


(lyophil., steril.) 5X

Composition: 1 suppository contains: Medically active substance: 0.2 g Myco


bacterium bovis (BCG) e volumine ex muris cellulae (lyophil.,
steril.) 5X trit. Other constituents: hard fat, lactose.

According to experience, Chronic inflammation, rheumatic disorders, diseases connected to tuber-


to be administered in culinic constitution; immune modulation.
cases of:

Characteristics: This product is obtained by a special preparation and culture technique


of a stock solution of Mycobacterium bovis which ensures both non-
pathogenic and immunomodulating properties.

Application: Unless otherwise prescribed: 1-3 x weekly insert 1 suppository rectally.


Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Bovisan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


Do not administer in cases of known hypersensitivity to Mycobacterium
bovis.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Bovisan.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X, 5 capsules 5X, 10 suppositories 5X.

39
Bovisan 6X
Ampules
Liquid dilution for injection

Active ingredient: Mycobacterium bovis (BCG) e volumine cellulae (lyophil., steril.)


6X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Myco


bacterium bovis (BCG) e volumine cellulae (lyophil., steril.)
6X aquous dil. Other constituents: isotonic sodium chloride solution.

According to experience, Chronic inflammation, rheumatic disorders, diseases connected to tuber-


to be administered in culinic constitution; immune modulation.
cases of:

Characteristics: This product is obtained by a special preparation and culture technique


of a stock solution of Mycobacterium bovis which ensures both non-
pathogenic and immunomodulating properties.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly or subcutaneously 1-2 x weekly.

Side effects: Because of specific organic components of Bovisan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


Do not administer in cases of known hypersensitivity to Mycobacterium
bovis.

Adverse reactions: None known. Generally well tolerated. Occasionally local reactions
like rubefaction, swelling or painfulness may be observed, normally
vanishing without treatment. These effects are not to be seen as
adverse reactions, but rather as an expression of effectiveness. In the
first 2 or 3 days after the injection, sometimes conditions of weakness,
fortified expectoration, slight painfulness of the region or subfebrile
temperatures may occur. Strong general reactions are always a sign of
overdosage or of incorrect injection technique. In this case the treatment
can be continued orally with Bovisan drops or capsules.

Interactions Immunosuppressive drugs can influence the effectivity of Bovisan.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: None.

40
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X, 5 capsules 5X, 10 suppositories 5X.

41
Bovisan 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Mycobacterium bovis (BCG) e volumine cellulae (lyophil., steril.)


6X

Composition: 5 ml liquid dilution contain: Medically active substance: 5 ml Myco


bacterium bovis (BCG) e volumine cellulae (lyophil., steril.)
6X dil. Other constituents: purified water.

According to experience, Chronic inflammation, rheumatic disorders, diseases connected to


to be administered in tuberculinic constitution; immune modulation.
cases of:

Characteristics: This product is obtained by a special preparation and culture technique


of a stock solution of Mycobacterium bovis which ensures both non-
pathogenic and immunomodulating properties.

Application: Unless otherwise prescribed: For oral intake: 1-3 x weekly 2-5 drops.
For rubbing in: 1-3 x weekly 2-5 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Bovisan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


Do not administer in cases of known hypersensitivity to Mycobacterium
bovis.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Bovisan.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X, 5 capsules 5X, 10 suppositories 5X.

42
Calvakehl 3X
Drops
Liquid dilution for oral intake

Active ingredient: Calvatia gigantea e sporibus 3X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Calvatia gigantea e sporibus 3X dil. Other constituents: purified
water, ethanol 62 % (m/m).

According to experience, Bleeding tendency, such as nose bleeding or uterus bleeding; weakness
to be administered in of the heart and circulatory system with blood congestion; lack of oxygen in
cases of: blood; skin rashes; indigestion and diarrhea.

Characteristics: Calvakehl is produced from the Giant bovista fungus. In the 16th
century, the application was already well known in folk medicine for its
hemostyptic and wound healing properties.

Application: Unless otherwise prescribed:


For oral intake: 1-3 x daily 5-10 drops.

Side effects: Because of specific organic components of Calvakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Calvatia


gigantea.
This product contains 70 % (v/v) alcohol (ethanol). Following the
dosage recommendations, 10 drops lead to an alcohol intake of 0.11
g. This may present a health risk in cases of liver diseases, alcoholism,
epilepsy, brain damage, pregnancy, and in children. The action of other
drugs may be reduced or intensified.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains 70 % (v/v) alcohol (ethanol).

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml and 30 ml dropper
bottle 3X, 80 tablets 4X.

43
Calvakehl 4X
Tablets
for oral intake

Active ingredient: Calvatia gigantea e sporibus 4X

Composition: 1 tablet contains: Medically active substance: 250 mg Calvatia


gigantea e sporibus 4X trit. Other constituents: lactose, potato
starch, magnesium stearate.

According to experience, Bleeding tendency, such as nose bleeding or uterus bleeding; weakness
to be administered in of the heart and circulatory system with blood congestion; lack of oxygen
cases of: in blood; skin rashes; indigestion and diarrhea.

Characteristics: Calvakehl is produced from the Giant bovista fungus. In the 16th
century, the application was already well known in folk medicine for its
hemostyptic and wound healing properties.

Application: Unless otherwise prescribed:


For oral intake: 1-3 x daily 1 tablet.

Side effects: Because of specific organic components of Calvakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Calvatia


gigantea.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml and 30 ml dropper
bottle 3X, 80 tablets 4X.

44
Cerivikehl 1X
Drops
Liquid dilution for oral intake

Active ingredient: Cetraria islandica mother tincture

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Cetraria


islandica 1X dil. Other constituents: purified water, ethanol 62% (m/m).

According to experience, Diseases of the respiratory system, sinusitis, laryngitis, bronchitis, dry
to be administered in cough; lack of appetite.
cases of:

Characteristics: Cerivikehl, a plant remedy made of the lichen Icelandic Moss,


is generally used for the promotion of the circulation of the mucous
membranes. A certain constituent of the lichen acids manifests a mild
antibiotic action toward pathogens in oral, pharyngeal and intestinal
infections; it neither leads to the formation of antibiotic-resistant
bacteria nor to allergic reactions.

Application: Unless otherwise prescribed:


in case of acute conditions: up to 6 x daily 5 drops.
in case of chronic forms: 1-3 x daily 5 drops.

Side effects: Because of specific organic components of Cerivikehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: This product contains 70 % (v/v) alcohol (ethanol). Following the


dosage recommendations, 10 drops lead to an alcohol intake of 0.11
g. This may present a health risk in cases of liver diseases, alcoholism,
epilepsy, brain damage, pregnancy, and in children. The action of other
drugs may be reduced or intensified.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains 70 % (v/v) alcohol (ethanol).

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 30 ml dropper bottle 1X, 2 ml
ampule 10 and 50 3X.

45
Cerivikehl 3X
Ampules
Liquid dilution for injection

Active ingredient: Cetraria islandica 3X

Composition: 1 ampule of 2 ml contains: Medically active substance: 2 ml


Cetraria islandica 3X aquous dil. Other constituents: isotonic
sodium chloride solution.

According to experience, Diseases of the respiratory system, sinusitis, laryngitis, bronchitis, dry
to be administered in cough; lack of appetite.
cases of:

Characteristics: Cerivikehl, a plant remedy made of the lichen Icelandic Moss,


is generally used for the promotion of the circulation of the mucous
membranes. A certain constituent of the lichen acids manifests a mild
antibiotic action toward pathogens in oral, pharyngeal and intestinal
infections; it neither leads to the formation of antibiotic-resistant
bacteria nor to allergic reactions.

Application: Unless otherwise prescribed:


1 ampule of 2 ml to be injected either intramuscularly, subcutaneously,
intracutaneously or intravenously, 1 x daily.

Side effects: Because of specific organic components of Cerivikehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 30 ml dropper bottle 1X, 2 ml
ampule 10 and 50 3X.

46
Chrysocor 5X
Ampules
Liquid dilution for injection

Active ingredient: Placenta hydrolysate (lyophil., steril.) 5X

Composition: 1 ampule of 2 ml contains: Medically active substance: 2 ml Placenta


hydrolysate (lyophil., steril.) 5X aquous dil. Other constituents:
isotonic sodium chloride solution.

According to experience, Functional disorders of the male gonads, conditioned by disease or old
to be administered in age, climacterium virile, sexual adynamia, sexual asthenia, hypogenitalism;
cases of: adjuvant for cellular regeneration therapy.

Characteristics: Chrysocor contains a placenta hydrolysate which is administered


for stimulation of metabolism. According to Filatow, placenta extract
contains biogenic stimulators, which have an activating effect on
metabolic processes, particularly the general oxidation process in the
organism (cellular respiration). Constituents of placenta extracts are
amino acids and in particular peptides with hormone-like characters.
In Chrysocor, the content of potentially allergenic substances has
been strongly reduced by a special production process (low protein
content).

Application: Unless otherwise prescribed: 1 ampule of 2 ml to be injected intra


muscularly, 1-3 x weekly.

Side effects: Because of specific organic components of Chrysocor, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to foreign


protein.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 2 ml ampule 10 and 50 5X.

47
Citrokehl
Ampules
Liquid dilution for injection

Active ingredient: Acidum citricum 10X/30X/200X

Composition: 1 ampule of 2 ml contains: Medically active substance: 671 mg Acidum


citricum 10X aquous dil., 671 mg Acidum citricum 30X aquous
dil., 671 mg Acidum citricum 200X aquous dil. Other constituents:
isotonic sodium chloride solution.

According to experience, Allergic and rheumatic diseases; pneumonia and other respiratory dis-
to be administered in orders; arterial and venous diseases, arteriosclerosis; general symptoms,
cases of: e.g. tiredness, weather sensitivities, atypical headaches; gastrointestinal
dysfunction, cholangitis, dysbacteriosis, gastrointestinal complaints;
as adjuvant in pancreatic insufficiency; disorder of the acid-alkaline-
balance.

Characteristics: Acidum citricum (citric acid), the active ingredient of Citrokehl,


is an important link in the physiological citric acid cycle. It activates
cellular respiration and is of particular importance for cell metabolism.
Therefore, Citrokehl can be administered in all cases of illness.

Application: Unless otherwise prescribed: 1 ampule of 2 ml to be injected intra


muscularly 1-3 x weekly.
Children between the age of 6 and 12 years should not receive more
than 2/3 of the dosage for adults.

Side effects: None known.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 100 ml dropper bottle
10X/30X/ 200X potency mixture, 2 ml ampule 10 and 50 10X/30X/200X
mixed potency, 80 tablets 10X/30X/200X potency mixture.

48
Citrokehl
Drops
Liquid dilution
for oral intake

Active ingredient: Acidum citricum 10X/30X/200X

Composition: 100 ml liquid dilution contains: Medically active substance: 33.4 ml


Acidum citricum 10X dil., 33.4 ml Acidum citricum 30X dil., 33.4
ml Acidum citricum 200X dil. Other constituents: purified water,
ethanol.

According to experience, Allergic and rheumatic diseases; pneumonia and other respiratory dis-
to be administered in orders; arterial and venous diseases, arteriosclerosis; general symptoms,
cases of: e.g. tiredness, weather sensitivities, atypical headaches; gastrointestinal
dysfunction, cholangitis, dysbacteriosis, gastrointestinal complaints;
as adjuvant in pancreatic insufficiency; disorder of the acid-alkaline-
balance.

Characteristics: Acidum citricum (citric acid), the active ingredient of Citrokehl,


is an important link in the physiological citric acid cycle. It activates
cellular respiration and is of particular importance for cell metabolism.
Therefore, Citrokehl can be administered in all cases of illness.

Application: Unless otherwise prescribed: For oral intake: 1-3 x daily 5-20 drops.

Side effects: None known.

Contraindications: This product contains 50.6 % (v/v) alcohol (ethanol). This may present
a health risk in cases of liver diseases, alcoholism, epilepsy, brain
damage, pregnancy, and in children. The action of other drugs may be
reduced or intensified.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains 50.6 % (v/v) alcohol (ethanol).

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 100 ml dropper bottle
10X/30X/ 200X potency mixture, 2 ml ampule 10 and 50 10X/30X/200X
mixed potency, 80 tablets 10X/30X/200X potency mixture.

49
Citrokehl
Tablets
for oral intake

Active ingredient: Acidum citricum 10X/30X/200X

Composition: 1 tablet contains: Medically active substance: 83.34 mg Acidum


citricum 10X trit., 83.34 mg Acidum citricum 30X trit., 83.34
mg Acidum citricum 200X trit. Other constituents: lactose, potato
starch, magnesium stearate.

According to experience, Allergic and rheumatic diseases; pneumonia and other respiratory dis-
to be administered in orders; arterial and venous diseases, arteriosclerosis; general symptoms,
cases of: e.g. tiredness, weather sensitivities, atypical headaches; gastrointestinal
dysfunction, cholangitis, dysbacteriosis, gastrointestinal complaints;
as adjuvant in pancreatic insufficiency; disorder of the acid-alkaline-
balance.

Characteristics: Acidum citricum (citric acid), the active ingredient of Citrokehl,


is an important link in the physiological citric acid cycle. It activates
cellular respiration and is of particular importance for cell metabolism.
Therefore, Citrokehl can be administered in all cases of illness.

Application: Unless otherwise prescribed: 1-3 x daily 1-2 tablets.

Side effects: None known.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 100 ml dropper bottle
10X/30X/ 200X potency mixture, 2 ml ampule 10 and 50 10X/30X/200X
mixed potency, 80 tablets 10X/30X/200X potency mixture.

50
Cuprukehl 3X
Drops
Liquid dilution for oral intake

Active ingredient: Cuprum gluconicum 3X

Composition: 10 ml liquid dilution contain: Medically active substance: 0.8 ml Cuprum


gluconicum 3X dil. Other constituents: purified water, ethanol 15 %
(m/m).

According to experience, Inflammatory processes in the stomach, intestines and kidneys; pre- and
to be administered in postoperative phases.
cases of:

Characteristics: Copper is an essential trace element which is necessary in metabolism


for the function of diverse proteins and oxidative enzymes. It is
indispensable for the synthesis of hemoglobin, a healthy nerve function
and for bone formation. It also promotes the development of connective
tissue of the heart and circulatory system. Clinical situations which may
lead to a copper deficiency are premature births, patients supplied
entirely with parenteral nutrition and children living on substandard
nutrition. The capacity of the granulocytes for phagocytosis and the
formation of immunoglobulins are decreased by copper deficiency.

Application: Unless otherwise prescribed: For oral intake: in case of acute conditions
every half to one hour, not more than 6 times daily, each 5 drops. In case
of chronic conditions 1-3 x daily 5 drops.

Side effects: None known.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains 20 % (v/v) alcohol (ethanol). Due to the alcohol
content, professional medical advice should be sought prior to re
commending this product to patients with alcohol or liver problems.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 30 ml dropper bottle 3X, 2 ml
ampule 10 and 50 4X.

51
Cuprukehl 4X
Ampules
Liquid dilution for injection

Active ingredient: Cuprum gluconicum 4X

Composition: 1 ampule of 2 ml contains: Medically active substance: 2 ml


Cuprum gluconicum 4X aquous dil. Other constituents: isotonic
sodium chloride solution.

According to experience, Inflammatory processes in the stomach, intestines and kidneys; pre- and
to be administered in postoperative phases.
cases of:

Characteristics: Copper is an essential trace element which is necessary in metabolism


for the function of diverse proteins and oxidative enzymes. It is
indispensable for the synthesis of hemoglobin, a healthy nerve function
and for bone formation. It also promotes the development of connective
tissue of the heart and circulatory system. Clinical situations which may
lead to copper deficiency are premature births, patients supplied entirely
with parenteral nutrition and children living on substandard nutrition.
The capacity of the granulocytes for phagocytosis and the formation of
immunoglobulins are decreased by copper deficiency.

Application: Unless otherwise prescribed: 1 ampule of 2 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1-2
x daily.

Side effects: None known.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 30 ml dropper bottle 3X, 2 ml
ampule 10 and 50 4X.

52
Episcorit
Drops
Liquid dilution
for oral intake

Active ingredient: Concentrate of Echinacea purpurea with alcohol

Composition: 100 ml liquid dilution contain: Medically active substance: 75.6 ml


concentrate from fresh, blooming Echinacea purpurea herbs (1.5 -
2.5 : 1). Other constituents: ethanol.

According to experience, Support of treatment of recurrent infections of the respiratory and


to be administered in urinary tract.
cases of:

Characteristics: The origin of Echinacea purpurea is North America, where its wound
healing properties were preferred by the Indians. Echinacea stimulates
the production of endogenic interferon and therefore considerably
increases defensive mechanisms. Amongst others, they increase the
number of leucocytes and splenocytes.

Application: Unless otherwise prescribed: For oral intake: 3-4 x daily 55 drops.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Occasionally signs of a hypersensitivity reaction may occur. For drugs
containing Echinacea, symptoms like skin irritation, itching, facial
swelling, shortness of breath, dizziness, drop in blood pressure are
known. In this case, discontinue medication and treat symptomatically.

Contraindications: This preparation should not be administered if cases of hypersensitivity


against any of the ingredients, exipients or compositae are known.
Furthermore, it should not be administered in patients with progressive
systemic diseases such as tuberculosis, leucosis or similar diseases,
inflammatory diseases of the connective tissue (collagenosis), multiple
sclerosis, AIDS, HIV infections, other chronic viral illnesses and
autoimmune diseases.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains 22 % (v/v) alcohol (ethanol).


Due to the alcohol content, professional medical advice should be
sought prior to recommending this product to patients with alcohol or
liver problems.

53
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 30 ml and 100 ml dropper
bottle.

54
Exmykehl 3X
Suppositories
for rectal application

Active ingredients: Candida albicans e volumine cellulae (lyophil., steril.) 3X,


Candida parapsilosis e volumine cellulae (lyophil., steril.) 3X,
Penicillium roquefortii e volumine cellulae (lyophil., steril.) 3X

Composition: 1 suppository contains: Medically active substances: 0.067 g Candida


albicans e volumine cellulae (lyophil., steril.) 3X trit., 0.067 g
Candida parapsilosis e volumine cellulae (lyophil., steril.)
3X trit., 0.067 g Penicillium roquefortii e volumine cellulae
(lyophil., steril.) 3X trit. Other constituents: hard fat, lactose.

According to experience, Intestinal mycosis, vaginal mycosis; prostate hypertrophy.


to be administered in
cases of:

Characteristics: Exmykehl is a combination of three specific antimycotic preparations:


Candida albicans, Candida parapsilosis and Penicillium
roquefortii. The combination results in a broad spectrum of action.

Application: Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally.

Side effects: Because of specific organic components of Exmykehl theoretically,


hypersensitivity may occur In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Candida albicans, Candida parapsilosis and Penicillium
roquefortii).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Exmykehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X.

55
Exmykehl 5X
Ampules
Liquid dilution for injection

Active ingredients: Candida albicans e volumine cellulae (lyophil., steril.) 5X,


Candida parapsilosis e volumine cellulae (lyophil., steril.) 5X,
Penicillium roquefortii e volumine cellulae (lyophil., steril.)
5X

Composition: 1 ampule of 1 ml contains: Medically active substances: 0.334 ml


Candida albicans e volumine cellulae (lyophil., steril.) 5X
aquous dil., 0.334 ml Candida parapsilosis e volumine cellulae
(lyophil., steril.) 5X aquous dil., 0.334 ml Penicillium roquefortii
e volumine cellulae (lyophil., steril.) 5X aquous dil. Other
constituents: isotonic sodium chloride solution.

According to experience, Intestinal mycosis, vaginal mycosis; prostate hypertrophy.


to be administered in
cases of:

Characteristics: Exmykehl is a combination of three specific antimycotic preparations:


Candida albicans, Candida parapsilosis and Penicillium
roquefortii. The combination results in a broad spectrum of action.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected subcuta


neously, 1-3 x weekly.

Side effects: Because of specific organic components of Exmykehl theoretically,


hypersensitivity may occur In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Candida albicans, Candida parapsilosis and Penicillium
roquefortii).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Exmykehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X.

56
Exmykehl 5X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredients: Candida albicans e volumine cellulae (lyophil., steril.) 5X,


Candida parapsilosis e volumine cellulae (lyophil., steril.) 5X,
Penicillium roquefortii e volumine cellulae (lyophil., steril.)
5X

Composition: 10 ml liquid dilution contain: Medically active substance: 3.34 ml


Candida albicans e volumine cellulae (lyophil., steril.) 5X dil.,
3.34 ml Candida parapsilosis e volumine cellulae (lyophil.,
steril.) 5X dil, 3.34 ml Penicillium roquefortii e volumine cellulae
(lyophil., steril.) 5X dil. Other constituents: purified water.

According to experience, Intestinal mycosis, vaginal mycosis; prostate hypertrophy.


to be administered in
cases of:

Characteristics: Exmykehl is a combination of three specific antimycotic preparations:


Candida albicans, Candida parapsilosis and Penicillium
roquefortii. The combination results in a broad spectrum of action.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.

Side effects: Because of specific organic components of Exmykehl theoretically,


hypersensitivity may occur In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Candida albicans, Candida parapsilosis and Penicillium
roquefortii).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Exmykehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X.

57
Fomepikehl 5X
Ampules
Liquid dilution for injection

Active ingredient: Fomitopsis pinicola extractum e volumine ex muris cellulae


(lyophil., steril.) 5X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml


Fomitopsis pinicola extractum e volumine ex muris cellulae
5X aquous dil. Other constituents: isotonic sodium chloride solution.

According to experience, Intermittent, remittent and bilious fever with headache, yellow tongue,
to be administered in constant nausea, weakness in the upper abdomen and constipation;
cases of: prostate adenoma.

Characteristics: Polysaccarid extracts from Fomitopsis pinicola prove to be highly


effective immune modulators. They also have vasodilatory and
hypotensive properties.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected subcuta


neously, 1-3 x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Fomepikehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Fomitopsis


pinicola.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Fomepikehl.


with other remedies:

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X.

58
Fomepikehl 5X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Fomitopsis pinicola extractum e volumine ex muris cellulae


(lyophil., steril.) 5X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Fomitopsis pinicola extractum e volumine ex muris cellulae
(lyophil., steril.) 5X dil. Other constituents: purified water.

According to experience, Intermittent, remittent and bilious fever with headache, yellow tongue,
to be administered in constant nausea, weakness in the upper abdomen and constipation;
cases of: prostate adenoma.

Characteristics: Polysaccarid extracts from Fomitopsis pinicola prove to be highly


effective immune modulators. They also have vasodilatory and
hypotensive properties.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Fomepikehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Fomitopsis


pinicola.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Fomepikehl.


with other remedies:

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X.

59
Formasan
Ampules
Liquid dilution for injection

Active ingredient: Acidum formicicum 6X/12X/30X/200X

Composition: 1 ampule of 2 ml contains: Medically active substance: 0.5 ml Acidum


formicicum 6X aquous dil., 0.5 ml Acidum formicicum 12X
aquous dil., 0.5 ml Acidum formicicum 30X aquous dil., 0.5 ml
Acidum formicicum 200X aquous dil. Other constituents: isotonic
sodium chloride solution.

According to experience, Rheumatism of the muscles and joints; eczema; bronchial asthma,
to be administered in allergies.
cases of:

Characteristics: Acidum formicicum (formic acid), the active ingredient of Formasan,


is traditionally used in folk medicine as embrocation in cases of
arthrosis, arthritis and rheumatism. Todays priority is the treatment of
rheumatic diseases with allergic diathesis. In homeopathy, ant acid is a
highly effective constitutional preparation for uric acid, rheumatic and
allergic conditions.

Application: Unless otherwise prescribed: 1 ampule of 2 ml to be injected intra


muscularly or subcutaneously, 1-3 x weekly.

Side effects: None known.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 100 ml dropper bottle 6X/12X/
30X/200X potency mixture, 2 ml ampule 10 and 50 6X/12X/30X/200X
potency mixture.

60
Formasan 6X/12X/30X/200X
Drops
Liquid dilution for oral intake

Active ingredient: Acidum formicicum 6X/12X/30X/200X

Composition: 1 ml liquid dilution contains: Medically active substance: 0.25 ml Acidum


formicicum 6X dil., 0.25 ml Acidum formicicum 12X dil., 0.25 ml
Acidum formicicum 30X dil., 0.25 ml Acidum formicicum 200X
dil. Other constituents: Other constituents: purified water, ethanol.

According to experience, Rheumatism of the muscles and joints; eczema; bronchial asthma;
to be administered in allergies.
cases of:

Characteristics: Acidum formicicum (formic acid), the active ingredient of Formasan,


is traditionally used in folk medicine as embrocation in cases of
arthrosis, arthritis and rheumatism. Todays priority is the treatment of
rheumatic diseases with allergic diathesis. In homeopathy, ant acid is a
highly effective constitutional preparation for uric acid, rheumatic and
allergic conditions.

Application: Unless otherwise prescribed: For oral intake: 1-3 x daily 5-20 drops.

Side effects: None known.

Contraindications: This product contains 50.6 % (v/v) alcohol (ethanol). This may present
a health risk in cases of liver diseases, alcoholism, epilepsy, brain
damage, pregnancy, and in children. The action of other drugs may be
reduced or intensified.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains 50.6 % (v/v) alcohol (ethanol).

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 100 ml dropper bottle 6X/12X/
30X/200X potency mixture, 2 ml ampule 10 and 50 6X/12X/30X/200X
potency mixture.

61
Fortakehl 3X
Suppositories
for rectal application

Active ingredient: Penicillium roquefortii e volumine cellulae (lyophil., steril.) 3X

Composition: 1 suppository contains: Medically active substance: 0.2 g Penicillium


roquefortii e volumine cellulae (lyophil., steril.) 3X trit. Other
constituents: hard fat, lactose.

According to experience, Dysbacteria and destroyed mucosa, gastritis, enteritis, colitis syndrome
to be administered in, pancreatitis, diarrhea, constipation, vomitus, gastric ulcer; mycoses of the
cases of: intestine, the vagina and the skin; bronchitis, susceptibility to
infections.

Characteristics: Fortakehl is obtained from the mold fungus Penicillium roquefortii;


it is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damage, destruction
of the intestinal flora, and the formation of penicillin-resistant strains.

Application: Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally.

Side effects: Because of specific organic components of Fortakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Penicillium roquefortii).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Fortakehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.


Penicillium roquefortii as an active ingredient is also contained in
Exmykehl.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1
ml ampule 10 and 50 5X, 6X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.

62
Fortakehl 4X
Capsules
for oral intake

Active ingredient: Penicillium roquefortii e volumine cellulae (lyophil., steril.) 4X

Composition: 1 capsule contains: Medically active substance: 330 mg Penicillium


roquefortii e volumine cellulae (lyophil., steril.) 4X trit. Other
constituents: lactose, hypromellosis (capsule shell).

According to experience, Dysbacteria and destroyed mucosa, gastritis, enteritis, colitis syndrome,
to be administered in pancreatitis, diarrhea, constipation, vomitus, gastric ulcer; mycoses of the
cases of: intestine, the vagina and the skin; bronchitis, susceptibility to infections.

Characteristics: Fortakehl is obtained from the mold fungus Penicillium roquefortii;


it is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damage, destruction
of the intestinal flora, and the formation of penicillin-resistant strains.

Application: Unless otherwise prescribed: 1-3 x daily 1 capsule.

Side effects: Because of specific organic components of Fortakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Penicillium roquefortii).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Fortakehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.


Penicillium roquefortii as an active ingredient is also contained in
Exmykehl.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1
ml ampule 10 and 50 5X, 6X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.

63
Fortakehl 5X
Ampules
Liquid dilution for injection

Active ingredient: Penicillium roquefortii e volumine cellulae (lyophil., steril.) 5X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Penicillium


roquefortii e volumine cellulae (lyophil., steril.) 5X aquous dil.
Other constituents: isotonic sodium chloride solution.

According to experience, Dysbacteria and destroyed mucosa, gastritis, enteritis, colitis syndrome,
to be administered in pancreatitis, diarrhea, constipation, vomitus, gastric ulcer; mycoses of the
cases of: intestine, the vagina and the skin; bronchitis, susceptibility to
infections.

Characteristics: Fortakehl is obtained from the mold fungus Penicillium roquefortii;


it is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damage, destruction
of the intestinal flora, and the formation of penicillin-resistant strains.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


subcutaneously or intracutaneously, 1-3 x weekly.

Side effects: Because of specific organic components of Fortakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Penicillium roquefortii).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Fortakehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: Penicillium roquefortii as an active ingredient is also contained in


Exmykehl.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1
ml ampule 10 and 50 5X, 6X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.

64
Fortakehl 5X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Penicillium roquefortii e volumine cellulae (lyophil., steril.) 5X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Penicillium roquefortii e volumine cellulae (lyophil., steril.)
5X dil. Other constituents: purified water.

According to experience, Dysbacteria and destroyed mucosa, gastritis, enteritis, colitis syndrome,
to be administered in pancreatitis, diarrhea, constipation, vomitus, gastric ulcer; mycoses of
cases of: the intestine, the vagina and the skin; bronchitis, susceptibility to
infections.

Characteristics: Fortakehl is obtained from the mold fungus Penicillium roquefortii;


it is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damage, destruction
of the intestinal flora, and the formation of penicillin-resistant strains.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.

Side effects: Because of specific organic components of Fortakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Penicillium roquefortii).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Fortakehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: After opening, contents must be used within two months. Penicillium
roquefortii as an active ingredient is also contained in Exmykehl.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1
ml ampule 10 and 50 5X, 6X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.

65
Fortakehl 5X
Tablets
for oral intake

Active ingredient: Penicillium roquefortii e volumine cellulae (lyophil., steril.) 5X

Composition: 1 tablet contains: Medically active substance: 250 mg Penicillium


roquefortii e volumine cellulae (lyophil., steril.) 5X trit. Other
constituents: lactose, potato starch, magnesium stearate.

According to experience, Dysbacteria and destroyed mucosa, gastritis, enteritis, colitis syndrome,
to be administered in pancreatitis, diarrhea, constipation, vomitus, gastric ulcer; mycoses of
cases of: the intestine, the vagina and the skin; bronchitis, susceptibility to
infections.

Characteristics: Fortakehl is obtained from the mold fungus Penicillium roquefortii;


it is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damage, destruction
of the intestinal flora, and the formation of penicillin-resistant strains.

Application: Unless otherwise prescribed: 1-3 x daily 1 tablet.

Side effects: Because of specific organic components of Fortakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Penicillium roquefortii).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Fortakehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.


Penicillium roquefortii as an active ingredient is also contained in
Exmykehl.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1
ml ampule 10 and 50 5X, 6X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.

66
Fortakehl 6X
Ampules
Liquid dilution for injection

Active ingredient: Penicillium roquefortii e volumine cellulae (lyophil., steril.) 6X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Penicillium


roquefortii e volumine cellulae (lyophil., steril.) 6X aquous dil.
Other constituents: isotonic sodium chloride solution.

According to experience, Dysbacteria and destroyed mucosa, gastritis, enteritis, colitis syndrome,
to be administered in pancreatitis, diarrhea, constipation, vomitus, gastric ulcer; mycoses of
cases of: the intestine, the vagina and the skin; bronchitis, susceptibility to
infections.

Characteristics: Fortakehl is obtained from the mold fungus Penicillium roquefortii;


it is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damage, destruction
of the intestinal flora, and the formation of penicillin-resistant strains.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected subcuta


neously, 1-3 x weekly.

Side effects: Because of specific organic components of Fortakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Penicillium roquefortii).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Fortakehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: Penicillium roquefortii as an active ingredient is also contained in


Exmykehl.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1
ml ampule 10 and 50 5X, 6X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.

67
Ginkgobakehl 1X
Drops
Liquid dilution
for oral intake

Active ingredient: Ginkgo biloba e foliis sicc. mother tincture

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Ginkgo


biloba e foliis sicc. 1X dil. Other constituents: purified water, ethanol
62.4 % (m/m).

According to experience, According to the homeopathic drug picture, e.g. circulatory disorders
to be administered in (arterial and peripheral), arteriosclerosis; weakness in concentration,
cases of: tiredness.

Characteristics: In China Ginkgo preparations are known for treatment of various


diseases such as circulating disorders, various toxic burdens since
3,000 years B.C.

Application: Unless otherwise prescribed: For oral intake: 3-5 x daily 10-15 drops.

Side effects: Because of specific organic components of Ginkgobakehl, theo


retically, hypersensitivity may occur. In this case, discontinue medication
and treat symptomatically.
In very rare cases the following symptoms were observed: gastrointestinal
complaints, fever, headaches or allergic skin reactions (reddening,
swelling, itching). In cases of long-term treatment occasionally bleeding
occurred, however, a causal link to the intake of Ginkgo preparations
has not been verified.

Contraindications: This product contains 70 % (v/v) alcohol (ethanol). Following the dosage
recommendations, 15 drops lead to an alcohol intake of 0.2 g. This may
present a health risk in cases of liver diseases, alcoholism, epilepsy,
brain damage, pregnancy, and in children. The action of other drugs
may be reduced or intensified.

Adverse reactions: None known.

Interactions The action of anticoagulants may be intensified. Please note that this also
with other remedies: applies to intake a few hours or days before.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains 70 % (v/v) alcohol (ethanol).

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 30 ml dropper bottle 1X, 4X,
2 ml ampule 10 and 50 4X.

68
Ginkgobakehl 4X
Ampules
Liquid dilution for injection

Active ingredient: Ginkgo biloba e foliis sicc. 4X

Composition: 1 ampule of 2 ml contains: Medically active substance: 2 ml Ginkgo


biloba e foliis sicc. 4X aquous dil. Other constituents: isotonic
sodium chloride solution.

According to experience, According to the homeopathic drug picture, e.g. circulatory disorders
to be administered in (arterial and peripheral), arteriosclerosis; weakness in concentration,
cases of: tiredness.

Characteristics: In China Ginkgo preparations are known for treatment of various


diseases such as circulating disorders, various toxic burdens since
3,000 years B.C.

Application: Unless otherwise prescribed: 1 ampule of 2 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1 x
daily.

Side effects: Because of specific organic components of Ginkgobakehl, theo


retically, hypersensitivity may occur. In this case, discontinue medication
and treat symptomatically.
In very rare cases the following symptoms were observed: gastrointestinal
complaints, fever, headaches or allergic skin reactions (reddening,
swelling, itching). In cases of long-term treatment occasionally bleeding
occurred, however, a causal link to the intake of Ginkgo preparations
has not been verified.

Contraindications: Do not administer in cases of known hypersensitivity to Ginkgo biloba.

Adverse reactions: None known.

Interactions The action of anticoagulants may be intensified. Please note that this
with other remedies: also applies to intake a few hours or days before.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 30 ml dropper bottle 1X, 4X,
2 ml ampule 10 and 50 4X.

69
Ginkgobakehl 4X
Drops
Liquid dilution
for oral intake

Active ingredient: Ginkgo biloba e foliis sicc. 4X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Ginkgo


biloba e foliis sicc. 4X dil. Other constituents: purified water, ethanol
42.4 % (m/m).

According to experience, According to the homeopathic drug picture, e.g. circulatory disorders
to be administered in (arterial and peripheral), arteriosclerosis; weakness in concentration,
cases of: tiredness.

Characteristics: In China Ginkgo preparations are known for treatment of various


diseases such as circulating disorders, various toxic burdens since
3,000 years B.C.

Application: Unless otherwise prescribed: For oral intake: 3-5 x daily 10-15 drops.

Side effects: Because of specific organic components of Ginkgobakehl, theo


retically, hypersensitivity may occur. In this case, discontinue medication
and treat symptomatically.
In very rare cases the following symptoms were observed: gastrointestinal
complaints, fever, headaches or allergic skin reactions (reddening,
swelling, itching). In cases of long-term treatment occasionally bleeding
occurred, however, a causal link to the intake of Ginkgo preparations
has not been verified.

Contraindications: This product contains 50 % (v/v) alcohol (ethanol). Following the dosage
recommendations, 15 drops lead to an alcohol intake of 0.2 g. This may
present a health risk in cases of liver diseases, alcoholism, epilepsy,
brain damage, pregnancy, and in children. The action of other drugs
may be reduced or intensified.

Adverse reactions: None known.

Interactions The action of anticoagulants may be intensified. Please note that this
with other remedies: also applies to intake a few hours or days before.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains 50 % (v/v) alcohol (ethanol).

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 30 ml dropper bottle 1X, 4X,
2 ml ampule 10 and 50 4X.

70
Grifokehl 5X
Ampules
Liquid dilution for injection

Active ingredient: Grifola frondosa e volumine cellulae (lyophil., steril.) 5X

Composition: 1 ampule of 1 ml contains:: Medically active substance: 10 ml Grifola


frondosa e volumine cellulae (lyophil., steril.) 5X dil. Other
constituents: isotonic sodium chloride solution.

According to experience, Immune modulation, Herpes simplex, Herpes zoster.


to be administered in
cases of:

Characteristics: Grifokehl is produced from parts of the Grifola frondosa fungus which
is known as Maitake in Japan. It can be characterised as an adaptogen,
i.e. it has a compensatory effect independent from the cause of the
disease. Investigations in Japan revealed an inhibiting effect on tumor
growth which is based on enhanced cell mediated immune defense.
This mechanism is also responsible for the antiviral activity of the
fungus. Furthermore, it was shown that Grifola frondosa has lowering
effects on blood pressure and blood glucose.
It is important to use extracts from the fruiting bodies of the fungus in
order to obtain these effects.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3 x
weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Grifokehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Grifola


frondosa.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X.

71
Grifokehl 5X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Grifola frondosa e volumine cellulae (lyophil., steril.) 5X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Grifola


frondosa e volumine cellulae (lyophil., steril.) 5X dil. Other
constituents: purified water.

According to experience, Immune modulation, Herpes simplex, Herpes zoster.


to be administered in
cases of:

Characteristics: Grifokehl is produced from parts of the Grifola frondosa fungus which
is known as Maitake in Japan. It can be characterised as an adaptogen,
i.e. it has a compensatory effect independent from the cause of the
disease. Investigations in Japan revealed an inhibiting effect on tumor
growth which is based on enhanced cell mediated immune defense.
This mechanism is also responsible for the antiviral activity of the
fungus. Furthermore, it was shown that Grifola frondosa has lowering
effects on blood pressure and blood glucose.
It is important to use extracts from the fruiting bodies of the fungus in
order to obtain these effects.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Grifokehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Grifola


frondosa.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X.

72
Hexacyl
Drops
Liquid dilution
for oral intake

Active ingredients: Sulphur 4X dilution, Lycopodium clavatum mother tincture,


Berberis vulgaris mother tincture

Composition: 10 g (corresponds to 10.99 ml) liquid dilution contains: Medically active


substance: 3.00 g Sulphur 4X dil, 0.10 g Lycopodium clavatum
mother tincture, 0.05 g Berberis vulgaris mother tincture.
Other constituents:, ethanol 43% (m/m), purified water.

Indication Supporting treatment for functional liver, gallbladder and kidney


disorders.

Characteristics: The active ingredients of Hexacyl - Sulphur, Lycopodium clavatum


and Berberis vulgaris - present a similar range of action in their
homeopathic drug picture. Each of the single substances shows
symptoms of venous stasis in the circulatory system which results in
disturbances of other organs, in particular of the liver and kidneys.
Leading symptoms are: Severe burning and itching, exhaustion;
deterioration by heat, cold and rest; improvement through fresh air and
moderate movement. Hexacyl is indicated for elimination of all toxic
or infectious damage with increased degradation of protein such as
food intolerance, infections and intoxications.

Application: Unless otherwise prescribed:


For oral intake: in case of acute conditions 5 drops every half to full
hour up to a maximum of 12 times daily. In case of chronic conditions 5
drops up to 3 times daily.

Side effects: Because of the specific organic components of Hexacyl, theoretically,


hypersensitivity may occur. In this case, discontinue use and treat
symptomatically.

Contraindications: This product contains 59.9 % (v/v) alcohol (ethanol). This may present
a health risk in cases of liver diseases, alcoholism, epilepsy, brain
damage, pregnancy, and in children. The action of other drugs may be
reduced or intensified.

Adverse reactions: None known.

Interactions,
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains 59.9 % (v/v) alcohol (ethanol).

73
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage form is available: 30 ml dropper bottle.

74
Larifikehl 4X
Capsules
for oral intake

Active ingredient: Laricifomes officinalis e volumine cellulae (lyophil., steril.)


4X

Composition: 1 capsule contains: Medically active substance: 330 mg Laricifomes


officinalis e volumine cellulae (lyophil., steril.) 4X trit. Other
constituents: lactose, hypromellosis (capsule shell).

According to experience, Fever, lung diseases and inflammation of the digestive organs; primary
to be administered in chronic polyarthritis.
cases of:

Characteristics: Larifikehl is produced from the fungus Laricifomes officinalis. In


popular medicine, it has been used predominantly for treatment of night
sweat in lung diseases, of asthma, cough, and also as a laxative.

Application: Unless otherwise prescribed: 1-3 x daily 1 capsule.


Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Larifikehl, theoretically,


hypersensitivity may occur, mainly in the form of skin reactions. Also
allergic reactions against the ingredient Laricifomes officinalis
are possible. In this case, discontinue medication and treat sympto
matically.

Contraindications: Do not administer in cases of known hypersensitivity to Laricifomes


officinalis.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of with other


remedies: Larifikehl. An interval of 4 weeks before and after the
treatment with orally administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 20 capsules 4X.

75
Larifikehl 5X
Ampules
Liquid dilution for injection

Active ingredient: Laricifomes officinalis e volumine cellulae (lyophil., steril.)


5X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Laricifomes


officinalis e volumine cellulae (lyophil., steril.) 5X aquous dil.
Other constituents: isotonic sodium chloride solution.

According to experience, Fever, lung diseases and inflammation of the digestive organs; primary
to be administered in chronic polyarthritis.
cases of:

Characteristics: Larifikehl is produced from the fungus Laricifomes officinalis. In


popular medicine, it has been used predominantly for treatment of night
sweat in lung diseases, of asthma, cough, and also as a laxative.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3 x
weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Larifikehl, theoretically,


hypersensitivity may occur, mainly in the form of skin reactions. Also
allergic reactions against the ingredient Laricifomes officinalis
are possible. In this case, discontinue medication and treat sympto
matically.

Contraindications: Do not administer in cases of known hypersensitivity to Laricifomes


officinalis.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Larifikehl.


with other remedies: An interval of 4 weeks before and after the treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 20 capsules 4X.

76
Larifikehl 5X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Laricifomes officinalis e volumine cellulae (lyophil., steril.)


5X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Laricifomes officinalis e volumine cellulae (lyophil., steril.)
5X dil. Other constituents: purified water.

According to experience, Fever, lung diseases and inflammation of the digestive organs; primary
to be administered in chronic polyarthritis.
cases of:

Characteristics: Larifikehl is produced from the fungus Laricifomes officinalis. In


popular medicine, it has been used predominantly for treatment of night
sweat in lung diseases, of asthma, cough, and also as a laxative.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.

Side effects: Because of specific organic components of Larifikehl, theoretically,


hypersensitivity may occur, mainly in the form of skin reactions. Also
allergic reactions against the ingredient Laricifomes officinalis
are possible. In this case, discontinue medication and treat sympto
matically.

Contraindications: Do not administer in cases of known hypersensitivity to Laricifomes


officinalis.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Larifikehl.


with other remedies: An interval of 4 weeks before and after the treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 20 capsules 4X.

77
Latensin 4X
Ampules
Liquid dilution for injection

Active ingredient: Bacillus cereus e volumine cellulae (lyophil. steril.) 4X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Bacillus


cereus e volumine cellulae (lyophil., steril.) 4X aquous dil. Other
constituents: isotonic sodium chloride solution.

According to experience, Chronic inflammation of the respiratory and digestive tract; chronic
to be administered in rheumatic disorders; chronic skin diseases; susceptibility to infection
cases of: (for immune modulation).

Characteristics: Latensin is produced from the non-pathogenic microbe Bacillus


cereus. It is applied for immune modulation, especially in chronic
infections.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously or intracutaneously, 1-2 x weekly.

Side effects: Because of specific organic components of Latensin, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


Do not administer in cases of known hypersensitivity to Bacillus
cereus.

Adverse reactions: None known. Generally well tolerated. Occasionally local reactions
like rubefaction, swelling or painfulness may be observed, normally
vanishing without treatment. These effects are not to be seen as
adverse reactions, but rather as an expression of effectiveness. In the
first 2 or 3 days after the injection sometimes conditions of weakness,
fortified expectoration, slight painfulness of the region or subfebrile
temperatures may show. Strong general reactions are always a sign of
overdose or of incorrect injection technique.

Interactions Immunosuppressive drugs can influence the effectivity of Latensin.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X,6X.

78
Latensin 4X
Capsules
for oral intake

Active ingredient: Bacillus cereus e volumine ex muris cellulae (lyophil., steril.)


4X

Composition: 1 capsule contains: Medically active substance: 330 mg Bacillus


cereus e volumine ex muris cellulae (lyophil., steril.) 4X trit.
Other constituents: lactose, hypromellosis (capsule shell).

According to experience, Chronic inflammation of the respiratory and digestive tract; chronic
to be administered in rheumatic disorders; chronic skin diseases; susceptibility to infection
cases of: (for immune modulation).

Characteristics: Latensin is produced from the non-pathogenic microbe Bacillus


cereus. It is applied for immune modulation, especially in chronic
infections.

Application: Unless otherwise prescribed: 1-2 x weekly 1 capsule.

Side effects: Because of specific organic components of Latensin, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


Do not administer in cases of known hypersensitivity to Bacillus
cereus.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Latensin.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X,6X.

79
Latensin 6X
Ampules
Liquid dilution for injection

Active ingredient: Bacillus cereus e volumine cellulae (lyophil., steril.) 6X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Bacillus


cereus e volumine cellulae (lyophil., steril.) 6X aquous dil. Other
constituents: isotonic sodium chloride solution.

According to experience, Chronic inflammation of the respiratory and digestive tract; chronic
to be administered in rheumatic disorders; chronic skin diseases; susceptibility to infection
cases of: (for immune modulation).

Characteristics: Latensin is produced from the non-pathogenic microbe Bacillus


cereus. It is applied for immune modulation, especially in chronic
infections.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously or intracutaneously, 1-2 x weekly.

Side effects: Because of specific organic components of Latensin, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


Do not administer in cases of known hypersensitivity to Bacillus
cereus.

Adverse reactions: None known. Generally well tolerated. Occasionally local reactions
like rubefaction, swelling or painfulness may be observed, normally
vanishing without treatment. These effects are not to be seen as
adverse reactions, but rather as an expression of effectiveness. In the
first 2 or 3 days after the injection sometimes conditions of weakness,
fortified expectoration, slight painfulness of the region or subfebrile
temperatures may show. Strong general reactions are always a sign of
overdose or of incorrect injection technique.

Interactions Immunosuppressive drugs can influence the effectivity of Latensin.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X,6X.

80
Latensin 6X
Capsules
for oral intake

Active ingredient: Bacillus cereus e volumine ex muris cellulae (lyophil., steril.)


6X

Composition: 1 capsule contains: Medically active substance: 330 mg Bacillus


cereus e volumine ex muris cellulae (lyophil., steril.) 6X trit.
Other constituents: lactose, hypromellosis (capsule shell).

According to experience, Chronic inflammation of the respiratory and digestive tract; chronic
to be administered in rheumatic disorders; chronic skin diseases; susceptibility to infection
cases of: (for immune modulation).

Characteristics: Latensin is produced from the non-pathogenic microbe Bacillus


cereus. It is applied for immune modulation, especially in chronic
infections.

Application: Unless otherwise prescribed: 1-2 x weekly 1 capsule.

Side effects: Because of specific organic components of Latensin, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


Do not administer in cases of known hypersensitivity to Bacillus
cereus.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Latensin.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

81
Latensin 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Bacillus cereus e volumine cellulae (lyophil., steril.) 6X

Composition: 5 ml liquid dilution contain: Medically active substance: 5 ml Bacillus


cereus e volumine cellulae (lyophil., steril.) 6X dil. Other
constituents: purified water.

According to experience, Chronic inflammation of the respiratory and digestive tract; chronic
to be administered in rheumatic disorders; chronic skin diseases; susceptibility to infection
cases of: (for immune modulation).

Characteristics: Latensin is produced from the non-pathogenic microbe Bacillus


cereus. It is applied for immune modulation, especially in chronic
infections.

Application: Unless otherwise prescribed: For oral intake: 1-3 x weekly 2-5. For
rubbing in: 1-3 x weekly 2-5 drops into the bend of the elbow.

Side effects: Because of specific organic components of Latensin, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.

Do not apply to inflamed skin. Do not administer in cases of known


hypersensitivity to Bacillus cereus.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Latensin.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

82
Latensin 6X
Suppositories
for rectal application

Active ingredient: Bacillus cereus e volumine ex muris cellulae (lyophil., steril.) 6X

Composition: 1 suppository contains: Medically active substance: 0.2 g Bacillus


cereus e volumine ex muris cellulae (lyophil., steril.) 6X trit.
Other constituents: hard fat, lactose.

According to experience, Chronic inflammation of the respiratory and digestive tract; chronic
to be administered in rheumatic disorders; chronic skin diseases; susceptibility to infection
cases of: (for immune modulation).

Characteristics: Latensin is produced from the non-pathogenic microbe Bacillus


cereus. It is applied for immune modulation, especially in chronic
infections.

Application: Unless otherwise prescribed: 1-3 x weekly insert 1 suppository rectally.

Side effects: Because of specific organic components of Latensin, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


Do not administer in cases of known hypersensitivity to Bacillus
cereus.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Latensin.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

83
Leptospermusan 1X
Drops
Liquid dilution
for oral intake

Active ingredient: Leptospermum scoparium e apic. ramorum siccum 1X

Composition: 1 ml liquid dilution contain: Medically active substance: 1 ml


Leptospermum scoparium e apic. ramorum siccum 1X dil.
Other constituents: purified water, ethanol.

According to experience, Secondary effects of apoplexy, ischaemic attack; inflammations such as


to be administered in trigeminal neuralgia, iritis, allergic conjunctivitis; diseases of the respiratory
cases of: tract such as cold and sore throat; for a general soothing influence;
sleep disorder; cell renewal; gastrointestinal diseases such as gastritis,
pylorospasm, constipation, colitis.

Characteristics: Leptospermum scoparium or manuka is a wild growing bush


found in New Zealand and is well known in Polynesian folk medicine.
Preparations from its leaves, bark and seed pods were used for
treating different diseases, but especially for dysentery and diarrhoea.
As with other species of the myrtles, Leptospermum scoparium
contains essential oils, well known for their antibacterial activity.
Anthelmintic properties of Leptospermum have been reported.
Further pharmacological effective constituents are tannins as well as
rare flavonoids.

Application: Unless otherwise prescribed: in case of acute conditions 5 drops every


half to full hour up to a maximum of 12 times daily. In case of chronic
conditions 5 drops up to 3 times daily.

Side effects: Because of specific organic components of Leptospermusan,


theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.

Contraindications: This product contains 70 % (v/v) alcohol (ethanol). This may present
a health risk in cases of liver diseases, alcoholism, epilepsy, brain
damage, pregnancy, and in children. The action of other drugs may be
reduced or intensified.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains 70 % (v/v) alcohol (ethanol).

84
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 30 ml dropper bottle 1X.

85
Leptucin 6X
Capsules
for oral intake

Active ingredient: Propionibacterium avidum e volumine ex muris cellulae


(lyophil., steril.) 6X

Composition: 1 capsule contains: Medically active substance: 330 mg Propioni


bacterium avidum e volumine ex muris cellulae (lyophil.,
steril.) 6X trit. Other constituents: lactose, hypromellosis (capsule
shell).

According to experience, Stimulation of circulation of the extremities; vascular migraine; tinnitus;


to be administered in inflammation of the urinary bladder; immune modulation.
cases of:

Characteristics: Propionibacteria belong to the strongest immune modulators. Due


to the special structure of their cell wall they are able to stimulate
the immune system by activation of the monocyte-macrophage-
system. They have antibacterial, antiviral, antiparasitic, and antitumor
properties. Moreover, Leptucin is a potent remedy for stimulation of
the circulatory system especially in the head and extremities.

Application: Unless otherwise prescribed: 1-2 x weekly 1 capsule.

Side effects: Because of specific organic components of Leptucin, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Propioni


bacterium avidum.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Leptucin.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 20 capsules 6X, 10
suppositories 6X.

86
Leptucin 6X
Suppositories
for rectal application

Active ingredient: Propionibacterium avidum e volumine ex muris cellulae


(lyophil., steril.) 6X

Composition: 1 suppository contains: Medically active substance: 0.2 g Bacillus


subtilis e volumine ex muris cellulae cellulae (lyophil., steril.)
6X trit. Other constituents: hard fat, lactose.

According to experience, Stimulation of circulation of the extremities; vascular migraine; tinnitus;


to be administered in inflammation of the urinary bladder; immune modulation.
cases of:

Characteristics: Propionibacteria belong to the strongest immune modulators. Due


to the special structure of their cell wall they are able to stimulate
the immune system by activation of the monocyte-macrophage-
system. They have antibacterial, antiviral, antiparasitic, and antitumor
properties. Moreover, Leptucin is a potent remedy for stimulation of
the circulatory system especially in the head and extremities.

Application: Unless otherwise prescribed: 1-3 x weekly insert 1 suppository rectally.

Side effects: Because of specific organic components of Leptucin, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Propioni


bacterium avidum.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Leptucin.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 20 capsules 6X, 10
suppositories 6X.

87
Lipiscor
Capsules
for oral intake

Active ingredient: Piscis oleum (polyunsaturated fatty acids from sea fish)

Composition: 1 Capsule contains: Medically active substance: 500 mg Piscis


oleum (polyunsaturated fatty acids from sea fish) containing
70 mg icosapent and 50 mg doconexent. Other constituents: RRR-a-
tocopherol, al-rac-a-tocopherolum acetate, gelatin, glycerol, purified
water.

Indication: To lower a highly increased triglyceride blood level. Lipiscor should


only be administered additionally if a diet is insufficient in lowering
triglyceride.

Characteristics: Lipiscor contains natural fish oil with a high content of essential
polyunsaturated omega-3-(n-3) fatty acids, which are icosapent
(eicosapentaenoic acid) and doconexent (docosahexaenoic acid).
The results of epidemiological studies on populations such as Innuits,
Japanese, Dutch and Americans show a correlation between a high
intake of sea fish and a low appearance of cardiovascular diseases. The
regular intake of Lipiscor leads to a lowering of plasma triglycerides
within four weeks. If taken on a permanent basis the triglyceride
level will remain constant. If discontinued, the plasma triglycerides
will return to their former level within 2-3 months. The omega-3 fatty
acids contained in Lipiscor go into the normal lipid metabolism,
particularly the metabolism of eicosanoids and prostaglandins. The
lipid-lowering effect of Lipiscor is probably the result of an inhibition
of the triglyceride synthesis. Taking Lipiscor increases the proportion
of omega-3-(n-3) fatty acids.

Application: Unless otherwise prescribed: 5-10 capsules twice daily. Lipiscor is to


be swallowed unchewed with some liquid before a meal.

Side effects: High dosages may occasionally cause nausea and eructation. Lipiscor
may prolong bleeding time and inhibit platelet aggregation. A modest
increase in transaminases is possible.

Contraindications: Acute and subacute pancreatitis, acute pancreas necrosis, acute and
chronic liver intoxications, cirrhosis of the liver from all origins, acute
to chronic cholecystitis, suppuration of the gall bladder, disorders of
digestion as well as emulsification of fat in the small intestine due to
diseases of the gallbladder and/or pancreas, thrombopathia, if allergic
reactions against any of the ingredients are known.
Because Lipiscor may cause a delay of uterine contractions it should
not be administered in the last 3 months of pregnancy.

Adverse reactions: In case of bronchial asthma which is sensitive to salicylic acid a


deterioration of the lung function may occur.

88
Interactions Since Lipiscor prolongs bleeding time and may reduce the platelet
with other remedies: aggregation, patients with thrombopenia and patients who are treated
with anticoagulant drugs should be under constant medical supervision
as it might be necessary to reduce the administration of anticoagulant
drugs.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children or in case of hypercholesterinaemia.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health careprofessional.

How supplied: The following dosage forms are available: 60 and 240 capsules.

89
Luffasan 4X
Tablets
for oral intake

Active ingredient: Luffa operculata 4X

Composition: 1 tablet contains: Medically active substance: 250 mg Luffa oper


culata 4X trit. Other constituents: lactose, potato starch, magnesium
stearate.

Indication: Hay fever, cold; headache, dyspepsia.

Characteristics: Luffasan is produced from the ripe, dried fruits of Luffa operculata
(related to the pumpkin family) and is a universal remedy in Brazils
folk medicine for constipation, oedemas and tumours. Luffasan is
predominantly used as a decongestant in cases of blockages caused
by inflammation.

Application: Unless otherwise prescribed: For oral intake: in case of acute conditions
1 tablet every half to full hour up to a maximum of 12 times daily. In case
of chronic conditions 2 tablets daily.

Side effects: Because of the specific organic components of Luffasan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Luffa oper


culata.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 80 tablets 4X.

90
Mapurit L
Capsules
for oral intake

Active ingredients: Magnesium oxide, vitamin E

Composition: 1 capsule contains: 208,4 mg magnesium oxide, 123,5 mg vitamin E


(as RRR-alpha-tocopherylhydrogensuccinat). Other constituents: hypro
mellose, cellulose, magnesiumstearat.

From experience Reduced endogenous resistibility, especially chronic exhaustion.


to administer for:

Characteristics: Magnesium deficiency is an important diet-related cause for the


development of chronic exhaustion. To compensate, magnesium oxide
should be administered which has a membrane-stabilizing effect on all
cell membranes and cell organelle membranes. The metabolism of carbo
hydrates, proteins and lipids as well as the excitation metabolism of
nerves and muscles are positively affected.

Application: Recommended dose: 1 capsule twice a day.

How supplied: Package with 40/100 capsules.

91
Mucedokehl 3X
Suppositories
for rectal application

Active ingredient: Mucor mucedo (+) / (-) e volumine cellulae (lyophil., steril.)
3X

Composition: 1 suppository contains: Medically active substance: 0.2 g Mucor


mucedo (+) / (-) volumine cellulae (lyophil., steril.) 3X trit. Other
constituents: hard fat, lactose.

According to experience, Neuro-vegetative syndrome, regulatory dysfunctions in the limbic system,


to be administered in anxiety, depression; respiratory diseases, sinusitis, tonsillitis, sino-
cases of: bronchitis; ostitis; lymphostasis; thyroidal disorders.

Characteristics: Mucedokehl contains Mucor mucedo as active ingredient and


is administered especially in disorders which are connected with the
neuro-vegetative system.

Application: Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally.


Children between the age of 4 and 6 years should not receive more than
half of the dosage for adults; children between the age of 6 and 12 years
should not receive more than 2/3 of the dosage for adults.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Mucedokehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Mucor mucedo).

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

92
Mucedokehl 4X
Capsules
for oral intake

Active ingredient: Mucor mucedo (+) / (-) e volumine cellulae (lyophil., steril.)
4X

Composition: 1 capsule contains: Medically active substance: 330 mg Mucor


mucedo (+) / (-) e volumine cellulae (lyophil., steril.) 4X trit.
Other constituents: lactose, hypromellosis (capsule shell).

According to experience, Neuro-vegetative syndrome, regulatory dysfunctions in the limbic system,


to be administered in anxiety, depression; respiratory diseases, sinusitis, tonsillitis, sino-
cases of: bronchitis; ostitis; lymphostasis; thyroidal disorders.

Characteristics: Mucedokehl contains Mucor mucedo as active ingredient and


is administered especially in disorders which are connected with the
neuro-vegetative system.

Application: Unless otherwise prescribed: 1-3 x daily 1 capsule.


Children between the age of 4 and 6 years should not receive more than
half of the dosage for adults; children between the age of 6 and 12 years
should not receive more than 2/3 of the dosage for adults.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Mucedokehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Mucor mucedo).

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

93
Mucedokehl 5X
Ampules
Liquid dilution for injection

Active ingredient: Mucor mucedo (+) / (-) e volumine cellulae (lyophil., steril.)
5X

Composition: 1 ampule of 1 ml contains:: Medically active substance: 10 ml Mucor


mucedo (+) / (-) e volumine cellulae (lyophil., steril.) 5X dil.
Other constituents: isotonic sodium chloride solution.

According to experience, Neuro-vegetative syndrome, regulatory dysfunctions in the limbic system,


to be administered in anxiety, depression; respiratory diseases, sinusitis, tonsillitis, sino-
cases of: bronchitis; ostitis; lymphostasis; thyroidal disorders.

Characteristics: Mucedokehl contains Mucor mucedo as active ingredient and


is administered especially in disorders which are connected with the
neuro-vegetative system.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3
x weekly.
Children between the age of 4 and 6 years should not receive more than
half of the dosage for adults; children between the age of 6 and 12 years
should not receive more than 2/3 of the dosage for adults.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Mucedokehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Mucor mucedo).

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

94
Mucedokehl 5X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Mucor mucedo (+) / (-) e volumine cellulae (lyophil., steril.)
5X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Mucor


mucedo (+) / (-) e volumine cellulae (lyophil., steril.) 5X dil.
Other constituents: purified water.

According to experience, Neuro-vegetative syndrome, regulatory dysfunctions in the limbic system,


to be administered in anxiety, depression; respiratory diseases, sinusitis, tonsillitis, sino-
cases of: bronchitis; ostitis; lymphostasis; thyroidal disorders.

Characteristics: Mucedokehl contains Mucor mucedo as active ingredient and


is administered especially in disorders which are connected with the
neuro-vegetative system.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Children between the age of 4 and 6 years should not receive more than
half of the dosage for adults; children between the age of 6 and 12 years
should not receive more than 2/3 of the dosage for adults.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Mucedokehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Mucor mucedo).

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

95
Mucokehl 3X
Ointment
for rubbing in

Active ingredient: Mucor racemosus e volumine cellulae (lyophil., steril.) 3X

Composition: 1 g ointment contains: Medically active substance: 0.1 g Mucor


racemosus e volumine cellulae (lyophil., steril.) 3X dil. Other
constituents: 0.38 g lanolin alcohol ointment, 0.10 g coconut oil fract.,
0.03 g glyceryl monostearate 40-55%, 0.23 g propylene glycol, 0.02
g magnesium sulphate x 7 H2O, 0.01 g lactic acid, 0.13 g water for
injection.

According to experience, Diseases of the veins and their disturbed circulation such as varicosis,
to be administered in thrombophlebitis, hemorrhoids; generally for inflammatory diseases;
cases of: swellings, contusions, distortions, ischialgia, chronic pain syndrome;
cicatricial keloids, chronic dermatitis, neurodermatitis; ovarian und tubal
cysts (locally on the lower abdomen); tentatively in cases of Dupuytrens
contracture and flexion contracture.

Characteristics: In Isopathy Mucokehl is administered for all disorders of the blood


and circulatory system and resulting diseases (congestion).

Application: Unless otherwise prescribed: Apply thinly on the affected area 1 to 3 x


daily.

Side effects: Because of specific organic components of Mucokehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Mucor racemosus).

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Additional advice: Mucor racemosus as an active ingredient is also contained in


Sankombi.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X, 10 single use
vials eye drops 5X (preservative-free).

96
Mucokehl 3X
Suppositories
for rectal application

Active ingredient: Mucor racemosus e volumine cellulae (lyophil., steril.) 3X

Composition: 1 suppository contains: Medically active substance: 0.2 g Mucor


racemosus e volumine cellulae (lyophil., steril.) 3X trit. Other
constituents: hard fat, lactose.

According to experience, Chronic, latent and acute infirmities of the vascular system, such as
to be administered in thromboses embolism, post-infarct processes, angina pectoris, circulatory
cases of: disorders and disturbed healing of wounds, such as smokers leg,
diabetic gangrene, neurodermatitis, venous diseases, such as
varicosity, hemorrhoids, fissure ani; glaucoma; inflammatory diseases
of the organs and the connective tissue in the small pelvis, such as
endometritis, prostatitis, colitis syndrome, diverticulitis, prostate
adenoma; precanceroses; lymphostasis; chronic pain syndrome.

Characteristics: In Isopathy Mucokehl is administered for all disorders of the blood


and circulatory system and resulting diseases (congestion).

Application: Unless otherwise prescribed: 1 x daily, insert 1 suppository.


Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Mucokehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Mucor racemosus).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Mucokehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

Additional advice: Mucor racemosus as an active ingredient is also contained in


Sankombi.

Duration of treatment: Dependent on the advice of the physician or health care professional.

97
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X, 10 single use
vials eye drops 5X (preservative-free).

98
Mucokehl 4X
Capsules
for oral intake

Active ingredient: Mucor racemosus e volumine cellulae (lyophil., steril.) 4X

Composition: 1 capsule contains: Medically active substance: 330 mg Mucor


racemosus e volumine cellulae (lyophil., steril.) 4X trit. Other
constituents: lactose, hypromellosis (capsule shell).

According to experience, Chronic, latent and acute infirmities of the vascular system, such as
to be administered in thromboses, embolism, post-infarct processes, angina pectoris, circu-
cases of: latory disorders and disturbed healing of wounds, such as smokers
leg, diabetic gangrene, neurodermatitis, venous diseases, such as
varicosity, hemorrhoids, fissure ani; glaucoma; inflammatory diseases
of the organs and the connective tissue in the small pelvis, such as
endometritis, prostatitis, colitis syndrome, diverticulitis, prostate
adenoma; precanceroses; lymphostasis; chronic pain syndrome.

Characteristics: In Isopathy Mucokehl is administered for all disorders of the blood


and circulatory system and resulting diseases (congestion).

Application: Unless otherwise prescribed: 1-3 x daily 1 capsule.


Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Mucokehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Mucor racemosus).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Mucokehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

Additional advice: Mucor racemosus as an active ingredient is also contained in


Sankombi.

Duration of treatment: Dependent on the advice of the physician or health care professional.

99
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X, 10 single use
vials eye drops 5X (preservative-free).

100
Mucokehl 5X
Ampules
Liquid dilution for injection

Active ingredient: Mucor racemosus e volumine cellulae (lyophil., steril.) 5X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Mucor


racemosus e volumine cellulae (lyophil., steril.) 5X aquous dil.
Other constituents: isotonic sodium chloride solution.

According to experience, Chronic, latent and acute infirmities of the vascular system, such as
to be administered in thromboses, embolism, post-infarct processes, angina pectoris, circu-
cases of: latory disorders and disturbed healing of wounds, such as smokers
leg, diabetic gangrene, neurodermatitis, venous diseases, such as
varicosity, hemorrhoids, fissure ani; glaucoma; inflammatory diseases
of the organs and the connective tissue in the small pelvis, such as
endometritis, prostatitis, colitis syndrome, diverticulitis, prostate
adenoma; precanceroses; lymphostasis; chronic pain syndrome.

Characteristics: In Isopathy Mucokehl is administered for all disorders of the blood


and circulatory system and resulting diseases (congestion).

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3
x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Mucokehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Mucor racemosus).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Mucokehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Additional advice: Mucor racemosus as an active ingredient is also contained in


Sankombi.

Duration of treatment: Dependent on the advice of the physician or health care professional.

101
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X, 10 single use
vials eye drops 5X (preservative-free).

102
Mucokehl 5X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Mucor racemosus e volumine cellulae (lyophil., steril.) 5X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Mucor


racemosus e volumine cellulae (lyophil., steril.) 5X dil. Other
constituents: purified water.

According to experience, Chronic, latent and acute infirmities of the vascular system, such as
to be administered in thromboses, embolism, post-infarct processes, angina pectoris, circu-
cases of: latory disorders and disturbed healing of wounds, such as smokers
leg, diabetic gangrene, neurodermatitis, venous diseases, such as
varicosity, hemorrhoids, fissure ani; glaucoma; inflammatory diseases
of the organs and the connective tissue in the small pelvis, such as
endometritis, prostatitis, colitis syndrome, diverticulitis, prostate
adenoma; precanceroses; lymphostasis; chronic pain syndrome.

Characteristics: In Isopathy Mucokehl is administered for all disorders of the blood


and circulatory system and resulting diseases (congestion).

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Mucokehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Mucor racemosus).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Mucokehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: After opening, contents must be used within two months.

Additional advice: Mucor racemosus as an active ingredient is also contained in


Sankombi.

103
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X , 10 single use
vials eye drops 5X (preservative-free).

104
Mucokehl 5X
Eye drops
Liquid dilution for the eyes

Active ingredient: Mucor racemosus e volumine cellulae (lyophil., steril.) 5X

Composition: 5 ml liquid dilution contains: Medically active substance: 4.999.95 mg


Mucor racemosus e volumine cellulae (lyophil., steril.) 5X dil.
Other constituents: isotonic sodium chloride solution, 0.05 mg
chlorohexidinediacetate.

According to experience, Glaucoma, cataract, conjunctivitis, dry eye syndrome.


to be administered in
cases of:

Characteristics: In Isopathy Mucokehl is administered for all disorders of the blood


and circulatory system and resulting diseases (congestion).

Application: Dosage depends on the indication: Conjunctivitis: Drip 1 drop


several times daily into the affected eye, and also treat the other eye, if
it is necessary. Dry Eye Syndrome: Drip 1 drop twice daily into both
eyes, preferably in the morning and in the evening. For other dosage
information, please see your physician or dispensing pharmacist, who
will be able to assist you.

Side effects: Because of specific organic components of Mucokehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: In cases of known hypersensitivity to Mucor racemosus, as a


precaution, this preparation should not be administered.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: To avoid contamination, do not touch tip of dropper to any surface. This
remedy should be used within one month of opening.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X, 10 single use
vials eye drops 5X (preservative-free).

105
Mucokehl 5X
Eye drops in single use vials (preservative-free)
Liquid dilution for the eyes

Active ingredient: Mucor racemosus e volumine cellulae (lyophil., steril.) 5X

Composition: 1 single use vial contains: Medically active substance per 0.017 fl oz / 0.5 ml
vial: 0.05 mg Mucor racemosus e volumine cellulae (lyophil.,
steril.) 5X dil. Other constituents: water, salt.

According to experience, Glaucoma, cataract, conjunctivitis, dry eye syndrome.


to be administered in
cases of:

Characteristics: In Isopathy Mucokehl is administered for all disorders of the blood


and circulatory system and resulting diseases (congestion).

Application: Dosage depends on the indication: Conjunctivitis: Drip 1 drop


several times daily into the affected eye, and also treat the other eye, if
it is necessary. Dry Eye Syndrome: Drip 1 drop twice daily into both
eyes, preferably in the morning and in the evening. For other dosage
information, please see your physician or dispensing pharmacist, who
will be able to assist you.

Side effects: Because of specific organic components of Mucokehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: In cases of known hypersensitivity to Mucor racemosus, as a


precaution, this preparation should not be administered.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: To avoid contamination, do not touch tip of vial to any surface. Do not
use if vial is broken or damaged. Use vials up before the expiry date or
before the expiration of 6 months after opening the bag and within 24
hours after opening the vial.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X, 10 single use
vials eye drops 5X (preservative-free).

106
Mucokehl 5X
Tablets
for oral intake

Active ingredient: Mucor racemosus e volumine cellulae (lyophil., steril.) 5X

Composition: 1 tablet contains: Medically active substance: 250 mg Mucor race


mosus e volumine cellulae (lyophil., steril.) 5X trit. Other
constituents: lactose, potato starch, magnesium stearate.

According to experience, Chronic, latent and acute infirmities of the vascular system, such as
to be administered in thromboses, embolism, post-infarct processes, angina pectoris, circu-
cases of: latory disorders and disturbed healing of wounds, such as smokers
leg, diabetic gangrene, neurodermatitis, venous diseases, such as
varicosity, hemorrhoids, fissure ani; glaucoma; inflammatory diseases
of the organs and the connective tissue in the small pelvis, such as
endometritis, prostatitis, colitis syndrome, diverticulitis, prostate
adenoma; precanceroses; lymphostasis; chronic pain syndrome.

Characteristics: In Isopathy Mucokehl is administered for all disorders of the blood


and circulatory system and resulting diseases (congestion).

Application: Unless otherwise prescribed: 1-3 x daily 1 tablet.


Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Mucokehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Mucor racemosus).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Mucokehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

Additional advice: Mucor racemosus as an active ingredient is also contained in


Sankombi.

Duration of treatment: Dependent on the advice of the physician or health care professional.

107
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X, 10 single use
vials eye drops 5X (preservative-free).

108
Mucokehl 6X
Ampules
Liquid dilution for injection

Active ingredient: Mucor racemosus e volumine cellulae (lyophil., steril.) 6X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Mucor


racemosus e volumine cellulae (lyophil., steril.) 6X aquous dil.
Other constituents: isotonic sodium chloride solution.

According to experience, Chronic, latent and acute infirmities of the vascular system, such as
to be administered in thromboses, embolism, post-infarct processes, angina pectoris, circu-
cases of: latory disorders and disturbed healing of wounds, such as smokers
leg, diabetic gangrene, neurodermatitis, venous diseases, such as
varicosity, hemorrhoids, fissure ani; glaucoma; inflammatory diseases
of the organs and the connective tissue in the small pelvis, such as
endometritis, prostatitis, colitis syndrome, diverticulitis, prostate
adenoma; precanceroses; lymphostasis; chronic pain syndrome.

Characteristics: In Isopathy Mucokehl is administered for all disorders of the blood


and circulatory system and resulting diseases (congestion).

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3
x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Mucokehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Mucor racemosus).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Mucokehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Additional advice: Mucor racemosus as an active ingredient is also contained in


Sankombi.

Duration of treatment: Dependent on the advice of the physician or health care professional.

109
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X, 10 single use
vials eye drops 5X (preservative-free).

110
Mucokehl 7X
Ampules
Liquid dilution for injection

Active ingredient: Mucor racemosus e volumine cellulae (lyophil., steril.) 7X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Mucor


racemosus e volumine cellulae (lyophil., steril.) 7X aquous dil.
Other constituents: isotonic sodium chloride solution.

According to experience, Chronic, latent and acute infirmities of the vascular system, such as
to be administered in thromboses, embolism, post-infarct processes, angina pectoris, circu-
cases of: latory disorders and disturbed healing of wounds, such as smokers
leg, diabetic gangrene, neurodermatitis, venous diseases, such as
varicosity, hemorrhoids, fissure ani; glaucoma; inflammatory diseases
of the organs and the connective tissue in the small pelvis, such as
endometritis, prostatitis, colitis syndrome, diverticulitis, prostate
adenoma; precanceroses; lymphostasis; chronic pain syndrome.

Characteristics: In Isopathy Mucokehl is administered for all disorders of the blood


and circulatory system and resulting diseases (congestion).

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3
x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Mucokehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Mucor racemosus).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Mucokehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Additional advice: Mucor racemosus as an active ingredient is also contained in


Sankombi.

Duration of treatment: Dependent on the advice of the physician or health care professional.

111
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X, 10 single use
vials eye drops 5X (preservative-free).

112
Mucokehl Atox 6X
Ampules
Liquid dilution for injection

Active ingredient: Mucor racemosus serum oryctolagi (steril.) 6X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml rabbit


serum 6X dil., derived from rabbits that were pre-treated with Mucor
racemosus 2X/3X dil. Other constituents: isotonic sodium chloride
solution.

According to experience, Elimination after application of Mucokehl.


to be administered in
cases of:

Characteristics: Mucokehl Atox 6X is a highly effective preparation for supporting


elimination of metabolic and decomposition products, especially after
application of Mucokehl. Every effective biological therapy leads to
an increase of degradation products and toxins which frequently fail to
be eliminated due to blockages and congestive conditions. Because
this could worsen a disease, elimination is the basic requirement for an
effective therapy.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously or intracutaneously, 1-3 x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Mucokehl Atox 6X,


theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,


especially rabbit protein.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: To be administered 1 day after Mucokehl at the earliest.


Drink plenty of fluids.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.

113
Mucokehl Atox 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Mucor racemosus serum oryctolagi (steril.) 6X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml rabbit


serum 6X dil., derived from rabbits that were pre-treated with Mucor
racemosus 2X/3X dil. Other constituents: purified water.

According to experience, Elimination after application of Mucokehl.


to be administered in
cases of:

Characteristics: Mucokehl Atox 6X is a highly effective preparation for supporting


elimination of metabolic and decomposition products, especially after
application of Mucokehl. Every effective biological therapy leads to
an increase of degradation products and toxins which frequently fail to
be eliminated due to blockages and congestive conditions. Because
this could worsen a disease, elimination is the basic requirement for an
effective therapy.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Mucokehl Atox 6X,


theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,


especially rabbit protein.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: After opening, contents must be used within two months.


To be administered 1 day after Mucokehl at the earliest.
Drink plenty of fluids.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.

114
Muscarsan 6X
Ampules
Liquid dilution for injection

Active ingredient: Amanita muscaria e thallo 6X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Amanita


muscaria e thallo 6X aquous dil. Other constituents: isotonic sodium
chloride solution.

According to experience, Detoxification in case of drug and medication abuse; cerebral ischaemic
to be administered in attack; nervous and cerebral hyperexcitability; spasms of muscles, organs
cases of: and blood vessels, migraine; nervous disorders of the intestine.

Characteristics: The Amanita muscaria fungus is known for its characteristic


appearance and toxicity. The occurring symptoms after the consumption
of dried fly agaric are similar to those which arise after drug abuse.
Amanita muscaria is applied for therapeutic purposes in homeopathy
whereby the range of application is relatively broad. Important areas of
application are cerebral and nervous overexcitement and exhaustion
conditions, headache with pupils or students, cerebral circulatory
disorders, vertigo, intoxicated and ecstatic conditions, muscular and
organic spasms, migraine and vascular spasms, nervous disorders
of the intestinal tract, gastralgia, meteorism, chronic fermentative
dyspepsia, damage from coffee and tabacco, alcoholism, drug and
tablet abuse.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously or intracutaneously 1-3x weekly.

Side effects: Because of specific organic components of Muscarsan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Amanita


muscaria.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X, 80 tablets 6X.

115
Muscarsan 6X
Drops
Liquid dilution for oral intake

Active ingredient: Amanita muscaria e thallo 6X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Amanita


muscaria e thallo 6X dil. Other constituents: purified water, ethanol.

According to experience, Detoxification in case of drug and medication abuse; cerebral ischaemic
to be administered in attack; nervous and cerebral hyperexcitability; spasms of muscles,
cases of: organs and blood vessels, migraine; nervous disorders of the intestine.

Characteristics: The Amanita muscaria fungus is known for its characteristic


appearance and toxicity. The occurring symptoms after the consumption
of dried fly agaric are similar to those which arise after drug abuse.
Amanita muscaria is applied for therapeutic purposes in homeopathy
whereby the range of application is relatively broad. Important areas of
application are cerebral and nervous overexcitement and exhaustion
conditions, headache with pupils or students, cerebral circulatory
disorders, vertigo, intoxicated and ecstatic conditions, muscular and
organic spasms, migraine and vascular spasms, nervous disorders
of the intestinal tract, gastralgia, meteorism, chronic fermentative
dyspepsia, damage from coffee and tabacco, alcoholism, drug and
tablet abuse.

Application: Unless otherwise prescribed:


For oral intake: 1 x daily 5-10 drops.

Side effects: Because of specific organic components of Muscarsan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Amanita


muscaria.
This product contains 50 % (v/v) alcohol (ethanol). Following the dosage
recommendations, 5 drops lead to an alcohol intake of 0.05 g. This may
present a health risk in cases of liver diseases, alcoholism, epilepsy,
brain damage, pregnancy, and in children. The action of other drugs
may be reduced or intensified.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

116
Advice: This product contains 50 % (v/v) alcohol (ethanol).

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X, 80 tablets 6X.

117
Muscarsan 6X
Tablets
for oral intake

Active ingredient: Amanita muscaria e thallo 6X

Composition: 1 tablet contains: Medically active substance: 250 mg Amanita mus


caria e thallo 6X trit. Other constituents: lactose, potato starch,
magnesium stearate.

According to experience, Detoxification in case of drug and medication abuse; cerebral ischaemic
to be administered in attack; nervous and cerebral hyperexcitability; spasms of muscles, organs
cases of: and blood vessels, migraine; nervous disorders of the intestine.

Characteristics: The Amanita muscaria fungus is known for its characteristic


appearance and toxicity. The occurring symptoms after the consumption
of dried fly agaric are similar to those which arise after drug abuse.
Amanita muscaria is applied for therapeutic purposes in homeopathy
whereby the range of application is relatively broad. Important areas of
application are cerebral and nervous overexcitement and exhaustion
conditions, headache with pupils or students, cerebral circulatory
disorders, vertigo, intoxicated and ecstatic conditions, muscular and
organic spasms, migraine and vascular spasms, nervous disorders
of the intestinal tract, gastralgia, meteorism, chronic fermentative
dyspepsia, damage from coffee and tabacco, alcoholism, drug and
tablet abuse.

Application: Unless otherwise prescribed: 1-3 x daily 1 tablet.

Side effects: Because of specific organic components of Muscarsan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Amanita


muscaria.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X, 80 tablets 6X.

118
Nigersan 3X
Suppositories
for rectal application

Active ingredient: Aspergillus niger e volumine cellulae (lyophil., steril.) 3X

Composition: 1 suppository contains: Medically active substance: 0.2 g Aspergillus


niger e volumine cellulae (lyophil., steril.) 3X trit. Other consti
tuents: hard fat, lactose.

According to experience, Diseases of the urogenital tract, such as myoma, cysts, prostate adenoma;
to be administered in degenerative or inflammatory conditions, such as Scheuermann disease,
cases of: Perthes disease and Bechterews disease; disorders of the respiratory
tract; lymphatism; goiter diseases; obesity; verrucae (warts).

Characteristics: Nigersan is produced from the mold fungus Aspergillus niger.


Nigersan is a specifically acting preparation for treatment of tuber
culinic constitution and resulting diseases.

Application: Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally.


Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Nigersan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Aspergillus niger).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Nigersan.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

Additional advice: Aspergillus niger as an active ingredient is also contained in


Sankombi.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.

119
Nigersan 4X
Capsules
for oral intake

Active ingredient: Aspergillus niger e volumine cellulae (lyophil., steril.) 4X

Composition: 1 capsule contains: Medically active substance: 330 mg Aspergillus


niger e volumine cellulae (lyophil., steril.) 4X trit. Other consti
tuents: lactose, hypromellosis (capsule shell).

According to experience, Diseases of the urogenital tract, such as myoma, cysts, prostate adenoma;
to be administered in degenerative or inflammatory conditions, such as Scheuermann disease,
cases of: Perthes disease and Bechterews disease; disorders of the respiratory
tract; lymphatism; goiter diseases; obesity; verrucae (warts).

Characteristics: Nigersan is produced from the mold fungus Aspergillus niger.


Nigersan is a specifically acting preparation for treatment of tuber
culinic constitution and resulting diseases.

Application: Unless otherwise prescribed: 1-3 x daily 1 capsule.


Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Nigersan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Aspergillus niger).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Nigersan.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

Additional advice: Aspergillus niger as an active ingredient is also contained in


Sankombi.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.

120
Nigersan 5X
Ampules
Liquid dilution for injection

Active ingredient: Aspergillus niger e volumine cellulae (lyophil., steril.) 5X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Aspergillus


niger e volumine cellulae (lyophil., steril.) 5X aquous dil. Other
constituents: isotonic sodium chloride solution.

According to experience, Diseases of the urogenital tract, such as myoma, cysts, prostate adenoma;
to be administered in degenerative or inflammatory conditions, such as Scheuermann disease,
cases of: Perthes disease and Bechterews disease; disorders of the respiratory
tract; lymphatism; goiter diseases; obesity; verrucae (warts).

Characteristics: Nigersan is produced from the mold fungus Aspergillus niger.


Nigersan is a specifically acting preparation for treatment of tuber
culinic constitution and resulting diseases.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3
x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Nigersan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Aspergillus niger).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Nigersan.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Additional advice: Aspergillus niger as an active ingredient is also contained in


Sankombi.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.

121
Nigersan 5X
Drops
Liquid dilution
for oral intake, rubbing in, inhalation

Active ingredient: Aspergillus niger e volumine cellulae (lyophil., steril.) 5X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Aspergillus niger e volumine cellulae (lyophil., steril.) 5X dil.
Other constituents: purified water.

According to experience, Diseases of the urogenital tract, such as myoma, cysts, prostate adenoma;
to be administered in degenerative or inflammatory conditions, such as Scheuermann disease,
cases of: Perthes disease and Bechterews disease; disorders of the respiratory
tract; lymphatism; goiter diseases; obesity; verrucae (warts).

Characteristics: Nigersan is produced from the mold fungus Aspergillus niger.


Nigersan is a specifically acting preparation for treatment of tuber
culinic constitution and resulting diseases.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops.
For rubbing in: 1 x daily 5-10 drops into the bend of the elbow. For
inhalation: 10-20 drops, inhaled deeply 2-3 x daily.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Nigersan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Aspergillus niger).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Nigersan.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: After opening, contents must be used within two months.

Additional advice: Aspergillus niger as an active ingredient is also contained in


Sankombi.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.

122
Nigersan 5X
Tablets
for oral intake

Active ingredient: Aspergillus niger e volumine cellulae (lyophil., steril.) 5X

Composition: 10 tablet contains: Medically active substance: 250 mg Aspergillus


niger e volumine cellulae (lyophil., steril.) 5X trit. Other consti
tuents: lactose, potato starch, magnesium stearate.

According to experience, Diseases of the urogenital tract, such as myoma, cysts, prostate adenoma;
to be administered in degenerative or inflammatory conditions, such as Scheuermann disease,
cases of: Perthes disease and Bechterews disease; disorders of the respiratory
tract; lymphatism; goiter diseases; obesity; verrucae (warts).

Characteristics: Nigersan is produced from the mold fungus Aspergillus niger.


Nigersan is a specifically acting preparation for treatment of tuber
culinic constitution and resulting diseases.

Application: Unless otherwise prescribed: 1-3 x daily 1 tablet.


Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Nigersan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Aspergillus niger).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Nigersan.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

Additional advice: Aspergillus niger as an active ingredient is also contained in


Sankombi.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.

123
Nigersan 6X
Ampules
Liquid dilution for injection

Active ingredient: Aspergillus niger e volumine cellulae (lyophil., steril.) 6X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Aspergillus


niger e volumine cellulae (lyophil., steril.) 6X aquous dil. Other
constituents: isotonic sodium chloride solution.

According to experience, Diseases of the urogenital tract, such as myoma, cysts, prostate adenoma;
to be administered in degenerative or inflammatory conditions, such as Scheuermann disease,
cases of: Perthes disease and Bechterews disease; disorders of the respiratory
tract; lymphatism; goiter diseases; obesity; verrucae (warts).

Characteristics: Nigersan is produced from the mold fungus Aspergillus niger.


Nigersan is a specifically acting preparation for treatment of tuber
culinic constitution and resulting diseases.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3
x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Nigersan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Aspergillus niger).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Nigersan.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: None.

Additional advice: Aspergillus niger as an active ingredient is also contained in


Sankombi.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.

124
Nigersan 7X
Ampules
Liquid dilution for injection

Active ingredient: Aspergillus niger e volumine cellulae (lyophil., steril.) 7X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Aspergillus


niger e volumine cellulae (lyophil., steril.) 7X aquous dil. Other
constituents: isotonic sodium chloride solution.

According to experience, Diseases of the urogenital tract, such as myoma, cysts, prostate adenoma;
to be administered in degenerative or inflammatory conditions, such as Scheuermann disease,
cases of: Perthes disease and Bechterews disease; disorders of the respiratory
tract; lymphatism; goiter diseases; obesity; verrucae (warts).

Characteristics: Nigersan is produced from the mold fungus Aspergillus niger.


Nigersan is a specifically acting preparation for treatment of tuber
culinic constitution and resulting diseases.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3
x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Nigersan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Aspergillus niger).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Nigersan.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: None.

Additional advice: Aspergillus niger as an active ingredient is also contained in


Sankombi.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X.

125
Nigersan Atox 6X
Ampules
Liquid dilution for injection

Active ingredient: Aspergillus niger serum oryctolagi (steril.) 6X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml rabbit serum


6X dil., derived from rabbits that were pre-treated with Aspergillus
niger 2X/3X dil. Other constituents: isotonic sodium chloride
solution.

According to experience, Elimination after application of Nigersan.


to be administered in
cases of:

Characteristics: Nigersan Atox 6X is a highly effective preparation for supporting


elimination of metabolic and decomposition products, especially after
application of Nigersan. Every effective biological therapy leads to
an increase of degradation products and toxins which frequently fail to
be eliminated due to blockages and congestive conditions. Because
this could worsen a disease, elimination is the basic requirement for an
effective therapy.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously or intracutaneously, 1-3 x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Nigersan Atox 6X,


theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,


especially rabbit protein.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: To be administered 1 day after Nigersan at the earliest.


Drink plenty of fluids.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.

126
Nigersan Atox 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Aspergillus niger serum oryctolagi (steril.) 6X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


rabbit serum 6X dil., derived from rabbits that were pre-treated with
Aspergillus niger 2X/3X dil. Other constituents: purified water.

According to experience, Elimination after application of Nigersan.


to be administered in
cases of:

Characteristics: Nigersan Atox 6X is a highly effective preparation for supporting


elimination of metabolic and decomposition products, especially after
application of Nigersan. Every effective biological therapy leads to
an increase of degradation products and toxins which frequently fail to
be eliminated due to blockages and congestive conditions. Because
this could worsen a disease, elimination is the basic requirement for an
effective therapy.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Nigersan Atox 6X,


theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,


especially rabbit protein.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: After opening, contents must be used within two months.


To be administered 1 day after Nigersan at the earliest.
Drink plenty of fluids.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.

127
Notakehl 3X
Ointment
for rubbing in

Active ingredient: Penicillium chrysogenum e volumine cellulae (lyophil., steril.) 3X

Composition: 1 g ointment contains: Medically active substance: 0.1 g Penicillium


chrysogenum e volumine cellulae (lyophil., steril.) 3X dil. Other
constituents: 0.38 g lanolin alcohol ointment, 0.10 g coconut oil fract.,
0.03 g glyceryl monostearate 40-55%, 0.23 g propylene glycol, 0.02 g
magnesium sulphate x 7 H2O, 0.01 g lactic acid, 0.13 g water for injection.

According to experience, Bacterial disorders, e.g. tonsillitis, laryngitis, otitis; diseases of the
to be administered in urogenital system, such as cystitis, prostatitis, endometriosis; respiratory
cases of: diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis; neuritis,
neuralgia, cervical spine and lumbar spine syndrome; suppurations,
acne, after tooth extractions.

Characteristics: Notakehl is produced from the mold fungus Penicillium chryso


genum and is administered in cases of bacterial diseases. Notakehl
is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damages, destruction
of intestinal flora and the formation of Penicillin resistant strains.

Application: Unless otherwise prescribed: Apply thinly on the affected area 1 to 3 x


daily.

Side effects: Because of specific organic components of Notakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Penicillium chrysogenum).

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Additional advice: Penicillium chrysogenum as an active ingredient is also contained


in Nota-Quent.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X.

128
Notakehl 3X
Suppositories
for rectal application

Active ingredient: Penicillium chrysogenum e volumine cellulae (lyophil., steril.) 3X

Composition: 1 suppository contains: Medically active substance: 0.2 g Penicillium


chrysogenum e volumine cellulae (lyophil., steril.) 3X trit. Other
constituents: hard fat, lactose.

According to experience, Bacterial disorders, e.g. tonsillitis, laryngitis, otitis; diseases of the
to be administered in urogenital system, such as cystitis, prostatitis, endometriosis; respiratory
cases of: diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis; neuritis,
neuralgia, cervical spine and lumbar spine syndrome; suppurations,
acne, after tooth extractions.

Characteristics: Notakehl is produced from the mold fungus Penicillium chryso


genum and is administered in cases of bacterial diseases. Notakehl
is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damages, destruction
of intestinal flora and the formation of Penicillin resistant strains.

Application: Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally.


Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Notakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Penicillium chrysogenum).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Notakehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

Additional advice: Penicillium chrysogenum as an active ingredient is also contained


in Nota-Quent.

129
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X.

130
Notakehl 4X
Capsules
for oral intake

Active ingredient: Penicillium chrysogenum e volumine cellulae (lyophil., steril.) 4X

Composition: 1 capsule contains: Medically active substance: 330 mg Penicillium


chrysogenum e volumine cellulae (lyophil., steril.) 4X trit. Other
constituents: lactose, hypromellosis (capsule shell).

According to experience, Bacterial disorders, e.g. tonsillitis, laryngitis, otitis; diseases of the
to be administered in urogenital system, such as cystitis, prostatitis, endometriosis; respiratory
cases of: diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis; neuritis,
neuralgia, cervical spine and lumbar spine syndrome; suppurations,
acne, after tooth extractions.

Characteristics: Notakehl is produced from the mold fungus Penicillium chryso


genum and is administered in cases of bacterial diseases. Notakehl
is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damages, destruction
of intestinal flora and the formation of Penicillin resistant strains.

Application: Unless otherwise prescribed: 1-3 x daily 1 capsule.


Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Notakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Penicillium chrysogenum).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Notakehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

Additional advice: Penicillium chrysogenum as an active ingredient is also contained


in Nota-Quent.

Duration of treatment: Dependent on the advice of the physician or health care professional.

131
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X.

132
Notakehl 5X
Ampules
Liquid dilution for injection

Active ingredient: Penicillium chrysogenum e volumine cellulae (lyophil., steril.) 5X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Penicillium


chrysogenum e volumine cellulae (lyophil., steril.) 5X aquous
dil. Other constituents: isotonic sodium chloride solution.

According to experience, Bacterial disorders, e.g. tonsillitis, laryngitis, otitis; diseases of the
to be administered in urogenital system, such as cystitis, prostatitis, endometriosis; respiratory
cases of: diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis; neuritis,
neuralgia, cervical spine and lumbar spine syndrome; suppurations,
acne, after tooth extractions.

Characteristics: Notakehl is produced from the mold fungus Penicillium chryso


genum and is administered in cases of bacterial diseases. Notakehl
is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damages, destruction
of intestinal flora and the formation of Penicillin resistant strains.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3 x
weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Notakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Penicillium chrysogenum).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Notakehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Additional advice: Penicillium chrysogenum as an active ingredient is also contained


in Nota-Quent.

Duration of treatment: Dependent on the advice of the physician or health care professional.

133
How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X.

134
Notakehl 5X
Drops
Liquid dilution
for oral intake, rubbing in, inhalation

Active ingredient: Penicillium chrysogenum e volumine cellulae (lyophil., steril.) 5X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Penicillium chrysogenum e volumine cellulae (lyophil., steril.)
5X dil. Other constituents: purified water.

According to experience, Bacterial disorders, e.g. tonsillitis, laryngitis, otitis; diseases of the
to be administered in urogenital system, such as cystitis, prostatitis, endometriosis; respiratory
cases of: diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis; neuritis,
neuralgia, cervical spine and lumbar spine syndrome; suppurations,
acne, after tooth extractions.

Characteristics: Notakehl is produced from the mold fungus Penicillium chrys


ogenum and is administered in cases of bacterial diseases. Notakehl
is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damages, destruction
of intestinal flora and the formation of Penicillin resistant strains.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops.
For rubbing in: 1 x daily 5-10 drops into the bend of the elbow. For
inhalation: 10-20 drops, inhaled deeply 2-3 x daily.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Notakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Penicillium chrysogenum).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Notakehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: After opening, contents must be used within two months.

Additional advice: Penicillium chrysogenum as an active ingredient is also contained


in Nota-Quent.

135
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X.

136
Notakehl 5X
Tablets
for oral intake

Active ingredient: Penicillium chrysogenum e volumine cellulae (lyophil., steril.) 5X

Composition: 1 tablet contains: Medically active substance: 250 mg Penicillium


chrysogenum e volumine cellulae (lyophil., steril.) 5X trit. Other
constituents: lactose, potato starch, magnesium stearate.

According to experience, Bacterial disorders, e.g. tonsillitis, laryngitis, otitis; diseases of the
to be administered in urogenital system, such as cystitis, prostatitis, endometriosis; respiratory
cases of: diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis; neuritis,
neuralgia, cervical spine and lumbar spine syndrome; suppurations,
acne, after tooth extractions.

Characteristics: Notakehl is produced from the mold fungus Penicillium chryso


genum and is administered in cases of bacterial diseases. Notakehl
is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damages, destruction
of intestinal flora and the formation of Penicillin resistant strains.

Application: Unless otherwise prescribed: 1-3 x daily 1 tablet.


Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Notakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Penicillium chrysogenum).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Notakehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

Additional advice: Penicillium chrysogenum as an active ingredient is also contained


in Nota-Quent.

137
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X.

138
Notakehl 6X
Ampules
Liquid dilution for injection

Active ingredient: Penicillium chrysogenum e volumine cellulae (lyophil., steril.) 6X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Penicillium


chrysogenum e volumine cellulae (lyophil., steril.) 6X aquous
dil. Other constituents: isotonic sodium chloride solution.

According to experience, Bacterial disorders, e.g. tonsillitis, laryngitis, otitis; diseases of the
to be administered in urogenital system, such as cystitis, prostatitis endometriosis; respiratory
cases of: diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis; neuritis,
neuralgia, cervical spine and lumbar spine syndrome; suppurations,
acne, after tooth extractions.

Characteristics: Notakehl is produced from the mold fungus Penicillium chryso


genum and is administered in cases of bacterial diseases. Notakehl
is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damages, destruction
of intestinal flora and the formation of Penicillin resistant strains.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3 x
weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Notakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Penicillium chrysogenum).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Notakehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: None.

Additional advice: Penicillium chrysogenum as an active ingredient is also contained


in Nota-Quent.

139
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X.

140
Notakehl 7X
Ampules
Liquid dilution for injection

Active ingredient: Penicillium chrysogenum e volumine cellulae (lyophil., steril.) 7X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Penicillium


chrysogenum e volumine cellulae (lyophil., steril.) 7X aquous
dilut. Other constituents: isotonic sodium chloride solution.

According to experience, Bacterial disorders, e.g. tonsillitis, laryngitis, otitis; diseases of the
to be administered in urogenital system, such as cystitis, prostatitis endometriosis; respiratory
cases of: diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis; neuritis,
neuralgia, cervical spine and lumbar spine syndrome; suppurations,
acne, after tooth extractions.

Characteristics: Notakehl is produced from the mold fungus Penicillium chryso


genum and is administered in cases of bacterial diseases. Notakehl
is not an antibiotic and does not produce antibiotic substances.
Therefore, there are no side effects like those which may occur during
treatment with antibiotics, such as allergies, liver damages, destruction
of intestinal flora and the formation of Penicillin resistant strains.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3 x
weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Notakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Penicillium chrysogenum).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Notakehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: None.

Additional advice: Penicillium chrysogenum as an active ingredient is also contained


in Nota-Quent.

141
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20
tablets 5X, 30 g tube of ointment 3X.

142
Nota-Quent 5X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredients: Penicillium chrysogenum e volumine cellulae (lyophil., steril.)


5X, Penicillium glabrum e volumine cellulae (lyophil., steril.) 5X

Composition: 10 ml liquid dilution contain: Medically active substance: 5 ml


Penicillium chrysogenum e volumine cellulae (lyophil., steril.)
5X dil., 5 ml Penicillium glabrum e volumine cellulae (lyophil.,
steril.) 5X dil. Other constituents: purified water.

According to experience, All acute and latent diseases caused by mixed bacterial and viral in-
to be administered in fections, such as tonsillitis, laryngitis, bronchitis, sinusitis, otitis, in-
cases of: fluenzal infections, asthma-bronchitis, bronchitis, sino-bronchitis; neuritis,
neuralgia; diseases of the urogenital system, such as cystitis, prostatitis,
endometriosis.

Characteristics: Nota-Quent is a combination of two specific preparations: Penicillium


chrysogenum and Penicillium glabrum. It is not an antibiotic and
does not produce antibiotic substances. Therefore, there are no side
effects like those which may occur during treatment with antibiotics,
such as allergies, liver damages, destruction of intestinal flora and the
formation of Penicillin resistant strains.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.

Side effects: Because of specific organic components of Nota-Quent, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Penicillium chrysogenum and Penicillium glabrum).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Nota-Quent.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage form is available: 10 ml dropper bottle 5X.

143
Okoubasan 2X
Drops
Liquid dilution
for oral intake

Active ingredient: Okoubaka aubrevillei 2X

Composition: 1 ml liquid dilution contains: Medically active substance: 1 ml Okoubaka


aubrevillei 2X dil. Other constituents: purified water, ethanol.

According to experience, Acute diarrhea, especially after food poisoning, infections of the gastro-
to be administered in intestinal tract, food intolerances, prophylactically in cases of change of
cases of nutrition and climate; during a regulation therapy for elimination of
metabolic waste products.

Characteristics: Okoubasan is produced from the dried bark of Okoubaka


aubrevillei, a tree which is mainly found in West Africa. In popular
medicine, the pulverized bark is internally administered as a detoxicant.
This old natives remedy was used by the chieftans food tasters in
order to protect them from poisoning. Today, Okoubaka aubrevillei
is also used for treatment of food poisoning and for healing infectious
diseases of the gastrointestinal tract.

Application: Unless otherwise prescribed:


For oral intake: in case of acute conditions 5 drops every half to full
hour. In case of chronic conditions 5 drops, 1-3 x times daily.

Side effects: Because of the specific organic components of Okoubasan,


theoretically, hypersensitivity may occur. In this case, discontinue use
and treat symptomatically.

Contraindications: This product contains 70 % (v/v) alcohol (ethanol). This may present
a health risk in cases of liver diseases, alcoholism, epilepsy, brain
damage, pregnancy, and in children. The action of other drugs may be
reduced or intensified.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains 70 % (v/v) alcohol (ethanol).

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 2X, 80
tablets 2X.

144
Okoubasan 2X
Tablets
for oral intake

Active ingredient: Okoubaka aubrevillei 2X

Composition: 1 tablet contains: Medically active substance: 250 mg Okoubaka


aubrevillei 2X trit. Other constituents: lactose, potato starch,
magnesium stearate.

Indication: Acute diarrhea, especially after food poisoning, infections of the gastro
intestinal tract, food intolerances, prophylactically in cases of change
of nutrition and climate; during a regulation therapy for elimination of
metabolic waste products.

Characteristics: Okoubasan is produced from the dried bark of Okoubaka


aubrevillei, a tree which is mainly found in West Africa. In popular
medicine, the pulverized bark is internally administered as a detoxicant.
This old natives remedy was used by the chieftans food tasters in
order to protect them from poisoning. Today, Okoubaka aubrevillei
is also used for treatment of food poisoning and for healing infectious
diseases of the gastrointestinal tract.

Application: Unless otherwise prescribed:


For oral intake: in case of acute conditions 1 tablet every half to full
hour up to a maximum of 12 times daily. In case of chronic conditions 2
tablets daily.

Side effects: Because of the specific organic components of Okoubasan,


theoretically, hypersensitivity may occur. In this case, discontinue use
and treat symptomatically.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 2X, 80
tablets 2X.

145
Pefrakehl 3X
Ointment
for rubbing in

Active ingredient: Candida parapsilosis e volumine cellulae (lyophil., steril.) 3X

Composition: 1 g ointment contains: Medically active substance: 0.1 g Candida


parapsilosis e volumine cellulae (lyophil., steril.) 3X dil. Other
constituents: 0.38 g lanolin alcohol ointment, 0.10 g coconut oil fract.,
0.03 g glyceryl monostearate 40-55%, 0.23 g propylene glycol, 0.02
g magnesium sulphate x 7 H2O, 0.01 g lactic acid, 0.13 g water for
injection.

According to experience, Disorders of the respiratory tract; intestinal mycoses, secondary


to be administered in mycotic diseases of the skin and the mucous membranes; all bacterial
cases of: and viral diseases, such as rhagades, aphthae, pemphigus vulgaris,
lymphadenitis, cystitis, otitis externa, acne, dental granuloma.

Characteristics: Pefrakehl is gained from mold fungus Candida parapsilosis and is


administered in cases of mycoses of the gastrointestinal tract, the skin
and the mucosa.

Application: Unless otherwise prescribed: Apply thinly on the affected area 1 to 3 x


daily.

Side effects: Because of specific organic components of Pefrakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Candida parapsilosis).

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: None.

Additional Advice: Candida parapsilosis as an active ingredient is also contained in


Exmykehl.

146
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 6X, 10 suppositories 3X, 20 capsules 4X, 30 g tube
of ointment 3X.

147
Pefrakehl 3X
Suppositories
for rectal application

Active ingredient: Candida parapsilosis e volumine cellulae (lyophil., steril.) 3X

Composition: 1 suppository contains: Medically active substance: 0.2 g Candida


parapsilosis e volumine cellulae (lyophil., steril.) 3X trit. Other
constituents: hard fat, lactose.

According to experience, Disorders of the respiratory tract; intestinal mycoses, secondary


to be administered in mycotic diseases of the skin and the mucous membranes; all
cases of: bacterial and viral diseases, such as rhagades, aphthae, pemphigus
vulgaris, lymphadenitis, cystitis, otitis externa, acne, dental granuloma.

Characteristics: Pefrakehl is gained from mold fungus Candida parapsilosis and is


administered in cases of mycoses of the gastrointestinal tract, the skin
and the mucosa.

Application: Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally.


Treatment of more than 8 weeks depends on the advice of the
physician or health care professional.

Side effects: Because of specific organic components of Pefrakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Candida parapsilosis).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Pefrakehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

Additional advice: Candida parapsilosis as an active ingredient is also contained in


Exmykehl.

148
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 6X, 10 suppositories 3X, 20 capsules 4X, 30 g tube
of ointment 3X.

149
Pefrakehl 4X
Capsules
for oral intake

Active ingredient: Candida parapsilosis e volumine cellulae (lyophil., steril.) 4X

Composition: 1 capsule contains: Medically active substance: 330 mg Candida


parapsilosis e volumine cellulae (lyophil., steril.) 4X trit.
Other constituents: lactose, hypromellosis (capsule shell).

According to experience, Disorders of the respiratory tract; intestinal mycoses, secondary


to be administered in mycotic diseases of the skin and the mucous membranes; all bac-
cases of: terial and viral diseases, such as rhagades aphthae, pemphigus
vulgaris, lymphadenitis, cystitis, otitis externa, acne, dental granuloma.

Characteristics: Pefrakehl is gained from mold fungus Candida parapsilosis and is


administered in cases of mycoses of the gastrointestinal tract, the skin
and the mucosa.

Application: Unless otherwise prescribed: 1-3 x daily 1 capsule.


Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Pefrakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Candida parapsilosis).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Pefrakehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

Additional advice: Candida parapsilosis as an active ingredient is also contained in


Exmykehl.

150
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 6X, 10 suppositories 3X, 20 capsules 4X, 30 g tube
of ointment 3X.

151
Pefrakehl 5X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Candida parapsilosis e volumine cellulae (lyophil., steril.) 5X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Candida


parapsilosis e volumine cellulae (lyophil., steril.) 5X dil. Other
constituents: purified water.

According to experience, Disorders of the respiratory tract; intestinal mycoses, secondary


to be administered in mycotic diseases of the skin and the mucous membranes; all bacterial
cases of: and viral diseases, such as rhagades, aphthae, pemphigus vulgaris,
lymphadenitis, cystitis, otitis externa, acne, dental granuloma.

Characteristics: Pefrakehl is gained from mold fungus Candida parapsilosis and is


administered in cases of mycoses of the gastrointestinal tract, the skin
and the mucosa.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Pefrakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Candida parapsilosis).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Pefrakehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: After opening, contents must be used within two months.

152
Additional advice: Candida parapsilosis as an active ingredient is also contained in
Exmykehl.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 6X, 10 suppositories 3X, 20 capsules 4X, 30 g tube
of ointment 3X.

153
Pefrakehl 6X
Ampules
Liquid dilution for injection

Active ingredient: Candida parapsilosis e volumine cellulae (lyophil., steril.) 6X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Candida


parapsilosis e volumine cellulae (lyophil., steril.) 6X aquous dil.
Other constituents: isotonic sodium chloride solution.

According to experience, Disorders of the respiratory tract; intestinal mycoses, secondary mycotic
to be administered in diseases of the skin and the mucous membranes; all bacterial and
cases of: viral diseases, such as rhagades, aphthae, pemphigus vulgaris,
lymphadenitis, cystitis, otitis externa, acne, dental granuloma.

Characteristics: Pefrakehl is gained from mold fungus Candida parapsilosis and is


administered in cases of mycoses of the gastrointestinal tract, the skin
and the mucosa.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3
x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Pefrakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Candida parapsilosis).

Adverse reactions: None known.

Interactions
with other remedies: Immunosuppressive drugs can influence the effectivity of Pefrakehl.
An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: None.

154
Additional Advice: Candida parapsilosis as an active ingredient is also contained in
Exmykehl.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 6X, 10 suppositories 3X, 20 capsules 4X, 30 g tube
of ointment 3X.

155
Pinikehl 4X
Capsules
for oral intake

Active ingredient: Fomitopsis pinicola e volumine cellulae (lyophil., steril.) 4X

Composition: 1 capsule contains: Medically active substance: 330 mg Fomitopsis


pinicola e volumine cellulae 4X trit. Other constituents: lactose
hypromellosis (capsule shell).

According to experience, Diseases of the liver and spleen, intermittent fever.


administered in
cases of:

Characteristics: Pinikehl is produced from Fomitopsis pinicola and is preferably


administered in weakness and disorders of liver and spleen.

Application: Unless otherwise prescribed: 1-3 x daily 1 capsule.


Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Pinikehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Fomitopsis


pinicola.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Pinikehl. An


with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

156
Pinikehl 4X
Suppositories
for rectal application

Active ingredient: Fomitopsis pinicola e volumine cellulae (lyophil., steril.) 4X

Composition: 1 suppository contains: Medically active substance: 0.2 g Fomitopsis


pinicola e volumine cellulae (lyophil., steril.) 4X trit. Other
constituents: hard fat, lactose.

According to experience, Diseases of the liver and spleen, intermittent fever.


administered in
cases of:

Characteristics: Pinikehl is produced from Fomitopsis pinicola and is preferably


administered in weakness and disorders of liver and spleen.

Application: Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally.


Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Pinikehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Fomitopsis


pinicola.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Pinikehl. An


with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

157
Pinikehl 5X
Ampules
Liquid dilution for injection

Active ingredient: Fomitopsis pinicola e volumine cellulae (lyophil., steril.) 5X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Fomitopsis


pinicola e volumine cellulae 5X aquous dil. Other constituents:
isotonic sodium chloride

According to experience, Diseases of the liver and spleen, intermittent fever.


administered in
cases of:

Characteristics: Pinikehl is produced from Fomitopsis pinicola and is preferably


administered in weakness and disorders of liver and spleen.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3x
weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Pinikehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Fomitopsis


pinicola.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Pinikehl. An


with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

158
Pinikehl 5X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Fomitopsis pinicola e volumine cellulae (lyophil., steril.) 5X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Fomitopsis pinicola e volumine cellulae (lyophil., steril.) 5X
dil. Other constituents: purified water.

According to experience, Diseases of the liver and spleen, intermittent fever.


administered in
cases of:

Characteristics: Pinikehl is produced from Fomitopsis pinicola and is preferably


administered in weakness and disorders of liver and spleen.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Pinikehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Fomitopsis


pinicola.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Pinikehl. An


with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

159
Pleo Chelate
Drops
Liquid dilution
for oral intake

Active ingredients: Sodium edetate 2X, hydrogen peroxide 2X, magnesium


sulphate 2X, potassium chloride 2X, sodium chloride 2X

Composition: 100 g solution contains: Medically active substances: 8 g sodium


edetate 2X, 8 g hydrogen peroxide 2X, 4 g magnesium sulphate
2X, 4 g potassium chloride 2X, 1.6 g Sodium chloride 2X. Other
constituents: purified water, ethanol.

According to experience, Reduction of high burden with heavy metals (e.g. lead in the air, mercury
to be administered in in tooth fillings, high levels of metals in drinking water, etc.).
cases of:

Characteristics: Pleo Chelate is able to stimulate the bodys capacity of chelating and
eliminating ionic metals such as mercury, lead and cadmium, thereby
reducing the production of harmful free radicals. Experience regarding
the use of the ingredients show that essential minerals such as calcium,
magnesium, potassium, sodium and selenium are not affected and
copper and zinc stay within physiological limits.

Application: Unless otherwise prescribed: Adults: Start with 5-30 drops daily
according to individual sensitivity and increase to 3x 10 in case of low
heavy metal burden, 3x 20 in case of medium heavy metal burden, 3x
30 in case of high heavy metal burden.
Children (5-10 years): 5-10 drops 3x daily.
The drops should be given into a glass of water with low mineral
contents.
Test of individual sensitivity towards Pleo Chelate: Rub in 5-10 drops
into the bend of the elbow. In case of skin reddening after 10 minutes,
start with lowest dosage and increase slowly.

Side effects: Gastrointestinal disturbances. slight myalgia, pruritus, xerostomia


or sensation of dizziness are possible during a high Pleo Chelate
administration.

Contraindications: Do not administer in cases of known hypersensitivity against sodium


edentate.
Do not administer during pregnancy.

Adverse reactions: None known.

160
Interactions Possible interference with chemotherapeutics, therefore, Pleo Chelate
with other remedies: should not be administered during chemotherapy.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: Sufficient fluid intake supports elimination of heavy metals, which are
bound by Pleo Chelate. Pleo Chelate helps the body to cope
better with environmental i.e. ionic heavy metals.
This product contains 3,5 % (v/v) alcohol (ethanol). Due to the alcohol
content, professional medical advice should be sought prior to
recommending this product to patients with alcohol or liver problems.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage form is available: 100 ml dropper bottle.

161
Polysan A 9X
Drops
Liquid dilution
for diagnosis, rubbing in

Active ingredient: Spengler colloid A 9X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Spengler colloid A 9X according to Dr. Carl Spengler with antigens
of Mycobacterium tuberculosis typus bovinus, Mycobacterium tuber-
culosis typus brevis as well as with the respective antitoxins from the
blood of highly immunized rabbits.

According to experience, Complaints due to aging, metabolic disorders, arteriosclerosis, hypertension,


to be administered in cardiac affections, nervous disorders; paradontosis; prostatic diseases,
cases of: joint and muscle stiffness; constipation.

Characteristics: The Polysans can be used therapeutically and also diagnostically.


In chronic diseases such as tuberculosis, rheumatism, cancer, etc.,
Carl Spengler, M.D., isolated gram-positive and gram-negative granula
from erythrocytes which he described as blood parasites. According
to Spengler, the gram-positive malignant granula disturb the binding
of oxygen to hemoglobin by their fermentation, thus endangering the
formation of defensive substances. It was his conviction that erythrocytes
infested with granula are the carriers of both inherited and endogenic
toxins. These specific inherited allergies are transferred from the mother
blood onto the child and may burden the descendants over several
generations. After cultivating the granula in special culture-media, Dr.
Spengler produced a vaccine which, in its homeopathically potentized
form, was suitable as a therapeutic agent for chronic infections and for
active immunization. When antibodies are present in human blood due
to a former disease, they react with the respective Spengler-colloid in
the sense of an antigen-antibody-reaction. This reaction is used in the
diagnostic blood test (developed by Schwarz). By using the Polysans
the body is stimulated to an intensified specific immune defense. It must
be noted that local complaints do not necessarily indicate chronic foci.
However, these must in each case be therapeutically treated, because
they are permanent disturbance fields and, as such, they block the
endogenic regulation of the organism.

Application: Unless otherwise prescribed: For rubbing in: apply 5-10 drops into the
bend of the elbow and rub in three times daily.
For diagnosis: A drop of the blood to be tested is mixed with a drop of the
Polysan antigens specified for the particular testing. Macroscopically
and microscopically visible agglutination occurs in the case of antigen-
antibody reaction. At the same time, the degree of agglutination is an
indicator of the level of antibody titer.

162
Side effects: None known. Because of specific organic components of Polysan A,
theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage form is available: 10 ml dropper bottle 9X.

163
Polysan D 9X
Drops
Liquid dilution
for diagnosis, rubbing in

Active ingredient: Spengler colloid D 9X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Spengler colloid D 9X according to Dr. Carl Spengler with antigens
from Streptococcus lacticus, pyogenes, hemolyticus, viridans,
Staphylococcus albus, pharyngis, aureus, Diplococcus lanceolatus,
Mycobacterium tuberculosis typus bovinus, as well as with the
respective antitoxins from the blood of highly immunized rabbits.

According to experience, Focal infections (in alternation with Polysan Dx); minor external skin
to be administered in infections.
cases of:

Characteristics: The Polysans can be used therapeutically and also diagnostically.


In chronic diseases such as tuberculosis, rheumatism, cancer, etc.,
Carl Spengler, M.D., isolated gram-positive and gram-negative granula
from erythrocytes which he described as blood parasites. According
to Spengler, the gram-positive malignant granula disturb the binding
of oxygen to hemoglobin by their fermentation, thus endangering the
formation of defensive substances. It was his conviction that erythrocytes
infested with granula are the carriers of both inherited and endogenic
toxins. These specific inherited allergies are transferred from the mother
blood onto the child and may burden the descendants over several
generations. After cultivating the granula in special culture-media, Dr.
Spengler produced a vaccine which, in its homeopathically potentized
form, was suitable as a therapeutic agent for chronic infections and for
active immunization. When antibodies are present in human blood due
to a former disease, they react with the respective Spengler-colloid in
the sense of an antigen-antibody-reaction. This reaction is used in the
diagnostic blood test (developed by Schwarz). By using the Polysans
the body is stimulated to an intensified specific immune defense. It must
be noted that local complaints do not necessarily indicate chronic foci.
However, these must in each case be therapeutically treated, because
they are permanent disturbance fields and, as such, they block the
endogenic regulation of the organism.

Application: Unless otherwise prescribed: For rubbing in: apply 5-10 drops into the
bend of the elbow and rub in three times daily.
For diagnosis: A drop of the blood to be tested is mixed with a drop of the
Polysan antigens specified for the particular testing. Macroscopically
and microscopically visible agglutination occurs in the case of antigen-
antibody reaction. At the same time, the degree of agglutination is an
indicator of the level of antibody titer.

164
Side effects: None known. Because of specific organic components of Polysan D,
theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage form is available: 10 ml dropper bottle 9X.

165
Polysan Dx 9X
Drops
Liquid dilution
for diagnosis, rubbing in

Active ingredient: Spengler colloid Dx 9X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Spengler colloid Dx 9X according to Dr. Carl Spengler with antigens
from Streptococcus lanceolatus, Staphylococcus aureus, Diplococcus
pneumonia as well as with the respective antitoxins from the blood of
highly immunized rabbits.

According to experience, Latent focal infections (in alternation with Polysan D).
to be administered in
cases of:

Characteristics: The Polysans can be used therapeutically and also diagnostically.


In chronic diseases such as tuberculosis, rheumatism, cancer, etc.,
Carl Spengler, M.D., isolated gram-positive and gram-negative granula
from erythrocytes which he described as blood parasites. According
to Spengler, the gram-positive malignant granula disturb the binding
of oxygen to hemoglobin by their fermentation, thus endangering the
formation of defensive substances. It was his conviction that erythrocytes
infested with granula are the carriers of both inherited and endogenic
toxins. These specific inherited allergies are transferred from the mother
blood onto the child and may burden the descendants over several
generations. After cultivating the granula in special culture-media, Dr.
Spengler produced a vaccine which, in its homeopathically potentized
form, was suitable as a therapeutic agent for chronic infections and for
active immunization. When antibodies are present in human blood due
to a former disease, they react with the respective Spengler-colloid in
the sense of an antigen-antibody-reaction. This reaction is used in the
diagnostic blood test (developed by Schwarz). By using the Polysans
the body is stimulated to an intensified specific immune defense. It must
be noted that local complaints do not necessarily indicate chronic foci.
However, these must in each case be therapeutically treated, because
they are permanent disturbance fields and, as such, they block the
endogenic regulation of the organism.

Application: Unless otherwise prescribed: For rubbing in: apply 5-10 drops into the
bend of the elbow and rub in three times daily.
For diagnosis: A drop of the blood to be tested is mixed with a drop of the
Polysan antigens specified for the particular testing. Macroscopically
and microscopically visible agglutination occurs in the case of antigen-
antibody reaction. At the same time, the degree of agglutination is an
indicator of the level of antibody titer.

166
Side effects: None known. Because of specific organic components of Polysan
Dx, theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage form is available: 10 ml dropper bottle 9X.

167
Polysan E 9X
Drops
Liquid dilution
for diagnosis, rubbing in

Active ingredient: Spengler colloid E 9X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Spengler colloid E 9X according to Dr. Carl Spengler with antigens
from luetic hereditary toxins as well as with the respective antitoxins
from the blood of highly immunized rabbits.

According to experience, Inherited toxins, especially of luetic nature; for reduction of minor
to be administered in inflammation.
cases of:

Characteristics: The Polysans can be used therapeutically and also diagnostically.


In chronic diseases such as tuberculosis, rheumatism, cancer, etc.,
Carl Spengler, M.D., isolated gram-positive and gram-negative granula
from erythrocytes which he described as blood parasites. According
to Spengler, the gram-positive malignant granula disturb the binding
of oxygen to hemoglobin by their fermentation, thus endangering the
formation of defensive substances. It was his conviction that erythrocytes
infested with granula are the carriers of both inherited and endogenic
toxins. These specific inherited allergies are transferred from the mother
blood onto the child and may burden the descendants over several
generations. After cultivating the granula in special culture-media, Dr.
Spengler produced a vaccine which, in its homeopathically potentized
form, was suitable as a therapeutic agent for chronic infections and for
active immunization. When antibodies are present in human blood due
to a former disease, they react with the respective Spengler-colloid in
the sense of an antigen-antibody-reaction. This reaction is used in the
diagnostic blood test (developed by Schwarz). By using the Polysans
the body is stimulated to an intensified specific immune defense. It must
be noted that local complaints do not necessarily indicate chronic foci.
However, these must in each case be therapeutically treated, because
they are permanent disturbance fields and, as such, they block the
endogenic regulation of the organism.

Application: Unless otherwise prescribed: For rubbing in: apply 5-10 drops into the
bend of the elbow and rub in three times daily.
For diagnosis: A drop of the blood to be tested is mixed with a drop of the
Polysan antigens specified for the particular testing. Macroscopically
and microscopically visible agglutination occurs in the case of antigen-
antibody reaction. At the same time, the degree of agglutination is an
indicator of the level of antibody titer.

168
Side effects: None known. Because of specific organic components of Polysan E,
theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage form is available: 10 ml dropper bottle 9X.

169
Polysan G 9X
Drops
Liquid dilution
for diagnosis, rubbing in

Active ingredient: Spengler colloid G 9X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Spengler colloid G 9X according to Dr. Carl Spengler with antigens
from Virus influenzae Spengler, Bazillus influenzae Pfeiffer, Bacterium
pneumoniae as well as with the respective antitoxins from the blood of
highly immunized rabbits.

According to experience, Flu, angina, suppurations, all inflammations, blood poisoning, feverish
to be administered in diseases, diverse colds.
cases of:

Characteristics: The Polysans can be used therapeutically and also diagnostically.


In chronic diseases such as tuberculosis, rheumatism, cancer, etc.,
Carl Spengler, M.D., isolated gram-positive and gram-negative granula
from erythrocytes which he described as blood parasites. According
to Spengler, the gram-positive malignant granula disturb the binding
of oxygen to hemoglobin by their fermentation, thus endangering the
formation of defensive substances. It was his conviction that erythrocytes
infested with granula are the carriers of both inherited and endogenic
toxins. These specific inherited allergies are transferred from the mother
blood onto the child and may burden the descendants over several
generations. After cultivating the granula in special culture-media, Dr.
Spengler produced a vaccine which, in its homeopathically potentized
form, was suitable as a therapeutic agent for chronic infections and for
active immunization. When antibodies are present in human blood due
to a former disease, they react with the respective Spengler-colloid in
the sense of an antigen-antibody-reaction. This reaction is used in the
diagnostic blood test (developed by Schwarz). By using the Polysans
the body is stimulated to an intensified specific immune defense. It must
be noted that local complaints do not necessarily indicate chronic foci.
However, these must in each case be therapeutically treated, because
they are permanent disturbance fields and, as such, they block the
endogenic regulation of the organism.

Application: Unless otherwise prescribed: For rubbing in: apply 5-10 drops into the
bend of the elbow and rub in three times daily.
For diagnosis: A drop of the blood to be tested is mixed with a drop of the
Polysan antigens specified for the particular testing. Macroscopically
and microscopically visible agglutination occurs in the case of antigen-
antibody reaction. At the same time, the degree of agglutination is an
indicator of the level of antibody titer.

170
Side effects: None known. Because of specific organic components of Polysan G,
theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage form is available: 10 ml dropper bottle 9X.

171
Polysan K 9X
Drops
Liquid dilution
for diagnosis, rubbing in

Active ingredient: Spengler colloid K 9X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Spengler colloid K 9X according to Dr. Carl Spengler with antigens
from Streptococcus lanceolatus, Staphylococcus aureus, Diplococcus
pneumoniae as well as with the respective antitoxins from the blood of
highly immunized rabbits.

According to experience, Circulatory disorders, venous congestion, varicose veins; allergic


to be administered in illnesses (asthma, hay fever), pre-cancerous stages.
cases of:

Characteristics: The Polysans can be used therapeutically and also diagnostically.


In chronic diseases such as tuberculosis, rheumatism, cancer, etc.,
Carl Spengler, M.D., isolated gram-positive and gram-negative granula
from erythrocytes which he described as blood parasites. According
to Spengler, the gram-positive malignant granula disturb the binding
of oxygen to hemoglobin by their fermentation, thus endangering the
formation of defensive substances. It was his conviction that erythrocytes
infested with granula are the carriers of both inherited and endogenic
toxins. These specific inherited allergies are transferred from the mother
blood onto the child and may burden the descendants over several
generations. After cultivating the granula in special culture-media, Dr.
Spengler produced a vaccine which, in its homeopathically potentized
form, was suitable as a therapeutic agent for chronic infections and for
active immunization. When antibodies are present in human blood due
to a former disease, they react with the respective Spengler-colloid in
the sense of an antigen-antibody-reaction. This reaction is used in the
diagnostic blood test (developed by Schwarz). By using the Polysans
the body is stimulated to an intensified specific immune defense. It must
be noted that local complaints do not necessarily indicate chronic foci.
However, these must in each case be therapeutically treated, because
they are permanent disturbance fields and, as such, they block the
endogenic regulation of the organism.

Application: Unless otherwise prescribed: For rubbing in: apply 5-10 drops into the
bend of the elbow and rub in three times daily.
For diagnosis: A drop of the blood to be tested is mixed with a drop of the
Polysan antigens specified for the particular testing. Macroscopically
and microscopically visible agglutination occurs in the case of antigen-
antibody reaction. At the same time, the degree of agglutination is an
indicator of the level of antibody titer.

172
Side effects: None known. Because of specific organic components of Polysan K,
theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage form is available: 10 ml dropper bottle 9X.

173
Polysan M 9X
Drops
Liquid dilution
for diagnosis, rubbing in

Active ingredient: Spengler colloid M 9X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Spengler colloid M 9X according to Dr. Carl Spengler with antigens
from Malaria plasmodia as well as with the respective antitoxins from
the blood of highly immunized rabbits.

According to experience, Malaria and its late effects; fever.


to be administered in
cases of:

Characteristics: The Polysans can be used therapeutically and also diagnostically.


In chronic diseases such as tuberculosis, rheumatism, cancer, etc.,
Carl Spengler, M.D., isolated gram-positive and gram-negative granula
from erythrocytes which he described as blood parasites. According
to Spengler, the gram-positive malignant granula disturb the binding
of oxygen to hemoglobin by their fermentation, thus endangering the
formation of defensive substances. It was his conviction that erythrocytes
infested with granula are the carriers of both inherited and endogenic
toxins. These specific inherited allergies are transferred from the mother
blood onto the child and may burden the descendants over several
generations. After cultivating the granula in special culture-media, Dr.
Spengler produced a vaccine which, in its homeopathically potentized
form, was suitable as a therapeutic agent for chronic infections and for
active immunization. When antibodies are present in human blood due
to a former disease, they react with the respective Spengler-colloid in
the sense of an antigen-antibody-reaction. This reaction is used in the
diagnostic blood test (developed by Schwarz). By using the Polysans
the body is stimulated to an intensified specific immune defense. It must
be noted that local complaints do not necessarily indicate chronic foci.
However, these must in each case be therapeutically treated, because
they are permanent disturbance fields and, as such, they block the
endogenic regulation of the organism.

Application: Unless otherwise prescribed: For rubbing in: apply 5-10 drops into the
bend of the elbow and rub in three times daily.
For diagnosis: A drop of the blood to be tested is mixed with a drop of the
Polysan antigens specified for the particular testing. Macroscopically
and microscopically visible agglutination occurs in the case of antigen-
antibody reaction. At the same time, the degree of agglutination is an
indicator of the level of antibody titer.

174
Side effects: None known. Because of specific organic components of Polysan M,
theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage form is available: 10 ml dropper bottle 9X.

175
Polysan Om 9X
Drops
Liquid dilution
for diagnosis, rubbing in

Active ingredient: Spengler colloid Om 9X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Spengler colloid Om 9X according to Dr. Carl Spengler with
antigens from Streptococcus lacticus, pyogenes, hemolyticus, viridans,
Staphylococcus albus, pharyngis, aureus, Diplococcus lanceolatus,
Mycobacterium tuberculosis typus bovinus as well as with the respective
antitoxins from the blood of highly immunized rabbits.

According to experience, Skin conditions, such as warts and moles; neoplasms, both benign
to be administered in and malignant, precancerosis.
cases of:

Characteristics: The Polysans can be used therapeutically and also diagnostically.


In chronic diseases such as tuberculosis, rheumatism, cancer, etc.,
Carl Spengler, M.D., isolated gram-positive and gram-negative granula
from erythrocytes which he described as blood parasites. According
to Spengler, the gram-positive malignant granula disturb the binding
of oxygen to hemoglobin by their fermentation, thus endangering the
formation of defensive substances. It was his conviction that erythrocytes
infested with granula are the carriers of both inherited and endogenic
toxins. These specific inherited allergies are transferred from the mother
blood onto the child and may burden the descendants over several
generations. After cultivating the granula in special culture-media, Dr.
Spengler produced a vaccine which, in its homeopathically potentized
form, was suitable as a therapeutic agent for chronic infections and for
active immunization. When antibodies are present in human blood due
to a former disease, they react with the respective Spengler-colloid in
the sense of an antigen-antibody-reaction. This reaction is used in the
diagnostic blood test (developed by Schwarz). By using the Polysans
the body is stimulated to an intensified specific immune defense. It must
be noted that local complaints do not necessarily indicate chronic foci.
However, these must in each case be therapeutically treated, because
they are permanent disturbance fields and, as such, they block the
endogenic regulation of the organism.

Application: Unless otherwise prescribed: For rubbing in: apply 5-10 drops into the
bend of the elbow and rub in three times daily.
For diagnosis: A drop of the blood to be tested is mixed with a drop of the
Polysan antigens specified for the particular testing. Macroscopically
and microscopically visible agglutination occurs in the case of antigen-
antibody reaction. At the same time, the degree of agglutination is an
indicator of the level of antibody titer.

176
Side effects: None known. Because of specific organic components of Polysan
Om, theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage form is available: 10 ml dropper bottle 9X.

177
Polysan R 9X
Drops
Liquid dilution
for diagnosis, rubbing in

Active ingredient: Spengler colloid R 9X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Spengler colloid R 9X according to Dr. Carl Spengler with antigens
from Mycobacterium tuberculosis typus brevis, Mycobacterium
tuberculosis typus bovinus, Streptococcus pyogenes as well as with
the respective antitoxins from the blood of highly immunized rabbits.

According to experience, Rheumatism, arthritis, gout, neuralgia, elimination of uric acid, rheuma-
to be administered in tism of tuberculous origin.
cases of:

Characteristics: The Polysans can be used therapeutically and also diagnostically.


In chronic diseases such as tuberculosis, rheumatism, cancer, etc.,
Carl Spengler, M.D., isolated gram-positive and gram-negative granula
from erythrocytes which he described as blood parasites. According
to Spengler, the gram-positive malignant granula disturb the binding
of oxygen to hemoglobin by their fermentation, thus endangering the
formation of defensive substances. It was his conviction that erythrocytes
infested with granula are the carriers of both inherited and endogenic
toxins. These specific inherited allergies are transferred from the mother
blood onto the child and may burden the descendants over several
generations. After cultivating the granula in special culture-media, Dr.
Spengler produced a vaccine which, in its homeopathically potentized
form, was suitable as a therapeutic agent for chronic infections and for
active immunization. When antibodies are present in human blood due
to a former disease, they react with the respective Spengler-colloid in
the sense of an antigen-antibody-reaction. This reaction is used in the
diagnostic blood test (developed by Schwarz). By using the Polysans
the body is stimulated to an intensified specific immune defense. It must
be noted that local complaints do not necessarily indicate chronic foci.
However, these must in each case be therapeutically treated, because
they are permanent disturbance fields and, as such, they block the
endogenic regulation of the organism.

Application: Unless otherwise prescribed: For rubbing in: apply 5-10 drops into the
bend of the elbow and rub in three times daily.
For diagnosis: A drop of the blood to be tested is mixed with a drop of the
Polysan antigens specified for the particular testing. Macroscopically
and microscopically visible agglutination occurs in the case of antigen-
antibody reaction. At the same time, the degree of agglutination is an
indicator of the level of antibody titer.

178
Side effects: None known. Because of specific organic components of Polysan R,
theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage form is available: 10 ml dropper bottle 9X.

179
Polysan T 9X
Drops
Liquid dilution
for diagnosis, rubbing in

Active ingredient: Spengler colloid T 9X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Spengler colloid T 9X according to Dr. Carl Spengler with antigens
from Mycobacterium tuberculosis typus humanus, Mycobacterium
tuberculosis typus brevis, Mycobacterium tuberculosis typus bovinus,
Diplococcus pneumoniae, Streptococcus mucosus as well as with the
respective antitoxins from the blood of highly immunized rabbits.

According to experience, Tuberculosis, its latent and masked forms as asthma, eczema, rheuma-
to be administered in tism, arthritis, migraine, scrofulosis.
cases of:

Characteristics: The Polysans can be used therapeutically and also diagnostically.


In chronic diseases such as tuberculosis, rheumatism, cancer, etc.,
Carl Spengler, M.D., isolated gram-positive and gram-negative granula
from erythrocytes which he described as blood parasites. According
to Spengler, the gram-positive malignant granula disturb the binding
of oxygen to hemoglobin by their fermentation, thus endangering the
formation of defensive substances. It was his conviction that erythrocytes
infested with granula are the carriers of both inherited and endogenic
toxins. These specific inherited allergies are transferred from the mother
blood onto the child and may burden the descendants over several
generations. After cultivating the granula in special culture-media, Dr.
Spengler produced a vaccine which, in its homeopathically potentized
form, was suitable as a therapeutic agent for chronic infections and for
active immunization. When antibodies are present in human blood due
to a former disease, they react with the respective Spengler-colloid in
the sense of an antigen-antibody-reaction. This reaction is used in the
diagnostic blood test (developed by Schwarz). By using the Polysans
the body is stimulated to an intensified specific immune defense. It must
be noted that local complaints do not necessarily indicate chronic foci.
However, these must in each case be therapeutically treated, because
they are permanent disturbance fields and, as such, they block the
endogenic regulation of the organism.

Application: Unless otherwise prescribed: For rubbing in: apply 5-10 drops into the
bend of the elbow and rub in three times daily.
For diagnosis: A drop of the blood to be tested is mixed with a drop of the
Polysan antigens specified for the particular testing. Macroscopically
and microscopically visible agglutination occurs in the case of antigen-
antibody reaction. At the same time, the degree of agglutination is an
indicator of the level of antibody titer.

180
Side effects: None known. Because of specific organic components of Polysan T,
theoretically, hypersensitivity may occur. In this case, discontinue
medication and treat symptomatically.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage form is available: 10 ml dropper bottle 9X.

181
Quentakehl 3X
Suppositories
for rectal application

Active ingredient: Penicillium glabrum e volumine cellulae (lyophil., steril.) 3X

Composition: 1 suppository contains: Medically active substance: 0.2 g Penicillium


glabrum e volumine cellulae (lyophil., steril.) 3X trit. Other
constituents: hard fat, lactose.

According to experience, Acute and latent viral infections, e.g. laryngitis, bronchitis, sinusitis, pharyn-
to be administered in gitis, influenzal infections; all diseases caused by mixed caused by
cases of: mixed infections, e.g. Herpes zoster, chicken pox; migraine; multiple
sclerosis; vertigo; Menires disease.

Characteristics: Quentakehl is obtained from the mold fungus Penicillium glabrum.


Quentakehl is administered in all cases of viral disorders. It is not an
antibiotic and does not produce antibiotic substances. Therefore, there
are no side effects like those which may occur during treatment with
antibiotics, such as allergies, liver damages, destruction of intestinal
flora and the formation of Penicillin resistant strains.

Application: Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally.

Side effects: Because of specific organic components of Quentakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Penicillium glabrum).

Adverse reactions: None known.

Interactions
with other remedies: Immunosuppressive drugs can influence the effectivity of Quentakehl.
An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

182
Additional advice: Penicillium glabrum as an active ingredient is also contained in
Nota-Quent.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

183
Quentakehl 4X
Capsules
for oral intake

Active ingredient: Penicillium glabrum e volumine cellulae (lyophil., steril.) 4X

Composition: 1 capsule contains: Medically active substance: 330 mg Penicillium


glabrum e volumine cellulae 4X trit. Other constituents: lactose,
hypromellosis (capsule shell).

According to experience, Acute and latent viral infections, e.g. laryngitis, bronchitis, sinusitis, pharyn-
to be administered in gitis, influenzal infections; all diseases caused by mixed infections, e.g.
cases of: Herpes zoster, chicken pox; migraine; multiple sclerosis; vertigo;
Menires disease.

Characteristics: Quentakehl is obtained from the mold fungus Penicillium glabrum.


Quentakehl is administered in all cases of viral disorders. It is not an
antibiotic and does not produce antibiotic substances. Therefore, there
are no side effects like those which may occur during treatment with
antibiotics, such as allergies, liver damages, destruction of intestinal
flora and the formation of Penicillin resistant strains.

Application: Unless otherwise prescribed: 1-3 x daily 1 capsule.

Side effects: Because of specific organic components of Quentakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Penicillium glabrum).

Adverse reactions: None known.

Interactions with
other remedies: Immunosuppressive drugs can influence the effectivity of Quentakehl.
An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

184
Additional advice: Penicillium glabrum as an active ingredient is also contained in
Nota-Quent.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

185
Quentakehl 5X
Ampules
Liquid dilution for injection

Active ingredient: Penicillium glabrum e volumine cellulae (lyophil., steril.) 5X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Penicillium


glabrum e volumine cellulae (lyophil., steril.) 5X aquous dil.
Other constituents: isotonic sodium chloride solution.

According to experience, Acute and latent viral infections, e.g. laryngitis, bronchitis, sinusitis, pharyn-
to be administered in gitis, influenzal infections; all diseases caused by mixed infections,
cases of: e.g. Herpes zoster, chicken pox; migraine; multiple sclerosis; vertigo;
Menires disease.

Characteristics: Quentakehl is obtained from the mold fungus Penicillium glabrum.


Quentakehl is administered in all cases of viral disorders. It is not an
antibiotic and does not produce antibiotic substances. Therefore, there
are no side effects like those which may occur during treatment with
antibiotics, such as allergies, liver damages, destruction of intestinal
flora and the formation of Penicillin resistant strains.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3
x weekly.

Side effects: Because of specific organic components of Quentakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Penicillium glabrum).

Adverse reactions: None known.

Interactions
with other remedies: Immunosuppressive drugs can influence the effectivity of Quentakehl.
An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: None.

186
Additional advice: Penicillium glabrum as an active ingredient is also contained in
Nota-Quent.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

187
Quentakehl 5X
Drops
Liquid dilution
for oral intake, rubbing in, inhalation

Active ingredient: Penicillium glabrum e volumine cellulae (lyophil., steril.) 5X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Penicillium glabrum e volumine cellulae (lyophil., steril.) 5X
dil. Other constituents: purified water.

According to experience, Acute and latent viral infections, e.g. laryngitis, bronchitis, sinusitis, pharyn-
to be administered in gitis, influenzal infections; all diseases caused by mixed infections,
cases of: e.g. Herpes zoster, chicken pox; migraine; multiple sclerosis; vertigo;
Menires disease.

Characteristics: Quentakehl is obtained from the mold fungus Penicillium glabrum.


Quentakehl is administered in all cases of viral disorders. It is not an
antibiotic and does not produce antibiotic substances. Therefore, there
are no side effects like those which may occur during treatment with
antibiotics, such as allergies, liver damages, destruction of intestinal
flora and the formation of Penicillin resistant strains.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops.
For rubbing in: 1 x daily 5-10 drops into the bend of the elbow. For
inhalation: 10-20 drops, inhaled deeply 2-3 x daily.

Side effects: Because of specific organic components of Quentakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Penicillium glabrum).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Quentakehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: After opening, contents must be used within two months.

188
Additional advice: Penicillium glabrum as an active ingredient is also contained in
Nota-Quent.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

189
Rebas 4X
Capsules
for oral intake

Active ingredient: Folliculi lymphatici aggregati (lyophil., steril.) 4X

Composition: 1 capsule contains: Medically active substance: 330 mg Folliculi


lymphatici aggregati (lyophil., steril.) 4X trit. Other constituents:
lactose, hypromellosis (capsule shell).

According to experience, Chronic and recurrent inflammations which include disorders of the
to be administered in humoral body defense, gastrointestinal diseases, chronic hepatitis,
cases of: tonsillitis.

Characteristics: Rebas is produced from Peyers Patches which are a significant part
of the immune system. It is applied for strengthening humoral immunity
and activating immune support.

Application: Unless otherwise prescribed: 1-3 x daily 1 capsule.

Side effects: Because of specific organic components of Rebas, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,


especially pork protein.

Adverse reactions: None known.


with other remedies:

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 2 ml ampule 10 and 50 5X,
12X, 10 suppositories 4X, 6X, 20 capsules 4X, 6X.

190
Rebas 4X
Suppositories
for rectal application

Active ingredient: Folliculi lymphatici aggregati (lyophil., steril.) 4X

Composition: 1 suppository contains: Medically active substance: 0.2 g Folliculi


lymphatici aggregati (lyophil., steril.) 4X trit. Other constituents:
hard fat, lactose.

According to experience, Chronic and recurrent inflammations which include disorders of the
to be administered in humoral body defense, gastrointestinal diseases, chronic hepatitis,
cases of: tonsillitis.

Characteristics: Rebas is produced from Peyers Patches which are a significant part
of the immune system. It is applied for strengthening humoral immunity
and activating immune support.

Application: Unless otherwise prescribed: 1 x daily insert 1 suppository rectally.

Side effects: Because of specific organic components of Rebas, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,


especially pork protein.

Adverse reactions: None known.

Interactions None known.


with other remedies:

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 2 ml ampule 10 and 50 5X,
12X, 10 suppositories 4X, 6X, 20 capsules 4X, 6X.

191
Rebas 5X
Ampules
Liquid dilution for injection

Active ingredient: Folliculi lymphatici aggregati (lyophil., steril.) 5X

Composition: 1 ampule of 2 ml contains: Medically active substance: 2 ml Folliculi


lymphatici aggregati (lyophil., steril.) 5X aquous dil. Other
constituents: isotonic sodium chloride solution.

According to experience, Chronic and recurrent inflammations which include disorders of the
to be administered in humoral body defense, gastrointestinal diseases, chronic hepatitis,
cases of: tonsillitis.

Characteristics: Rebas is produced from Peyers Patches which are a significant part
of the immune system. It is applied for strengthening humoral immunity
and activating immune support.

Application: Unless otherwise prescribed: 1 ampule of 2 ml to be injected either


intramuscularly, subcutaneously or intracutaneously, 1-3 x weekly.

Side effects: Because of specific organic components of Rebas, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,


especially pork protein.

Adverse reactions: None known.

Interactions None known.


with other remedies:

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 2 ml ampule 10 and 50 5X,
12X, 10 suppositories 4X, 6X, 20 capsules 4X, 6X.

192
Rebas 6X
Capsules
for oral intake

Active ingredient: Folliculi lymphatici aggregati (lyophil., steril.) 6X

Composition: 1 capsule contains: Medically active substance: 330 mg Folliculi


lymphatici aggregati (lyophil., steril.) 6X trit. Other constituents:
lactose, hypromellosis (capsule shell).

According to experience, Chronic and recurrent inflammations which include disorders of the
to be administered in humoral body defense, gastrointestinal diseases, chronic hepatitis,
cases of: tonsillitis.

Characteristics: Rebas is produced from Peyers Patches which are a significant part
of the immune system. It is applied for strengthening humoral immunity
and activating immune support.

Application: Unless otherwise prescribed: 1-3 x daily 1 capsule.

Side effects: Because of specific organic components of Rebas, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,


especially pork protein.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 2 ml ampule 10 and 50 5X,
12X, 10 suppositories 4X, 6X, 20 capsules 4X, 6X.

193
Rebas 6X
Suppositories
for rectal application

Active ingredient: Folliculi lymphatici aggregati (lyophil., steril.) 6X

Composition: 1 suppository contains: Medically active substance: 0.2 g Folliculi


lymphatici aggregati (lyophil., steril.) 6X trit. Other constituents:
hard fat, lactose.

According to experience, Chronic and recurrent inflammations which include disorders of the
to be administered in humoral body defense, gastrointestinal diseases, chronic hepatitis,
cases of: tonsillitis.

Characteristics: Rebas is produced from Peyers Patches which are a significant part
of the immune system. It is applied for strengthening humoral immunity
and activating immune support.

Application: Unless otherwise prescribed: 1 x daily insert 1 suppository rectally.

Side effects: Because of specific organic components of Rebas, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,


especially pork protein.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This products contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 2 ml ampule 10 and 50 5X,
12X, 10 suppositories 4X, 6X, 20 capsules 4X, 6X.

194
Rebas 12X
Ampules
Liquid dilution for injection

Active ingredient: Folliculi lymphatici aggregati (lyophil., steril.) 12X

Composition: 1 ampule of 2 ml contains: Medically active substance: 2 ml Folliculi


lymphatici aggregati (lyophil., steril.) 12X aquous dil. Other con-
stituents: isotonic sodium chloride solution.

According to experience, Chronic and recurrent inflammations which include disorders of the
to be administered in humoral body defense, gastrointestinal diseases, chronic hepatitis,
cases of: tonsillitis.

Characteristics: Rebas is produced from Peyers Patches which are a significant part
of the immune system. It is applied for strengthening humoral immunity
and activating immune support.

Application: Unless otherwise prescribed: 1 ampule of 2 ml to be injected either


intramuscularly, subcutaneously or intracutaneously, 1-3 x weekly.

Side effects: Because of specific organic components of Rebas, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,


especially pork protein.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 2 ml ampule 10 and 50 5X,
12X, 10 suppositories 4X, 6X, 20 capsules 4X, 6X.

195
Recarcin 4X
Ampules
Liquid dilution for injection

Active ingredient: Bacillus firmus e volumine cellulae (lyophil., steril.) 4X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1ml Bacillus


firmus e volumine cellulae (lyophil., steril.) 4X aquous dil.. Other
constituents: isotonic sodium chloride solution.

According to experience, All subacute and chronic inflammatory diseases, especially of the
to be administered in glands and serosae; arthritis and arthrosis; susceptibility to infection
cases of: (for immune modulation).

Characteristics: Recarcin is produced from the non-pathogenic microbe Bacillus


firmus. It is applied for immune modulation, especially in chronic
infections.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously or intracutaneously, 1-2 x weekly.

Side effects: Because of specific organic components of Recarcin, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


In cases of known hypersensitivity to Bacillus firmus, as a precaution,
this preparation should not be administered.

Adverse reactions: None known. Generally well tolerated. Occasionally local reactions
like rubefaction, swelling or painfulness may be observed, normally
vanishing without treatment. These effects are not to be seen as
adverse reactions, but rather as an expression of effectiveness. In the
first 2 or 3 days after the injection sometimes conditions of weakness,
fortified expectoration, slight painfulness of the region or subfebrile
temperatures may show. Strong general reactions are always a sign of
overdose or of incorrect injection technique.

Interactions Immunosuppressive drugs can influence the effectivity of Recarcin.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

196
Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

197
Recarcin 4X
Capsules
for oral intake

Active ingredient: Bacillus firmus e volumine ex muris cellulae (lyophil., steril.) 4X

Composition: 1 capsule contains: Medically active substance: 330 mg Bacillus


firmus e volumine ex murae cellulae (lyophil., steril.) 4X trit.
Other constituents: lactose, hypromellosis (capsule shell).

According to experience, All subacute and chronic inflammatory diseases, especially of the
to be administered in glands and serosae; arthritis and arthrosis; susceptibility to infection
cases of: (for immune modulation).

Characteristics: Recarcin is produced from the non-pathogenic microbe Bacillus


firmus. It is applied for immune modulation, especially in chronic
infections.

Application: Unless otherwise prescribed: 1-2 x weekly 1 capsule.

Side effects: Because of specific organic components of Recarcin, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


In cases of known hypersensitivity to Bacillus firmus, as a precaution,
this preparation should not be administered.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Recarcin.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

198
Recarcin 6X
Ampules
Liquid dilution for injection

Active ingredient: Bacillus firmus e volumine cellulae (lyophil., steril.) 6X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Bacillus


firmus e volumine cellulae (lyophil., steril.) 6X aquous dil. Other
constituents: isotonic sodium chloride solution.

According to experience, All subacute and chronic inflammatory diseases, especially of the
to be administered in glands and serosae; arthritis and arthrosis; susceptibility to infection
cases of: (for immune modulation).

Characteristics: Recarcin is produced from the non-pathogenic microbe Bacillus


firmus. It is applied for immune modulation, especially in chronic
infections.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously or intracutaneously, 1-2 x weekly.

Side effects: Because of specific organic components of Recarcin, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


In cases of known hypersensitivity to Bacillus firmus, as a precaution,
this preparation should not be administered.

Adverse reactions: None known. Generally well tolerated. Occasionally local reactions
like rubefaction, swelling or painfulness may be observed, normally
vanishing without treatment. These effects are not to be seen as
adverse reactions, but rather as an expression of effectiveness. In the
first 2 or 3 days after the injection sometimes conditions of weakness,
fortified expectoration, slight painfulness of the region or subfebrile
temperatures may show. Strong general reactions are always a sign of
overdose or of incorrect injection technique.

Interactions Immunosuppressive drugs can influence the effectivity of Recarcin.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

199
Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

200
Recarcin 6X
Capsules
for oral intake

Active ingredient: Bacillus firmus e volumine ex muris cellulae (lyophil., steril.) 6X

Composition: 1 capsule contains: Medically active substance: 330 mg Bacillus firmus


e volumine ex muris cellulae (lyophil., steril.) 6X trit. Other
constituents: lactose, hypromellosis (capsule shell).

According to experience, All subacute and chronic inflammatory diseases, especially of the
to be administered in glands and serosae; arthritis and arthrosis; susceptibility to infection
cases of: (for immune modulation).

Characteristics: Recarcin is produced from the non-pathogenic microbe Bacillus


firmus. It is applied for immune modulation, especially in chronic
infections.

Application: Unless otherwise prescribed: 1-2 x weekly 1 capsule.

Side effects: Because of specific organic components of Recarcin, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


In cases of known hypersensitivity to Bacillus firmus, as a precaution,
this preparation should not be administered.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Recarcin.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

201
Recarcin 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Bacillus firmus e volumine cellulae (lyophil., steril.) 6X

Composition: 5 ml liquid dilution contain: Medically active substance: 5 ml Bacillus


firmus e volumine cellulae (lyophil., steril.) 6X dil. Other con-
stituents: purified water.

According to experience, All subacute and chronic inflammatory diseases, especially of the
to be administered in glands and serosae; arthritis and arthrosis; susceptibility to infection
cases of: (for immune modulation).

Characteristics: Recarcin is produced from the non-pathogenic microbe Bacillus


firmus. It is applied for immune modulation, especially in chronic
infections.

Application: Unless otherwise prescribed: For oral intake: 1-3 x weekly 2-5 drops
before a meal. For rubbing in: 1-3 x weekly 2-5 drops into the bend of
the elbow.

Side effects: Because of specific organic components of Recarcin, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


In cases of known hypersensitivity to Bacillus firmus, as a precaution,
this preparation should not be administered.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Recarcin.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: After opening, contents must be used within two months.

202
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

203
Recarcin 6X
Suppositories
for rectal application

Active ingredient: Bacillus firmus e volumine ex muris cellulae (lyophil., steril.) 6X

Composition: 1 suppository contains: Medically active substance: 0.2 g Bacillus


firmus e volumine ex muris cellulae cellulae (lyophil., steril.)
6X trit. Other constituents: hard fat, lactose.

According to experience, All subacute and chronic inflammatory diseases, especially of the
to be administered in glands and serosae; arthritis and arthrosis; susceptibility to infection
cases of: (for immune modulation).

Characteristics: Recarcin is produced from the non-pathogenic microbe Bacillus


firmus. It is applied for immune modulation, especially in chronic
infections.

Application: Unless otherwise prescribed: 1-3 x weekly insert 1 suppository.

Side effects: Because of specific organic components of Recarcin, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


In cases of known hypersensitivity to Bacillus firmus, as a precaution,
this preparation should not be administered.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Recarcin.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

204
Relivora Complex
Ampules
Liquid dilution for injection

Active ingredients: Drosera 3X, Echinacea angustifolia 4X, Juglans 4X

Composition: 1 ampule of 2 ml contains: Medically active substance: 50.0 l Drosera


rotundifolia 3X aquous dil., 500 l Echinacea angustifolia 4X
aquous dil., 500 l Juglans 4X aquous dil. Other constituents: isotonic
sodium chloride solution.

According to experience, Stimulation of the bodys immune system; fever; inflammatory processes
to be administered in of the respiratory tract (hard, dry cough), bronchitis, whooping
cases of: cough.

Characteristics: The individual components of Relivora Complex have the following


significance: Extracts from Drosera have broncholytic, secretolytic
and spasmolytic properties. Echinacea angustifolia is administered
for support of the bodys non specific defense system, in cases of
resistance to antibiotics, recurring infections and inflammatory processes
in the area of the urogenital system, ENT (ear, nose and throat) and
dermatology. The high tannin content in Juglans explains its use as
antiscrofulosum. It is predominantly used externally for skin disorders
such as acne, eczema, pyodermia and ulcers. The essential oil has
antifungal properties, whilst the watery extract shows antiviral effects
in tissue cultures. Relivora Complex is a well-balanced combination
of drugs containing naphthoquinone (Drosera and Juglans) with the
immune stimulating factors of Echinacea.

Application: Unless otherwise prescribed: 1 ampule of 2 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1 x
daily.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Occasionally signs of a hypersensitivity reaction may occur. For drugs
containing Echinacea, symptoms like skin irritation, itching, facial
swelling, shortness of breath, dizziness, drop in blood pressure are
known.

Contraindications: This preparation should not be administered if cases of hypersensitivity


to any of the ingredients, exipients or compositae are known.
Furthermore, it should not be administered in patients with alcohol
problems or because of the ingredient Echinacea with progressive
systemic diseases such as tuberculosis, leucosis, inflammatory diseases
of the connective tissue (collagenosis), autoimmune diseases, multiple
sclerosis, AIDS, HIV infections and other chronic viral illnesses.

205
Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 30 ml and 100 ml dropper
bottle 3X/2X/4X, 2 ml ampule 10 and 50 3X/4X/4X.

206
Relivora Complex
Drops
Liquid dilution
for oral intake

Active ingredients: Drosera 3X, Echinacea angustifolia 2X, Juglans 4X

Composition: 10 ml liquid dilution contain: Medically active substance: 0.25 ml


Drosera 3X dil., 0.025 ml Echinacea angustifolia 2X dil., 2.5 ml
Juglans 4X dil. Other constituents: ethanol 22.17 % (m/m), purified
water.

According to experience, Stimulation of the bodys immune system; fever; inflammatory processes
to be administered in of the respiratory tract (hard, dry cough), bronchitis, whooping cough.
cases of:

Characteristics: The individual components of Relivora Complex have the following


significance: Extracts from Drosera have broncholytic, secretolytic
and spasmolytic properties. Echinacea angustifolia is administered
for support of the bodys non specific defense system, in cases of
resistance to antibiotics, recurring infections and inflammatory processes
in the area of the urogenital system, ENT (ear, nose and throat) and
dermatology. The high tannin content in Juglans explains its use as
antiscrofulosum. It is predominantly used externally for skin disorders
such as acne, eczema, pyodermia and ulcers. The essential oil has
antifungal properties, whilst the watery extract shows antiviral effects
in tissue cultures. Relivora Complex is a well-balanced combination
of drugs containing naphthoquinone (Drosera and Juglans) with the
immune stimulating factors of Echinacea.

Application: Unless otherwise prescribed: For oral intake: In case of acute conditions
15 drops every two hours, up to 6 times daily. In case of chronic
conditions 20-25 drops, 3 times daily.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Occasionally signs of a hypersensitivity reaction may occur. For drugs
containing Echinacea, symptoms like skin irritation, itching, facial
swelling, shortness of breath, dizziness, drop in blood pressure are
known.

Contraindications: This preparation should not be administered if cases of hypersensitivity


to any of the ingredients, exipients or compositae are known.
Furthermore, it should not be administered in patients with alcohol
problems or because of the ingredient Echinacea with progressive
systemic diseases such as tuberculosis, leucosis, inflammatory diseases
of the connective tissue (collagenosis), autoimmune diseases, multiple
sclerosis, AIDS, HIV infections and other chronic viral illnesses.

207
Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains 27.1 % (v/v) alcohol (ethanol).


Due to the alcohol content, professional medical advice should be
sought prior to recommending this product to patients with alcohol or
liver problems.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 30 ml and 100 ml dropper
bottle 3X/2X/4X, 2 ml ampule 10 and 50 3X/4X/4X.

208
Ruberkehl 3X
Suppositories
for rectal application

Active ingredient: Aspergillus ruber e volumine cellulae (lyophil., steril.) 3X

Composition: 1 suppository contains: Medically active substance: 0.2 g Aspergillus


ruber e volumine cellulae (lyophil., steril.) 3X trit. Other
constituents: hard fat, lactose.

According to experience, All chronic diseases of the upper and lower respiratory tract, such as
to be administered in rhinitis, sinusitis, bronchitis, conjunctivitis (red, itching eyes); cystitis
cases of: nephritis.

Characteristics: Observational studies with Ruberkehl, a homeopathic preparation


from Aspergillus ruber, have shown significant improvements in all
relevant symptoms of acute allergic rhinitis.

Application: Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally.


Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Ruberkehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Aspergillus ruber).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Ruberkehl .


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X.

209
Ruberkehl 5X
Ampules
Liquid dilution for injection

Active ingredient: Aspergillus ruber e volumine cellulae (lyophil., steril.) 5X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Aspergillus


ruber e volumine cellulae (lyophil., steril.) 5X aquous dil. Other
constituents: isotonic sodium chloride solution.

According to experience, All chronic diseases of the upper and lower respiratory tract, such as
to be administered in rhinitis, sinusitis, bronchitis, conjunctivitis (red, itching eyes); cystitis,
cases of: nephritis.

Characteristics: Observational studies with Ruberkehl, a homeopathic preparation


from Aspergillus ruber, have shown significant improvements in all
relevant symptoms of acute allergic rhinitis.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3x
weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Ruberkehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Aspergillus ruber).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Ruberkehl .


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

210
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X.

211
Ruberkehl 5X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Aspergillus ruber e volumine cellulae (lyophil., steril.) 5X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Asper-


gillus ruber e volumine cellulae (lyophil., steril.) 5X dil. Other
constituents: purified water.

According to experience, All chronic diseases of the upper and lower respiratory tract, such as
to be administered in rhinitis, sinusitis, bronchitis, conjunctivitis (red, itching eyes); cystitis,
cases of: nephritis.

Characteristics: Observational studies with Ruberkehl, a homeopathic preparation


from Aspergillus ruber, have shown significant improvements in all
relevant symptoms of acute allergic rhinitis.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Ruberkehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Aspergillus ruber).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Ruberkehl .


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: After opening, contents must be used within two months.

212
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 3X.

213
Sankombi 5X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredients: Mucor racemosus e volumine cellulae (lyophil., steril.) 5X,


Aspergillus niger e volumine cellulae (lyophil., steril.) 5X

Composition: 10 ml liquid dilution contain: Medically active substance: 5 ml Mucor


racemosus e volumine cellulae (lyophil., steril.) 5X dil., 5 ml
Aspergillus niger e volumine cellulae (lyophil., steril.) 5X dil.
Other constituents: purified water.

According to experience, Diseases due to circulatory disorders, such as embolism, thromboses,


to be administered in hemorrhoids; diseases related to a tuberculinic constitution, such as
cases of: degenerative or inflammatory conditions (Bechterews disease etc.),
lymphatism.

Characteristics: Sankombi 5X is a combination preparation that consists of equal


parts of Mucokehl 5X and Nigersan 5X. Mucokehl is produced
from the mold fungus Mucor racemosus Fresen. It has an influence
on all disorders of the blood and circulatory system and resulting
diseases. Nigersan is produced from the mold fungus Aspergillus
niger. It is a specifically acting preparation for isopathic treatment of
tuberculinic constitution and resulting diseases.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sankombi, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Mucor racemosus/ Aspergillus niger).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sankombi


with other remedies: 5X. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

214
Advice: After opening, contents must be used within two months.

Additional advice: In isopathic therapy, Sankombi is employed in the treatment of all


chronic diseases based on a disturbed endobiosis. This can be caused
by congestion as well as tuberculinic constitution.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage form is available: 10 ml dropper bottle 5X.

215
Sanoryzae 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Aspergillus oryzae e volumine cellulae (lyophil., steril.) 6X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Aspergillus oryzae e volumine cellulae (lyophil., steril.) 6X dil.
Other constituents: purified water.

According to experience, Coronary heart diseases, angina pectoris; migraine due to circulatory
to be administered in disorders; possibly hypertonia.
cases of:

Characteristics: Sanoryzae mainly acts on the vascular system by stimulating blood


circulation. The remedy rapidly develops its effectiveness particularly
in cases of circulatory disturbances in the coronary arteries, the inner
ear, as well as headaches resulting from disturbed circulation. Due to its
circulatory regulation properties, Sanoryzae can be administered for
treatment of high blood pressure.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanoryzae, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Aspergillus oryzae).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanoryzae.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

216
Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage form is available: 10 ml dropper bottle 6X.

217
Sanukehl Acne 5X
Ampules
Liquid dilution for injection

Active ingredient: Propionibacterium acnes extractum (lyophil., steril.) 5X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Propioni-


bacterium acnes extractum (lyophil., steril.) X aqueous dil.
Other constituents: isotonic sodium chloride solution.

According to experience, Acne conglobata; rheumatoid arthritis; venous and cerebral circulatory
to be administered in disorders.
cases of:

Characteristics: Sanukehl Acne contains specific extracts of polysaccharide com-


ponents (haptens) of Propionibacterium acnes. The effect is based
on the absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly or subcutaneously, 1-3 x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Acne, theo-


retically, hypersensitivity may occur, mainly in the form of skin reactions.
Also allergic reactions against the ingredient Propionibacterium
acnes are possible. In this case, discontinue medication and treat
symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Propioni-


bacterium species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Acne. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: None.

218
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.

219
Sanukehl Acne 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Propionibacterium acnes extractum (lyophil., steril.) 6X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Propionibacterium acnes extractum (lyophil., steril.) 6X dil.
Other constituents: purified water.

According to experience, Acne conglobata; rheumatoid arthritis; venous and cerebral circulatory
to be administered in disorders.
cases of:

Characteristics: Sanukehl Acne contains specific extracts of polysaccharide com-


ponents (haptens) of Propionibacterium acnes. The effect is based
on the absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: For oral intake: 1-2 x daily 5-10 drops. For
rubbing in: 1-2 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Acne, theo-


retically, hypersensitivity may occur, mainly in the form of skin reactions.
Also allergic reactions against the ingredient Propionibacterium
acnes are possible. In this case, discontinue medication and treat
symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Propioni-


bacterium species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Acne. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

220
Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.

221
Sanukehl Brucel 6X
Ampules
Liquid dilution for injection

Active ingredient: Brucella melitensis extractum (lyophil., steril.) 6X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Brucella


melitensis extractum (lyophil., steril.) 6X aquous dil. Other
constituents: isotonic sodium chloride solution.

According to experience, Myalgia, subacute polyarthritis; intermittent fever with influenza symptoms;
to be administered in neurasthenia; orchitis, epididymitis; headaches/migraine; lumbar syn-
cases of: drome.

Characteristics: Sanukehl Brucel contains specific extracts of polysaccharide


components (haptens) of Brucella melitensis. The effect is based on
the absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intra-


muscularly or subcutaneously, 1-3 x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Brucel, theo-


retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Brucella
melitensis are possible. In this case, discontinue medication and treat
symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Brucella


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Brucel. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

222
Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.

223
Sanukehl Brucel 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Brucella melitensis extractum (lyophil., steril.) 6X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Brucella


melitensis extractum (lyophil., steril.) 6X dil. Other constituents:
purified water.

According to experience, Myalgia, subacute polyarthritis; intermittent fever with influenza symptoms;
to be administered in neurasthenia; orchitis, epididymitis; headaches/migraine; lumbar syn-
cases of: drome.

Characteristics: Sanukehl Brucel contains specific extracts of polysaccharide


components (haptens) of Brucella melitensis. The effect is based on
the absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: For oral intake: 1-2 x daily 5-10 drops. For
rubbing in: 1-2 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Brucel, theo-


retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Brucella
melitensis are possible. In this case, discontinue medication and treat
symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Brucella


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Brucel. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

224
Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.

225
Sanukehl Cand 5X
Ampules
Liquid dilution for injection

Active ingredient: Candida albicans extractum Sero A et B (lyophil., steril.) 5X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Candida


albicans extractum Sero A et B (lyophil., steril.) 5X aquous dil.
Other constituents: isotonic sodium chloride solution.

According to experience, Diseases of the mouth, like stomatitis, gingivitis, perlche, aphthae;
to be administered in intestinal dysbiosis, candida infections, colitis, obstipation after treat-
cases of: ment with antibiotics; allergic asthma; vulvitis, vulvovaginitis, kraurosis
vulvae; dermatosis, e.g. after treatment with antibiotics.

Characteristics: Sanukehl Cand contains specific extracts of polysaccharide com-


ponents (haptens) of Candida albicans. The effect is based on the
absorption of the bacterial antigens and their toxins.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly or subcutaneously, 1-3 x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Cand, theo-


retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Candida
albicans are possible. In this case, discontinue medication and treat
symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Candida


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Cand. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

226
Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.

227
Sanukehl Cand 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Candida albicans extractum Sero A et B (lyophil., steril.) 6X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Candida


albicans extractum Sero A et B (lyophil., steril.) 6X dil. Other
constituents: purified water.

According to experience, Diseases of the mouth, like stomatitis, gingivitis, perlche, aphthae;
to be administered in intestinal dysbiosis, candida infections, colitis, obstipation after treat-
cases of: ment with antibiotics; allergic asthma; vulvitis, vulvovaginitis, kraurosis
vulvae; dermatosis, e.g. after treatment with antibiotics.

Characteristics: Sanukehl Cand contains specific extracts of polysaccharide


components (haptens) of Candida albicans. The effect is based on
the absorption of the bacterial antigens and their toxins.

Application: Unless otherwise prescribed: For oral intake: 1-2 x daily 5-10 drops. For
rubbing in: 1-2 x daily 5-10 into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Cand, theo-


retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Candida
albicans are possible. In this case, discontinue medication and treat
symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Candida


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Cand. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

228
Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.

229
Sanukehl Coli 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Escherichia coli extractum (lyophil., steril.) 6X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Esche-


richia coli extractum (lyophil., steril.) 6X dil. Other constituents:
purified water.

According to experience, Cholangitis, cholecystitis, gastroenteritis, colitis; pyelonephritis, cystitis;


to be administered in epididymitis, prostatitis; salpingitis, metritis, vaginitis; bronchitis.
cases of:

Characteristics: Sanukehl Coli contains specific extracts of polysaccharide com-


ponents (haptens) of Escherichia coli. The effect is based on the
absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: For oral intake: 1-2 x daily 5-10 drops. For
rubbing in: 1-2 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Coli, theo-


retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Escherichia
coli are possible. In this case, discontinue medication and treat
symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Escherichia


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Coli. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

230
Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 7X.

231
Sanukehl Coli 7X
Ampules
Liquid dilution for injection

Active ingredient: Escherichia coli extractum (lyophil., steril.) 7X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Escherichia


coli extractum (lyophil., steril.) 7X aquous dil. Other constituents:
isotonic sodium chloride solution.

According to experience, Cholangitis, cholecystitis, gastroenteritis, colitis; pyelonephritis, cystitis;


to be administered in epididymitis, prostatitis; salpingitis, metritis, vaginitis; bronchitis.
cases of:

Characteristics: Sanukehl Coli contains specific extracts of polysaccharide com-


ponents (haptens) of Escherichia coli. The effect is based on the
absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly or subcutaneously, 1-3 x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Coli, theo-


retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Escherichia
coli are possible. In this case, discontinue medication and treat
symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Escherichia


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Coli. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: None.

232
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 7X.

233
Sanukehl Klebs 6X
Ampules
Liquid dilution for injection

Active ingredient: Klebsiella pneumoniae extractum (lyophil., steril.) 6X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Klebsiella


pneumoniae extractum (lyophil., steril.) 6X aquous dil. Other
constituents: isotonic sodium chloride solution.

According to experience, Respiratory diseases; dysbiosis after antibiotic therapy.


to be administered in
cases of:

Characteristics: Sanukehl Klebs contains specific extracts of polysaccharide com-


ponents (haptens) of Klebsiella pneumoniae. The effect is based on
the absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly or subcutaneously, 1-3 x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Klebs, theo-


retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Klebsiella
pneumoniae are possible. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Klebsiella


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Klebs. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: After opening, contents must be used within two months.

234
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.

235
Sanukehl Klebs 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Klebsiella pneumoniae extractum (lyophil., steril.) 6X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Klebsiella pneumoniae extractum (lyophil., steril.) 6X dil. Other
constituents: purified water.

According to experience, Respiratory diseases; dysbiosis after antibiotic therapy.


to be administered in
cases of:

Characteristics: Sanukehl Klebs contains specific extracts of polysaccharide


components (haptens) of Klebsiella pneumonia. The effect is based on
the absorption of the bacterial antigens and their toxins.

Application: Unless otherwise prescribed: For oral intake: 1-2 x daily 5-10 drops. For
rubbing in: 1-2 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Klebs, theo-


retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Klebsiella
pneumoniae are possible. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Klebsiella


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Klebs. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

236
Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.

237
Sanukehl Myc 5X
Ampules
Liquid dilution for injection

Active ingredient: Mycobacterium bovis (BCG) extractum (lyophil., steril.) 5X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Myco-


bacterium bovis (BCG) extractum (lyophil., steril.) 5X aquous
dil. Other constituents: isotonic sodium chloride solution.

According to experience, Respiratory diseases, such as bronchial asthma, pleurisy, rhinitis;


to be administered in chronic recurrent diseases of the skin and the mucous membranes,
cases of: such as juvenile acne, urticaria, hordeolum, psoriasis; lupus erythema-
tosus; arthritis; osteochondrosis; cholecystitis; enterocolitis; ventricular
and duodenal ulcer; headache; metritis; nephritis; otitis.

Characteristics: Sanukehl Myc contains specific extracts of polysaccharide com-


ponents (haptens) of Mycobacterium bovis (BCG). The effect is
based on the absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly or subcutaneously, 1-3 x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Myc, theo-


retically, hypersensitivity may occur, mainly in the form of skin reactions.
Also allergic reactions against the ingredient Mycobacterium bovis
(BCG) are possible. In this case, discontinue medication and treat
symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Mycobacterium


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Myc. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

238
Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.

239
Sanukehl Myc 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Mycobacterium bovis (BCG) extractum (lyophil., steril.) 6X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Mycobacterium bovis (BCG) extractum (lyophil., steril.) 6X dil.
Other constituents: purified water.

According to experience, Respiratory diseases, such as bronchial asthma, pleurisy, rhinitis chronic;
to be administered in recurrent diseases of the skin and the mucous membranes, such as
cases of: juvenile acne, urticaria, hordeolum, psoriasis; lupus erythematosus;
arthritis; osteochondrosis; cholecystitis; enterocolitis; ventricular and
duodenal ulcer; headache; metritis; nephritis; otitis.

Characteristics: Sanukehl Myc contains specific extracts of polysaccharide com-


ponents (haptens) of Mycobacterium bovis (BCG). The effect is
based on the absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: For oral intake: 1-2 x daily 5-10 drops. For
rubbing in: 1-2 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Myc, theo-


retically, hypersensitivity may occur, mainly in the form of skin reactions.
Also allergic reactions against the ingredient Mycobacterium bovis
(BCG) are possible. In this case, discontinue medication and treat
symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Mycobacterium


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Myc. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

240
Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.

241
Sanukehl Prot 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Proteus vulgaris extractum (lyophil., steril.) 6X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Proteus


vulgaris extractum (lyophil., steril.) 6X dil. Other constituents:
purified water.

According to experience, Otitis; osteomyelitis; intestinal dysbiosis after treatment with antibiotics;
to be administered in ulcerative colitis; angina; rheumatic disorders; chronic suppurative
cases of: affections of the respiratory and intestinal tract.

Characteristics: Sanukehl Prot contains specific extracts of polysaccharide com-


ponents (haptens) of Proteus vulgaris. The effect is based on the
absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: For oral intake: 1-2 x daily 5-10 drops. For
rubbing in: 1-2 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Prot, theo-


retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Proteus
vulgaris are possible. In this case, discontinue medication and treat
symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Proteus


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Prot. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: After opening, contents must be used within two months.

242
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 7X.

243
Sanukehl Prot 7X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Proteus vulgaris extractum (lyophil., steril.) 7X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Proteus


vulgaris extractum (lyophil., steril.) 7X aquous dil. Other
constituents: isotonic sodium chloride solution.

According to experience, Otitis; osteomyelitis; intestinal dysbiosis after treatment with antibiotics;
to be administered in ulcerative colitis; angina; rheumatic disorders; chronic suppurative
cases of: affections of the respiratory and intestinal tract.

Characteristics: Sanukehl Prot contains specific extracts of polysaccharide com-


ponents (haptens) of Proteus vulgaris. The effect is based on the
absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intra-


muscularly or subcutaneously, 1-3 x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Prot, theo-


retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Proteus
vulgaris are possible. In this case, discontinue medication and treat
symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Proteus species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Prot. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: None.

244
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 7X.

245
Sanukehl Pseu 6X
Ampules
Liquid dilution for injection

Active ingredient: Pseudomonas aeruginosa extractum (lyophil., steril.) 6X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Pseu-


domonas aeruginosa extractum (lyophil., steril.) 6X aquous dil.
Other constituents: isotonic sodium chloride solution.

According to experience, Respiratory disorders, such as bronchial asthma; otitis; sinusitis; pharyngitis,
to be administered in hay fever, chronic bronchitis; infectious and infectious and allergic
cases of: dermatitis, pruritus, collagenosis, fibromyalgia, ulcer cruris, keloids,
burns, autoimmune diseases, treatment of complaints caused by
immunosuppressive treatment.

Characteristics: Sanukehl Pseu contains specific extracts of polysaccharide com-


ponents (haptens) of Pseudomonas aeruginosa. The effect is based
on the absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intra-


muscularly or subcutaneously, 1-3 x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Pseu, theo-


retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Pseudomonas
aeruginosa are possible. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Pseudomonas


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Pseu. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

246
Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.

247
Sanukehl Pseu 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Pseudomonas aeruginosa extractum (lyophil., steril.) 6X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Pseu-


domonas aeruginosa extractum (lyophil., steril.) 6X dil. Other
constituents: purified water.

According to experience, Respiratory disorders, such as bronchial asthma; otitis; sinusitis; pharyn-
to be administered in gitis, hay fever, chronic bronchitis; infectious and infectious and
cases of: allergic dermatitis, pruritus, collagenosis, fibromyalgia, ulcer cruris,
keloids, burns, autoimmune diseases, treatment of complaints caused
by immunosuppressive treatment.

Characteristics: Sanukehl Pseu contains specific extracts of polysaccharide com-


ponents (haptens) of Pseudomonas aeruginosa. The effect is based
on the absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: For oral intake: 1-2 x daily 5-10 drops. For
rubbing in: 1-2 x daily 5-10 drops into the bend of the elbow.

Treatment of more than 8 weeks depends on the advice of the physician


or health care professional.

Side effects: Because of specific organic components of Sanukehl Pseu, theo-


retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Pseudomonas
aeruginosa are possible. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Pseudomonas


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Pseu 6X. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

248
Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.

249
Sanukehl Salm 6X
Ampules
Liquid dilution for injection

Active ingredient: Salmonella enteritidis extractum (lyophil., steril.) 6X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Salmonella


enteritidis extractum (lyophil., steril.) 6X aquous dil. Other
constituents: isotonic sodium chloride solution.

According to experience, Impaired development; chronic pancreatitis, chronic gastroenteritis;


to be administered in celiac disease; rheumatic fever.
cases of:

Characteristics: Sanukehl Salm contains specific extracts of polysaccharide com-


ponents (haptens) of Salmonella enteritidis. The effect is based on
the absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly or subcutaneously, 1-3 x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Salm, theo-


retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Salmonella
enteritidis are possible. In this case, discontinue medication and treat
symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Salmonella


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Salm. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: None.

250
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.

251
Sanukehl Salm 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Salmonella enteritidis extractum (lyophil., steril.) 6X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Salmonella enteritidis extractum (lyophil., steril.) 6X dil. Other
constituents: purified water.

According to experience, Impaired development; chronic pancreatitis, chronic gastroenteritis;


to be administered in celiac disease; rheumatic fever.
cases of:

Characteristics: Sanukehl Salm contains specific extracts of polysaccharide com-


ponents (haptens) of Salmonella enteritidis. The effect is based on
the absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: For oral intake: 1-2 x daily 5-10 drops. For
rubbing in: 1-2 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Salm, theo-


retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Salmonella
enteritidis are possible. In this case, discontinue medication and treat
symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Salmonella


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Salm. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

252
Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 6X.

253
Sanukehl Serra 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Serratia marcescens extractum (lyophil., steril.) 6X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Serratia marcescens extractum (lyophil., steril.) 6X dil. Other
constituents: purified water.

According to experience, Nosocomial infections with Serratia marcescens.


to be administered in
cases of:

Characteristics: Sanukehl Serratia contains specific extracts of polysaccharide


components (haptens) of Serratia marcescens. The effect is based
on the absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: For oral intake: 1-2 x daily 5-10 drops. For
rubbing in: 1-2 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Serra, theo-


retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Serratia
marcescens are possible. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Serratia


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Serra. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

254
Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 7X.

255
Sanukehl Serra 7X
Ampules
Liquid dilution for injection

Active ingredient: Serratia marcescens extractum (lyophil., steril.) 7X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Serratia


marcescens extractum (lyophil., steril.) 7X aquous dil. Other
constituents: isotonic sodium chloride solution.

According to experience, Nosocomial infections with Serratia marcescens.


to be administered in
cases of:

Characteristics: Sanukehl Serratia contains specific extracts of polysaccharide


components (haptens) of Serratia marcescens. The effect is based
on the absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly or subcutaneously, 1-3 x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Serra,


theoretically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Serratia
marcescens are possible. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Serratia


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Serra. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: None.

256
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 7X.

257
Sanukehl Staph 5X
Ampules
Liquid dilution for injection

Active ingredient: Staphylococcus aureus extractum (lyophil., steril.) 5X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Staphy-


lococcus aureus extractum (lyophil., steril.) 5X aquous dil. Other
constituents: isotonic sodium chloride solution.

According to experience, Folliculosis, furunculosis, impetigo, acne conglobata; blepharitis, hor-


to be administered in deolum, chalazion, angina, otitis, mastoiditis, sinusitis; meningitis;
cases of: osteomyelitis; nephritis, urogenital infections with staphylococci.

Characteristics: Sanukehl Staph contains specific extracts of polysaccharide com-


ponents (haptens) of Staphylococcus aureus. The effect is based on
the absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly or subcutaneously, 1-3 x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Staph, theo-


retically, hypersensitivity may occur, mainly in the form of skin reactions.
Also allergic reactions against the ingredient Staphylococcus
aureus are possible. In this case, discontinue medication and treat
symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Staphylococcus


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Staph. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

258
Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.

259
Sanukehl Staph 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Staphylococcus aureus extractum (lyophil., steril.) 6X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Staphylococcus aureus extractum (lyophil., steril.) 6X dil.
Other constituents: purified water.

According to experience, Folliculosis, furunculosis, impetigo, acne conglobata; blepharitis,


to be administered in hordeolum, chalazion, angina, otitis, mastoiditis, sinusitis; meningitis;
cases of: osteomyelitis; nephritis, urogenital infections with staphylococci.

Characteristics: Sanukehl Staph contains specific extracts of polysaccharide com-


ponents (haptens) of Staphylococcus aureus. The effect is based on
the absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: For oral intake: 1-2 x daily 5-10 drops. For
rubbing in: 1-2 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Staph, theo-


retically, hypersensitivity may occur, mainly in the form of skin reactions.
Also allergic reactions against the ingredient Staphylococcus
aureus are possible. In this case, discontinue medication and treat
symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Staphylococcus


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Staph. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: After opening, contents must be used within two months.

260
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.

261
Sanukehl Strep 5X
Ampules
Liquid dilution for injection

Active ingredient: Streptococcus pyogenes extractum (lyophil., steril.) 5X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Strepto-


coccus pyogenes extractum (lyophil., steril.) 5X aquous dil.
Other constituents: isotonic sodium chloride solution.

According to experience, Angina tonsillaris; eczema; endo-, myo- and pericarditis; empyema;
to be administered in mastitis puerperalis; osteomyelitis; otitis media; sinubronchitis; phleg-
cases of: mons; primary chronic polyarthritis.

Characteristics: Sanukehl Strep contains specific extracts of polysaccharide com-


ponents (haptens) of Streptococcus pyogenes. The effect is based
on the absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly or subcutaneously, 1-3 x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Strep, theo-


retically, hypersensitivity may occur, mainly in the form of skin reactions.
Also allergic reactions against the ingredient Streptococcus
pyogenes are possible. In this case, discontinue medication and treat
symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Streptococcus


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Strep. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: None.

262
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.

263
Sanukehl Strep 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Streptococcus pyogenes extractum (lyophil., steril.) 6X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml Strep-


tococcus pyogenes extractum (lyophil., steril.) 6X dil. Other
constituents: purified water.

According to experience, Angina tonsillaris; eczema; endo-, myo- and pericarditis; empyema;
to be administered in mastitis puerperalis; osteomyelitis; otitis media; sinubronchitis; phleg-
cases of: mons; primary chronic polyarthritis.

Characteristics: Sanukehl Strep contains specific extracts of polysaccharide com-


ponents (haptens) of Streptococcus pyogenes. The effect is based
on the absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: For oral intake: 1-2 x daily 5-10 drops. For
rubbing in: 1-2 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Strep, theo-


retically, hypersensitivity may occur, mainly in the form of skin reactions.
Also allergic reactions against the ingredient Streptococcus
pyogenes are possible. In this case, discontinue medication and treat
symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Streptococcus


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Strep. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

264
Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.

265
Sanukehl Trich 5X
Ampules
Liquid dilution for injection

Active ingredient: Trichophyton verrucosum extractum (lyophil., steril.) 5X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Tricho-


phyton verrucosum extractum (lyophil., steril.) 5X aquous dil.
Other constituents: isotonic sodium chloride solution.

According to experience, Mycosis of the hair, skin, nails, tinea, trichophytosis; impairment of skin
to be administered in function; hair loss.
cases of:

Characteristics: Sanukehl Trich contains specific extracts of polysaccharide com-


ponents (haptens) of Trichophyton verrucosum. The effect is based
on the absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly or subcutaneously, 1-3 x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Trich, theo-


retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Trichophyton
verrucosum are possible. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Trichophyton


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Trich. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: None.

266
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.

267
Sanukehl Trich 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Trichophyton verrucosum extractum (lyophil., steril.) 6X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Trichophyton verrucosum extractum (lyophil., steril.) 6X dil.
Other constituents: purified water.

According to experience, Mycosis of the hair, skin, nails, tinea, trichophytosis; impairment of
to be administered in skin function; hair loss.
cases of:

Characteristics: Sanukehl Trich contains specific extracts of polysaccharide com-


ponents (haptens) of Trichophyton verrucosum. The effect is based
on the absorption of the pathogens antigens and toxins.

Application: Unless otherwise prescribed: For oral intake: 1-2 x daily 5-10 drops. For
rubbing in: 1-2 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Sanukehl Trich, theo-


retically, hypersensitivity may occur, mainly in the form of skin
reactions. Also allergic reactions against the ingredient Trichophyton
verrucosum are possible. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Trichophyton


species.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Sanukehl


with other remedies: Trich. An interval of 4 weeks before and after treatment with orally
administered live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

268
Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml
ampule 10 and 50 5X.

269
Sanumgerman 6X
Drops
Liquid dilution for oral intake

Active ingredient: Di-potassium-germanium(IV)-citrate-L(+)lactate 6X

Composition: 100 ml liquid dilution contain: Medically active substance: 100 ml


Di-potassium-germanium(IV)-citrate-L(+)lactate 6X dil. Other
constituents: purified water, ethanol.

According to experience, Peripheral arterial circulatory disorders, cerebrosclerosis, Raynauds


to be administered in disease; chronic rheumatism; Parkinsons disease; epilepsy; adjuvant
cases of: therapy for cancer.

Characteristics: Sanumgerman is an organic compound of germanium that positively


influences growth and regulation of biological systems in vitro and
in vivo. In the periodic system of the chemical elements, germanium
belongs to the same main group as silicon, which explains its regulative
ability. Experimental examinations have shown that germanium
protects against oxidation of enzymes with SH-groups, resulting in
an improvement of the defense against free radicals and peroxides.
Because of its immunmodulatoric effect, organic germanium supports
the formation of interferons as well as the activation of macrophages
and natural killer cells. In animal experiments, its sedative effects on the
central nervous system were also established.

Application: Unless otherwise prescribed: For oral intake: 1-3 x daily 10 drops before
a meal.

Side effects: None known.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains 12.4 % (v/v) alcohol (ethanol).


Due to the alcohol content, professional medical advice should be
sought prior to recommending this product to patients with alcohol or
liver problems.

270
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage form is available: 100 ml dropper bottle 6X.

271
Sanuvis 1X
Ointment
for rubbing in

Active ingredient: Acidum lacticum 1X

Composition: 1 g ointment contains: Medically active substance: 0.1 g Acidum


lacticum 1X dil. Other constituents: 0.38 g lanolin alcohol ointment,
0.10 g coconut oil fract., 0.03 g glyceryl monostearate 40-55%, 0.23
g propylene glycol, 0.02 g magnesium sulphate x 7 H2O, 0.01 g lactic
acid, 0.14 g water for injection.

According to experience, Regulation of the pH value, especially for chronic skin diseases like
to be administered in psoriasis, ichthyosis, rhagades.
cases of:

Characteristics: Sanuvis contains Acidum lacticum (lactic acid) which affects meta-
bolic processes.

Application: Unless otherwise prescribed: Apply thinly on the affected area 1 to 3 x


daily.

Side effects: None known.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 30 ml dropper bottle 2X, 100
ml dropper bottle 4X/6X/12X/30X/200X potency mixture, 2 ml ampule
10 and 50 4X/6X/12X/30X/200X potency mixture, 80 tablets 4X/6X/12X/
30X/200X potency mixture, 30 g tube of ointment 1X.

272
Sanuvis 2X
Drops
Liquid dilution for oral intake

Active ingredient: Acidum lacticum 2X

Composition: 1 ml liquid dilution contains: Medically active substance: 1 ml Acidum


lacticum 2X dil. Other constituents: purified water, ethanol.

According to experience, Disorders of the acid alkaline balance, metabolic disturbances mainly
to be administered in resulting from the increased production of levorotatory lactic acid e.g.
cases of: diabetes, tissue degeneration and functional heart disorders; skin
diseases such as psoriasis and ichthyosis.

Characteristics: Sanuvis contains Acidum lacticum (lactic acid) which affects


metabolic processes.

Application: Unless otherwise prescribed: For oral intake: 1-3 x daily 5 drops.

Side effects: None known.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains 19 % (v/v) alcohol (ethanol).


Due to the alcohol content, professional medical advice should be
sought prior to recommending this product to patients with alcohol or
liver problems.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 30 ml dropper bottle 2X, 100
ml dropper bottle 4X/6X/12X/30X/200X potency mixture, 2 ml ampule
10 and 50 4X/6X/12X/30X/200X potency mixture, 80 tablets 4X/6X/12X/
30X/200X potency mixture, 30 g tube of ointment 1X.

273
Sanuvis
Ampules
Liquid dilution for injection

Active ingredient: Acidum lacticum 4X/6X/12X/30X/200X

Composition: 1 ampule of 2 ml contains: Medically active substance: 0.4 ml Acidum


lacticum 4X aquous dil., 0.4 ml Acidum lacticum 6X aquous dil.,
0.4 ml Acidum lacticum 12X aquous dil., 0.4 ml Acidum lacticum
30X aquous dil., 0.4 ml Acidum lacticum 200X aquous dil. Other
constituents: isotonic sodium chloride solution.

According to experience, Disorders of the acid alkaline balance and of intermediary metabolism;
to be administered in chronic skin diseases and circulatory disorders.
cases of:

Characteristics: Sanuvis contains a mixes potency of Acidum lacticum (lactic acid)


which affects metabolic processes. Sanuvis can be administered
as a basic remedy in addition to the fungal preparations. In Isopathy,
Sanuvis is applied as an adjuvant to Mucokehl.

Application: Unless otherwise prescribed: 1 ampule of 2 ml to be injected intramus-


cularly, 1-3 x weekly.

Side effects: None known.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 30 ml dropper bottle 2X, 100
ml dropper bottle 4X/6X/12X/30X/200X potency mixture, 2 ml ampule
10 and 50 4X/6X/12X/30X/200X potency mixture, 80 tablets 4X/6X/12X/
30X/200X potency mixture, 30 g tube of ointment 1X.

274
Sanuvis
Drops
Liquid dilution for oral intake

Active ingredient: Acidum lacticum 4X/6X/12X/30X/200X

Composition: 100 ml liquid dilution contains: Medically active substance: 20 ml


Acidum lacticum 4X dil., 20 ml Acidum lacticum 6X dil., 20 ml
Acidum lacticum 12X dil., 20 ml Acidum lacticum 30X dil., 20
ml Acidum lacticum 200X dil. Other constituents: purified water,
ethanol.

According to experience, Disorders of the acid alkaline balance and of intermediary metabolism;
to be administered in chronic skin diseases and circulatory disorders.
cases of:

Characteristics: Sanuvis contains a mixes potency of Acidum lacticum (lactic acid)


which affects metabolic processes. Sanuvis can be administered
as a basic remedy in addition to the fungal preparations. In Isopathy,
Sanuvis is applied as an adjuvant to Mucokehl.

Application: Unless otherwise prescribed: For oral intake: 1-3 x daily 5-20 drops.

Side effects: None known.

Contraindications: This product contains 36.2 % (v/v) alcohol (ethanol). This may present
a health risk in cases of liver diseases, alcoholism, epilepsy, brain
damage, pregnancy, and in children. The action of other drugs may be
reduced or intensified.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains 36.2 % (v/v) alcohol (ethanol).

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 30 ml dropper bottle 2X, 100
ml dropper bottle 4X/6X/12X/30X/200X potency mixture, 2 ml ampule
10 and 50 4X/6X/12X/30X/200X potency mixture, 80 tablets 4X/6X/12X/
30X/200X potency mixture, 30 g tube of ointment 1X.

275
Sanuvis
Tablets
for oral intake

Active ingredient: Acidum lacticum 4X/6X/12X/30X/200X

Composition: 1 tablet contains: Medically active substance: 50 mg Acidum lacticum


4X trit., 50 mg Acidum lacticum 6X trit., 50 mg Acidum lacticum
12X trit., 50 mg Acidum lacticum 30X trit., 50 mg Acidum lacticum
200X trit. Other constituents: lactose, potato starch, magnesium
stearate.

According to experience, Disorders of the acid alkaline balance and of intermediary metabolism;
to be administered in chronic skin diseases and circulatory disorders.
cases of:

Characteristics: Sanuvis contains a mixes potency of Acidum lacticum (lactic acid)


which affects metabolic processes. Sanuvis can be administered
as a basic remedy in addition to the fungal preparations. In Isopathy,
Sanuvis is applied as an adjuvant to Mucokehl.

Application: Unless otherwise prescribed: 1-3 x daily 1-2 tablets.

Side effects: None known.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 30 ml dropper bottle 2X, 100
ml dropper bottle 4X/6X/12X/30X/200X potency mixture, 2 ml ampule
10 and 50 4X/6X/12X/30X/200X potency mixture, 80 tablets 4X/6X/12X/
30X/200X potency mixture, 30 g tube of ointment 1X.

276
Selenokehl 4X
Ampules
Liquid dilution for injection

Active ingredient: Natrium selenosum 4X

Composition: 1 ampule of 2 ml contains: Medically active substance: 0.16 ml


Natrium selenosum 4X aquous dil. Other constituents: isotonic
sodium chloride solution.

According to experience, Selenium deficiency due to malnutrition and malabsorption, for amal-
to be administered in gam detoxification.
cases of:

Characteristics: Selenium is an essential trace element. In the human body it is chiefly


connected with the enzyme glutathione peroxidase which is a constituent
of the antioxidative protective system of the cell. In test models it has
been proven that the selenium-containing glutathione peroxidase is one
of the bodys strongest, most effective enzymes for absorbing radicals.
Among other benefits, it lowers the rate of peroxidation of lipids and
thereby protects the cellular membrane from damages. Selenium
deficiency increases the toxicity of heavy metals such as mercury, lead
and cadmium, and also it potentizes weakness of the liver caused by
oxidative and chemical influences.

Application: Unless otherwise prescribed: 1 ampule of 2 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1-2
x daily.

Side effects: None known.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

277
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml and 30 ml dropper
bottle 4X, 2 ml ampule 10 and 50 4X.

278
Selenokehl 4X
Drops
Liquid dilution for oral intake

Active ingredient: Natrium selenosum 4X

Composition: 10 ml liquid dilution contain: Medically active substance: 0.8 ml Natrium


selenosum 4X dil. Other constituents: purified water, ethanol 15 %
(m/m).

According to experience, Selenium deficiency due to malnutrition and malabsorption, for amal-
to be administered in gam detoxification.
cases of:

Characteristics: Selenium is an essential trace element. In the human body it is chiefly


connected with the enzyme glutathione peroxidase which is a constituent
of the antioxidative protective system of the cell. In test models it has
been proven that the selenium-containing glutathione peroxidase is one
of the bodys strongest, most effective enzymes for absorbing radicals.
Among other benefits, it lowers the rate of peroxidation of lipids and
thereby protects the cellular membrane from damages. Selenium
deficiency increases the toxicity of heavy metals such as mercury, lead
and cadmium, and also it potentizes weakness of the liver caused by
oxidative and chemical influences.

Application: Unless otherwise prescribed: For oral intake: in case of acute conditions
every half to one hour not more than 6 times daily each 5 drops. In case
of chronic conditions 1-3 x daily 5 drops.

Side effects: None known.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains 20 % (v/v) alcohol (ethanol).


Due to the alcohol content, professional medical advice should be
sought prior to recommending this product to patients with alcohol or
liver problems.

279
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml and 30 ml dropper
bottle 4X, 2 ml ampule 10 and 50 4X.

280
Silvaysan
Capsules
for oral intake

Active ingredient: Milk-thistle dry extract, refined and standardised

Composition: 1 Capsule contains: 136 - 160 mg Milk-thistle dry extract, refined


and standardised (50-70:1) equivalent to 86,6 mg Silymarin, taken into
account for Silibinin (extractive substance: acetone). Standardisation
material: dextrose 0 to 24 mg. Other constituents: highly dispersed
silica, dextrose, lactose 1 H2O, magnesium stearate, gelatin, purified
water.

Indication: Supporting treatment of chronic inflammatory liver diseases and cirrhosis


of the liver as well as toxic liver damage.
This remedy is not intended for treatment of acute poisoning.

Characteristics: Silymarins therapeutic effects are based on two targets or modes of


action: Silymarin changes the structure of the outer cell membrane of
the hepatocytes in such a way that hepatotoxins cannot enter into the
cell. Silymarin stimulates the activity of the nucleolar polymerase A,
resulting in an increased ribosomal protein synthesis, thus stimulating
the regenerative power of the liver and the neogenesis of hepatocytes.

Application: Unless otherwise prescribed: 3 x daily 1 capsule.

Side effects: Occasionally, gastrointestinal complaints, such as nausea or a mild


laxative effect. In rare cases hypersensitivity reactions such as rash,
itching, breathing difficulties may occur. In this case, discontinue
medication and treat symptomatically.

Contraindications: This preparation should not be administered if cases of hypersensitivity


against milk-thistle and/or other compositae as well as any of the
ingredients are known.

Adverse reactions: None known.

Interactions The improvement of liver function under intake of Silvaysan influences


with other remedies: the metabolism of other concurrently taken drugs. Possibly, dosage
adjustments become necessary.
Simultaneous intake of Silvaysan and Amiodaron (drug for treatment
of cardiac arrhythmia) may lead to an increased antiarrhythmic effect of
Amiodaron.

281
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: The drug therapy does not replace the avoidance of the hepatotoxic
causes (e.g. alcohol). In case of icterus (light- to dark-yellow colored
skin, yellow colored sclera), professional medical advice should be
sought immediately. Silvaysan is not suitable for the treatment of
acute intoxication.
This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 20 and 100 capsules.

282
Stolonikehl 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Penicillium brevicompactum e volumine cellulae (lyophil., steril.) 6X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Penicillium brevicompactum e volumine cellulae (lyophil.,
steril.) 6X dil. Other constituents: purified water.

According to experience, Intercostal neuralgia; trigeminal neuralgia.


to be administered in
cases of:

Characteristics: Penicillium stoloniferum, an ubiquitous mold fungus, has proven its


worth for treatment of viral diseases.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Stolonikehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


(Penicillium brevicompactum).

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Stolonikehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage form is available: 10 ml dropper bottle 6X.

283
Strophantus 4X Sanum
Drops
Liquid dilution
for oral intake

Active ingredient: Strophantus gratus 4X dil.

Composition: 1 ml liquid dilution contains: Medically active substance: 1 ml


Strophanthus gratus 4X dil. Other constituents: purified water,
ethanol.

Indication: Cardiac weakness, increasing blood volume, hypertension; sodium


burden; nervous heart by reason of smoking; arteriosclerosis; cardiac
decompensation; anticipatory anxiety.

Characteristics: Strophanthin, also known as Ouabain, was used by the African


natives as arrow poison for a long time. It is produced from a milk-
secreting climbing plant, but it is also an endogenous hormone which
is produced in the adrenal gland and is involved in the regulation of salt
and water balance. The human hypophysis contains an isomer of g-
Strophanthin. Therefore, g-Strophanthin is an endogenic substance. By
its influence, myocardial activity can be relieved significantly. Weakness
of the adrenal gland which often occurs with increasing age, as well as
senile heart weakness can be balanced with G-Strophanthin.

Application: Unless otherwise prescribed:


For oral intake: in case of acute conditions 5 drops every half to full
hour up to a maximum of 12 times daily. In case of chronic conditions 5
drops up to 3 times daily.

Side effects: Because of the specific organic components of Strophantus 4X


Sanum, theoretically, hypersensitivity may occur. In this case,
discontinue use and treat symptomatically.

Contraindications: This product contains 51 % (v/v) alcohol (ethanol). Following the dosage
recommendations for acute conditions the alcohol intake amounts up
to 0.3g; following the dosage recommendations for chronic conditions
the alcohol intake amounts up to 0.15g. This may present a health
risk in cases of liver diseases, alcoholism, epilepsy, brain damage,
pregnancy, and in children. The action of other drugs may be reduced
or intensified.

Adverse reactions: None known.

Interactions
with other remedies: None known.

284
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children. This also applies to patients with renal insufficiency and
patients with heart failure.
Strophantus 4X Sanum should not be administered with other
preparations containing cardiac glycosides.

Advice: This product contains 51 % (v/v) alcohol (ethanol). Following the dosage
recommendations for acute conditions the alcohol intake amounts up
to 0.3g; following the dosage recommendations for chronic conditions
the alcohol intake amounts up to 0.15g. This may present a health
risk in cases of liver diseases, alcoholism, epilepsy, brain damage,
pregnancy, and in children. The action of other drugs may be reduced
or intensified.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml, 30ml, 100 ml dropper
bottle 4X, 80 tablets 4X.

285
Strophantus 4X Sanum
Tablets
for oral intake

Active ingredient: Strophantus gratus 4X

Composition: 1 tablet contains: Medically active substance: 250 mg Strophanthus


gratus 4X trit. Other constituents: lactose, potato starch, magnesium
stearate.

Indication: Cardiac weakness, increasing blood volume, hypertension; sodium


burden; nervous heart by reason of smoking; arteriosclerosis; cardiac
decompensation; anticipatory anxiety.

Characteristics: Strophanthin, also known as Ouabain, was used by the African


natives as arrow poison for a long time. It is produced from a milk-
secreting climbing plant, but it is also an endogenous hormone which
is produced in the adrenal gland and is involved in the regulation of salt
and water balance. The human hypophysis contains an isomer of g-
Strophanthin. Therefore, g-Strophanthin is an endogenic substance. By
its influence, myocardial activity can be relieved significantly. Weakness
of the adrenal gland which often occurs with increasing age, as well as
senile heart weakness can be balanced with G-Strophanthin.

Application: Unless otherwise prescribed:


For oral intake: in case of acute conditions 1 tablet every half to full
hour up to a maximum of 12 times daily. In case of chronic conditions 2
tablets daily.

Side effects: Because of the specific organic components of Strophantus 4X


Sanum, theoretically, hypersensitivity may occur. In this case,
discontinue use and treat symptomatically.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children. This also applies to patients with renal insufficiency and
patients with heart failure.
Strophantus 4X Sanum should not be administered with other
preparations containing cardiac glycosides.

286
Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml, 30ml, 100 ml dropper
bottle 4X, 80 tablets 4X.

287
Taraxan 3X
Ampules
Liquid dilution for injection

Active ingredient: Taraxacum officinale 3X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml


Taraxacum officinale 3X aquous dil. Other constituents: isotonic
sodium chloride solution.

According to experience, Blood and tissue cleansing; stimulation of digestive juices, especially
to be administered in bile flow; kidney support.
cases of:

Characteristics: Taraxacum officinale is rich in tannins and bitter substances,


especially taraxin, as well as inulin, fructose, minerals and trace
elements. Since the Middle Ages, various dandelion preparations were
used as food and as plant drugs for liver and kidney support, thus
enabling blood and tissue cleansing.
The following symptoms result from the homeopathic drug picture of
Taraxacum officinale: main effects on liver, bile and urine excretion;
strained muscles and joints of the entire body; venous congestions;
upper abdominal complaints; pruritus. Motion improves the symptoms;
resting, lying down and cold, wet weather worsen the complaints.
Taraxan 3X can be administered as accompanying remedy with
all therapies which make support of detoxification and excretion
necessary.

Application: Unless otherwise prescribed:


1 ampule of 1 ml to be injected either intramuscularly, subcutaneously,
intracutaneously or intravenously, 1 x daily.

Side effects: None known.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

288
Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 1 ml ampule 10 and 50 3X.

289
Thymokehl 6X
Ampules
Liquid dilution for injection

Active ingredient: Glandula thymi (lyophil., steril.) 6X

Composition: 1 ampule of 2 ml contains: Medically active substance: 2 ml Glandula


thymi (lyophil., steril.) 6X aquous dil. Other constituents: isotonic
sodium chloride solution.

According to experience, Disorders in growth and development; adjuvant in anti-carcinogenic


to be administered in therapy; for all degenerative processes in the lumbar vertebral column
cases of: area.

Characteristics: Extracts from organs act positively on the entire cell metabolism. In
cellular therapy, research has shown that materials resorbed from
organ extracts promote cellular repair processes of the DNA. They act
as a stimulant where damaged cells need to be regenerated and as a
supplement where degenerated cells break down. The thymus extract
in Thymokehl shows the same physiological activity; its molecular
structure differs only slightly from the molecular structure of the human
organ. The promotion of cellular respiration by the thymus extract has
been proven in various animal test models.

Application: Unless otherwise prescribed: 1 ampule of 2 ml to be injected either


intramuscularly, subcutaneously or intracutaneously, 1-3 x weekly.

Side effects: Because of specific organic components of Thymokehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,


especially calf protein.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

290
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 2 ml ampule 10 and 50 6X, 10
suppositories 6X, 20 capsules 6X.

291
Thymokehl 6X
Capsules
for oral intake

Active ingredient: Glandula thymi (lyophil., steril.) 6X

Composition: 1 capsule contains: Medically active substance: 330 mg Glandula


thymi (lyophil., steril.) 6X trit. Other constituents: lactose, hypro-
mellosis (capsule shell).

According to experience, Disorders in growth and development; adjuvant in anti-carcinogenic


to be administered in therapy; for all degenerative processes in the lumbar vertebral column
cases of: area.

Characteristics: Extracts from organs act positively on the entire cell metabolism. In
cellular therapy, research has shown that materials resorbed from
organ extracts promote cellular repair processes of the DNA. They act
as a stimulant where damaged cells need to be regenerated and as a
supplement where degenerated cells break down. The thymus extract
in Thymokehl shows the same physiological activity; its molecular
structure differs only slightly from the molecular structure of the human
organ. The promotion of cellular respiration by the thymus extract has
been proven in various animal test models.

Application: Unless otherwise prescribed: 1-3 x daily 1 capsule.

Side effects: Because of specific organic components of Thymokehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,


especially calf protein.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

292
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 2 ml ampule 10 and 50 6X, 10
suppositories 6X, 20 capsules 6X.

293
Thymokehl 6X
Suppositories
for rectal application

Active ingredient: Glandula thymi (lyophil., steril.) 6X

Composition: 1 suppository contains: Medically active substance: 0.2 g Glandula


thymi (lyophil., steril.) 6X trit. Other constituents: hard fat, lactose.

According to experience, Disorders in growth and development; adjuvant in anti-carcinogenic


to be administered in therapy; for all degenerative processes in the lumbar vertebral column
cases of: area.

Characteristics: Extracts from organs act positively on the entire cell metabolism. In
cellular therapy, research has shown that materials resorbed from
organ extracts promote cellular repair processes of the DNA. They act
as a stimulant where damaged cells need to be regenerated and as a
supplement where degenerated cells break down. The thymus extract
in Thymokehl shows the same physiological activity; its molecular
structure differs only slightly from the molecular structure of the human
organ. The promotion of cellular respiration by the thymus extract has
been proven in various animal test models.

Application: Unless otherwise prescribed: 1 x daily insert 1 suppository rectally.

Side effects: Because of specific organic components of Thymokehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to foreign protein,


especially calf protein.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

294
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 2 ml ampule 10 and 50 6X, 10
suppositories 6X, 20 capsules 6X.

295
Usneabasan 1X
Drops
Liquid dilution
for oral intake

Active ingredient: Usnea barbata e thallo siccato mother tincture

Composition: 1 ml liquid dilution contain: Medically active substance: 1 ml Usnea


barbata e thallo siccato 1X dil. Other constituents: purified water,
ethanol 62 % (m/m).

According to experience, Congestive headaches; sunstroke; gall bladder disorders; elimination


to be administered in of heavy metals.
cases of:

Characteristics: Usneabasan is a herbal homeopathic remedy from the beardmoss


Usnea barbata. Its main range of application lies in the area of the
head. Usnea barbata has been used in homeopathy for congestive
headaches for a long time. It is also administered for redness of the
face, a knocking or bursting sensation in the temple region, in the eyes
and the back of the head.

Application: Unless otherwise prescribed: in case of acute conditions: up to 6 x daily


5 drops. In case of chronic forms: 1-3 x daily 5 drops.

Side effects: Because of specific organic components of Usneabasan, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: This product contains 70 % (v/v) alcohol (ethanol). This may present
a health risk in cases of liver diseases, alcoholism, epilepsy, brain
damage, pregnancy, and in children. The action of other drugs may be
reduced or intensified.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

296
Advice: This product contains 70 % (v/v) alcohol (ethanol).

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage form is available: 30 ml dropper bottle 1X.

297
Ustilakehl 5X
Ampules
Liquid dilution for injection

Active ingredient: Ustilago zeae e volumine cellulae (lyophil., steril.) 5X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Ustilago


zeae e volumine cellulae (lyophil., steril.) 5X aquous dil. Other
constituents: isotonic sodium chloride solution.

According to experience, Uterine haemorrhage, membranous dysmenorrhoea, menopausal syn-


to be administered in drome, menorrhagia, metrorrhagia; headache caused by menstruation,
cases of: migraine.

Characteristics: Ustilago zeae, the corn-smut, is a parasitary fungus that attacks all
parts of the maize plant and forms bump-like distensions filled with
spore powder. As the maize plant itself, the first medicinal use of the
drug came from America. It was predominantly used in folk medicine by
the Afro-American population. The ergotamine-like action of the corn-
smut in the uterus determines its main effect.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected subcuta-


neously, 1-3 x weekly.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Ustilakehl , theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Ustilago zeae.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Ustilakehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: None.

298
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 5X.

299
Ustilakehl 5X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Ustilago zeae e volumine cellulae (lyophil., steril.) 5X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Ustilago zeae e volumine cellulae (lyophil., steril.) 5X dil. Other
constituents: purified water.

According to experience, Uterine haemorrhage, membranous dysmenorrhoea, menopausal syn-


to be administered in drome, menorrhagia, metrorrhagia; headache caused by menstruation,
cases of: migraine.

Characteristics: Ustilago zeae, the corn-smut, is a parasitary fungus that attacks all
parts of the maize plant and forms bump-like distensions filled with
spore powder. As the maize plant itself, the first medicinal use of the
drug came from America. It was predominantly used in folk medicine by
the Afro-American population. The ergotamine-like action of the corn-
smut in the uterus determines its main effect.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Ustilakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Ustilago


zeae.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Ustilakehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

300
Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 5X.

301
Ustilakehl 5X
Suppositories
for rectal application

Active ingredient: Ustilago zeae e volumine cellulae (lyophil., steril.) 5X

Composition: 1 suppository contains: Medically active substance: 0.2 g Ustilago


zeaee volumine cellulae (lyophil., steril.) 5X trit. Other consti-
tuents: hard fat, lactose.

According to experience, Uterine haemorrhage, membranous dysmenorrhoea, menopausal syn-


to be administered in drome, menorrhagia, metrorrhagia; headache caused by menstruation,
cases of: migraine.

Characteristics: Ustilago zeae, the corn-smut, is a parasitary fungus that attacks all
parts of the maize plant and forms bump-like distensions filled with
spore powder. As the maize plant itself, the first medicinal use of the
drug came from America. It was predominantly used in folk medicine by
the Afro-American population. The ergotamine-like action of the corn-
smut in the uterus determines its main effect.

Application: Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally.


Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Ustilakehl, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to Ustilago


zeae.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Ustilakehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

302
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml
ampule 10 and 50 5X, 10 suppositories 5X.

303
Utilin 4X
Ampules
Liquid dilution for injection

Active ingredient: Bacillus subtilis e volumine cellulae (lyophil., steril.) 4X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Bacillus


subtilis e volumine cellulae (lyophil., steril.) 4X aquous dil..
Other constituents: isotonic sodium chloride solution.

According to experience, All subacute and chronic inflammatory diseases; intestinal dysfunction,
to be administered in liver and gallbladder disorders; for immune modulation; Basedows
cases of: disease; postmenopause disorders.

Characteristics: Utilin is produced from the non-pathogenic microbe Bacillus sub-


tilis. It is applied for modulation of the non-specific immune system.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intra-


muscularly, subcutaneously or intracutaneously, 1-2 x weekly.

Side effects: Because of specific organic components of Utilin, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


Do not administer in cases of known hypersensitivity to Bacillus
subtilis.

Adverse reactions: None known. Generally well tolerated. Occasionally local reactions
like rubefaction, swelling or painfulness may be observed, normally
vanishing without treatment. These effects are not to be seen as
adverse reactions, but rather as an expression of effectiveness. In the
first 2 or 3 days after the injection sometimes conditions of weakness,
fortified expectoration, slight painfulness of the region or subfebrile
temperatures may show. Strong general reactions are always a sign of
overdose or of incorrect injection technique.

Interactions Immunosuppressive drugs can influence the effectivity of Utilin. An


with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

304
Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

305
Utilin 4X
Capsules
for oral intake

Active ingredient: Bacillus subtilis e volumine ex muris cellulae (lyophil., steril.)


4X

Composition: 1 capsule contains: Medically active substance: 330 mg Bacillus


subtilis e volumine ex muris cellulae (lyophil., steril.) 4X trit.
Other constituents: lactose, hypromellosis (capsule shell).

According to experience, All subacute and chronic inflammatory diseases; intestinal dysfunction,
to be administered in liver and gallbladder disorders; for immune modulation; Basedows
cases of: disease; postmenopause disorders.

Characteristics: Utilin is produced from the non-pathogenic microbe Bacillus


subtilis. It is applied for modulation of the non-specific immune
system.

Application: Unless otherwise prescribed: 1-2 x weekly 1 capsule.

Side effects: Because of specific organic components of Utilin, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


Do not administer in cases of known hypersensitivity to Bacillus
subtilis.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Utilin. An


with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

306
Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

307
Utilin 6X
Ampules
Liquid dilution for injection

Active ingredient: Bacillus subtilis e volumine cellulae (lyophil., steril.) 6X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Bacillus


subtilis e volumine cellulae (lyophil., steril.) 6X aquous dil..
Other constituents: isotonic sodium chloride solution.

According to experience, All subacute and chronic inflammatory diseases; intestinal dysfunction,
to be administered in liver and gallbladder disorders; for immune modulation; Basedows
cases of: disease; postmenopause disorders.

Characteristics: Utilin is produced from the non-pathogenic microbe Bacillus


subtilis. It is applied for modulation of the non-specific immune
system.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously or intracutaneously, 1-2 x weekly.

Side effects: Because of specific organic components of Utilin, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


Do not administer in cases of known hypersensitivity to Bacillus
subtilis.

Adverse reactions: Generally well tolerated. Occasionally local reactions like rubefaction,
swelling or painfulness may be observed, normally vanishing without
treatment. These effects are not to be seen as adverse reactions, but
rather as an expression of effectiveness. In the first 2 or 3 days after the
injection sometimes conditions of weakness, fortified expectoration,
slight painfulness of the region or subfebrile temperatures may show.
Strong general reactions are always a sign of overdose or of incorrect
injection technique.

Interactions Immunosuppressive drugs can influence the effectivity of Utilin. An


with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

308
Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

309
Utilin 6X
Capsules
for oral intake

Active ingredient: Bacillus subtilis e volumine ex muris cellulae (lyophil., steril.)


6X

Composition: 1 capsule contains: Medically active substance: 330 mg Bacillus


subtilis e volumine ex muris cellulae (lyophil., steril.) 6X trit.
Other constituents: lactose, hypromellosis (capsule shell).

According to experience, All subacute and chronic inflammatory diseases; intestinal dysfunction,
to be administered in liver and gallbladder disorders; for immune modulation; Basedows
cases of: disease; postmenopause disorders.

Characteristics: Utilin is produced from the non-pathogenic microbe Bacillus


subtilis. It is applied for modulation of the non-specific immune
system.

Application: Unless otherwise prescribed: 1-2 x weekly 1 capsule.

Side effects: Because of specific organic components of Utilin, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


Do not administer in cases of known hypersensitivity to Bacillus
subtilis.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Utilin. An


with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

310
Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

311
Utilin 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Bacillus subtilis e volumine cellulae (lyophil., steril.) 6X

Composition: 5 ml liquid dilution contain: Medically active substance: 5 ml Bacillus


subtilis e volumine cellulae (lyophil., steril.) 6X dil. Other
constituents: purified water.

According to experience, All subacute and chronic inflammatory diseases; intestinal dysfunction,
to be administered in liver and gallbladder disorders; for immune modulation; Basedows
cases of: disease; postmenopause disorders.

Characteristics: Utilin is produced from the non-pathogenic microbe Bacillus


subtilis. It is applied for modulation of the non-specific immune
system.

Application: Unless otherwise prescribed: For oral intake: 1-3 x weekly 2-5 drops.
For rubbing in: 1-3 x weekly 2-5 drops into the bend of the elbow.

Side effects: Because of specific organic components of Utilin, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


Do not administer in cases of known hypersensitivity to Bacillus
subtilis.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Utilin. An


with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

312
Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

313
Utilin 6X
Suppositories
for rectal application

Active ingredient: Bacillus subtilis e volumine ex muris cellulae (lyophil., steril.)


6X

Composition: 1 suppository contains: Medically active substance: 0.2 g Bacillus


subtilis e volumine ex muris cellulae (lyophil., steril.) 6X trit.
Other constituents: hard fat, lactose.

According to experience, All sub-acute and chronic inflammatory diseases, intestinal dysfunction,
to be administered in liver and gallbladder disorders, for immune modulation, Basedows
cases of: disease, postmenopause disorders.

Characteristics: Utilin is produced from the non-pathogenic microbe Bacillus


subtilis. It is applied for modulation of the non-specific immune
system.

Application: Unless otherwise prescribed: 1-3 x weekly insert 1 suppository rectally.

Side effects: Because of specific organic components of Utilin, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


Do not administer in cases of known hypersensitivity to Bacillus
subtilis.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Utilin. An


with other remedies: interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to patients with autoimmune diseases, to women during
pregnancy or breastfeeding, as well as with children.

Advice: This product contains lactose.

314
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

315
Utilin S 4X
Ampules
Liquid dilution for injection

Active ingredient: Mycobacterium phlei e volumine cellulae (lyophil., steril.) 4X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Myco-


bacterium phlei e volumine cellulae (lyophil., steril.) 4X
aquous dil. Other constituents: isotonic sodium chloride solution.

According to experience, All chronic lung diseases; chronic feverish diseases with night sweats
to be administered in and debility, subfebrile temperatures, weakness (for immune modu-
cases of: lation).

Characteristics: Utilin S is produced from the non-pathogenic microbe Myco-


bacterium phlei and has immune-modulating properties.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously or intracutaneously, 1-2 x weekly.

Side effects: Because of specific organic components of Utilin S, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


In cases of known hypersensitivity to Mycobacterium phlei, as a
precaution, this preparation should not be administered.

Adverse reactions: Generally well tolerated. Occasionally local reactions like rubefaction,
swelling or painfulness may be observed, normally vanishing without
treatment. These effects are not to be seen as adverse reactions, but
rather as an expression of effectiveness. In the first 2 or 3 days after the
injection sometimes conditions of weakness, fortified expectoration,
slight painfulness of the region or subfebrile temperatures may show.
Strong general reactions are always a sign of overdose or of incorrect
injection technique.

Interactions Immunosuppressive drugs can influence the effectivity of Utilin S.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

316
Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

317
Utilin S 4X
Capsules
for oral intake

Active ingredient: Mycobacterium phlei e volumine ex muris cellulae (lyophil.,


steril.) 4X

Composition: 1 capsule contains: Medically active substance: 330 mg Bacillus


subtilis e volumine ex muris cellulae (lyophil., steril.) 4X trit.
Other constituents: lactose, hypromellosis (capsule shell).

According to experience, All chronic lung diseases; chronic feverish diseases with night sweats
to be administered in and debility, subfebrile temperatures, weakness (for immune modu-
cases of: lation).

Characteristics: Utilin S is produced from the non-pathogenic microbe Myco-


bacterium phlei and has immune-modulating properties.

Application: Unless otherwise prescribed: 1-2 x weekly 1 capsule.

Side effects: Because of specific organic components of Utilin S, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


In cases of known hypersensitivity to Mycobacterium phlei, as a
precaution, this preparation should not be administered.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Utilin S.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

318
Advice: This product contains lactose.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

319
Utilin S 6X
Ampules
Liquid dilution for injection

Active ingredient: Mycobacterium phlei e volumine cellulae (lyophil., steril.) 6X

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 ml Myco-


bacterium phlei e volumine cellulae (lyophil., steril.) 6X
aquous dil. Other constituents: isotonic sodium chloride solution.

According to experience, All chronic lung diseases; chronic feverish diseases with night sweats
to be administered in and debility, subfebrile temperatures, weakness (for immune modu-
cases of: lation).

Characteristics: Utilin S is produced from the non-pathogenic microbe Myco-


bacterium phlei and has immune-modulating properties.

Application: Unless otherwise prescribed: 1 ampule of 1 ml to be injected either


intramuscularly, subcutaneously or intracutaneously, 1-2 x weekly.

Side effects: Because of specific organic components of Utilin S, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


In cases of known hypersensitivity to Mycobacterium phlei, as a
precaution, this preparation should not be administered.

Adverse reactions: Generally well tolerated. Occasionally local reactions like rubefaction,
swelling or painfulness may be observed, normally vanishing without
treatment. These effects are not to be seen as adverse reactions, but
rather as an expression of effectiveness. In the first 2 or 3 days after the
injection sometimes conditions of weakness, fortified expectoration,
slight painfulness of the region or subfebrile temperatures may show.
Strong general reactions are always a sign of overdose or of incorrect
injection technique.

Interactions Immunosuppressive drugs can influence the effectivity of Utilin S.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

320
Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

321
Utilin S 6X
Capsules
for oral intake

Active ingredient: Mycobacterium phlei e volumine ex muris cellulae (lyophil.,


steril.) 6X

Composition: 1 capsule contains: Medically active substance: 330 mg Bacillus


subtilis e volumine ex muris cellulae (lyophil., steril.) 6X trit.
Other constituents: lactose, hypromellosis (capsule shell).

According to experience, All chronic lung diseases; chronic feverish diseases with night sweats
to be administered in and debility, subfebrile temperatures, weakness (for immune modu-
cases of: lation).

Characteristics: Utilin S is produced from the non-pathogenic microbe Myco-


bacterium phlei and has immune-modulating properties.

Application: Unless otherwise prescribed: 1-2 x weekly 1 capsule.

Side effects: Because of specific organic components of Utilin S, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


In cases of known hypersensitivity to Mycobacterium phlei, as a
precaution, this preparation should not be administered.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Utilin S.


with other remedies: An interval of 4 weeks before and after treatment with administered live
vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

322
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

323
Utilin S 6X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Mycobacterium phlei e volumine cellulae (lyophil., steril.) 6X

Composition: 5 ml liquid dilution contain: Medically active substance: 5 ml


Mycobacterium phlei e volumine cellulae (lyophil., steril.) 6X
dil. Other constituents: purified water.

According to experience, All chronic lung diseases; chronic feverish diseases with night sweats
to be administered in and debility, subfebrile temperatures, weakness (for immune modu-
cases of: lation).

Characteristics: Utilin S is produced from the non-pathogenic microbe Myco-


bacterium phlei and has immune-modulating properties.

Application: Unless otherwise prescribed: For oral intake: 1-3 x weekly 2-5 drops
before a meal. For rubbing in: 1-3 x weekly 2-5 drops into the bend of
the elbow.

Side effects: Because of specific organic components of Utilin S, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


Do not apply to inflamed skin. In cases of known hypersensitivity to
Mycobacterium phlei, as a precaution, this preparation should not
be administered.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Utilin S.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

324
Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

325
Utilin S 6X
Suppositories
for rectal application

Active ingredient: Mycobacterium phlei e volumine ex muris cellulae (lyophil.,


steril.) 6X

Composition: 1 suppository contains: Medically active substance: 0.2 g Myco-


bacterium phlei e volumine ex muris cellulae (lyophil., steril.)
6X trit. Other constituents: hard fat, lactose.

According to experience, All chronic lung diseases; chronic feverish diseases with night sweats
to be administered in and debility, subfebrile temperatures, weakness (for immune modu-
cases of: lation).

Characteristics: Utilin S is produced from the non-pathogenic microbe Myco-


bacterium phlei and has immune-modulating properties.

Application: Unless otherwise prescribed: 1-3 x weekly insert 1 suppository


rectally.

Side effects: Because of specific organic components of Utilin S, theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Fever, conditions of weakness.


In cases of known hypersensitivity to Mycobacterium phlei, as a
precaution, this preparation should not be administered.

Adverse reactions: None known. Generally well tolerated. In the first 2 or 3 days after the
application sometimes conditions of weakness, fortified expectoration
or subfebrile temperatures may show. Strong general reactions are
always a sign of overdose.

Interactions Immunosuppressive drugs can influence the effectivity of Utilin S.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains lactose.

326
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml
ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

327
Verrukehl 5X
Drops
Liquid dilution
for oral intake, rubbing in

Active ingredient: Trichophyton verrucosum e volumine cellulae (lyophil., steril.)


5X

Composition: 10 ml liquid dilution contain: Medically active substance: 10 ml


Trichophyton verrucosum e volumine cellulae (lyophil., steril.)
5X dil. Other constituents: purified water.

According to experience, Trichophytosis, tinea, mycosis of the skin and hair, hair loss.
to be administered in
cases of:

Characteristics: Verrukehl is a remedy produced from the fungus Trichophyton verru-


cosum. It is administered in cases of dermatophyte infections.

Application: Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops. For
rubbing in: 1 x daily 5-10 drops into the bend of the elbow.
Treatment of more than 8 weeks depends on the advice of the physician
or health care professional.

Side effects: Because of specific organic components of Verrukehl; theoretically,


hypersensitivity may occur. In this case, discontinue medication and
treat symptomatically.

Contraindications: Do not administer in cases of known hypersensitivity to mold fungi


Trichophyton verrucosum.

Adverse reactions: None known.

Interactions Immunosuppressive drugs can influence the effectivity of Verrukehl.


with other remedies: An interval of 4 weeks before and after treatment with orally administered
live vaccines must be observed.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: After opening, contents must be used within two months.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 10 ml dropper bottle 5X.

328
Vitamin B Komplex Sanum N
Ampules
Liquid dilution for injection

Active ingredients: Thiamine hydrochloride (vitamin B1), pyridoxine hydrochloride


(vitamin B6)

Composition: 1 ampule of 2 ml contains: Medically active substance: 10 mg thiamine


hydrochloride (vitamin B1), 5 mg pyridoxine hydrochloride
(vitamin B6). Other constituents: benzyl alcohol.

Indication: Neuritis, neuralgia, trigeminal neuralgia, ischialgia, cervical syndrome,


herpes zoster, radiculoneuritis due to degenerative spondylopathy.

Characteristics: Vitamin B1 (thiamine) in its active form, thiamine pyrophosphate


(TPP), plays a crucial role in carbohydrate metabolism. The daily
requirement of vitamin B1 depends on the type of nutrition. If mainly
carbohydrates are consumed, then the required amount of vitamin B1
increases. A pure vitamin B1 deficiency causes reduced mental and
physical power, lack of appetite and muscular atrophy, in particular
of the lower extremities. Vitamin B6 (pyridoxine) is found in all
living cells, and its effective compound, pyridoxal-5-phosphate, is an
indispensable coenzyme in amino acid metabolism. In cases of rich
protein nutrition, the vitamin B6 requirement is increased, as well as
during pregnancy and in cases of hyperthreodism. Vitamin B6 deficiency
can lead to particular forms of anaemia as well as to skin diseases.

Application: Vitamin B Komplex Sanum N has to be injected slowly intravenously


or intramuscularly.
Unless otherwise prescribed: For initial treatment during the first days
of therapy intramuscular injection daily with 1 ampule of 2 ml; after
beginning recovery, 1 ampule of 2 ml 2-3 x weekly.

Side effects: In individual cases, hypersensitivity reactions with urticaria and states
of shock, particularly in allergy prone patients, may occur.
Hypersensitivity caused by benzyl alcohol rarely develops.

Contraindications: Do not administer in cases of known vitamin B1 hypersensitivity.


Vitamin B Komplex Sanum N contains 20 mg benzyl alcohol as
preservative; therefore it must not be administered to new-born and
undeveloped premature babies.

Adverse reactions: None known.

Interactions Vitamin B1 is broken down in infusion solutions containing sulphite.


with other remedies: High dosages of Vitamin B6 can weaken the effect of L-Dopa. In case
of simultaneous use of isoniazid (INH), d-penicillamin and cycloserine,
the effect of vitamin B6 can be lowered.

329
Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 2 ml ampule 10 and 50.

330
Vitamin B 12 Sanum
Ampules
Liquid dilution for injection

Active ingredient: Cyanocobalamin

Composition: 1 ampule of 1 ml contains: Medically active substance: 1 mg Cyano-


cobalamin. Other constituents: sodium chloride, sodium hydroxide
9.5 %, hydrochloric acid 5 %, isotonic sodium chloride solution.

Indications: Vitamin B12 deficiency which cannot be resolved by dietary


measures. Vitamin B12 deficiency can show itself in the following
disorders: hyperchromic, macrocytic megaloblastic anaemia (pernicious
anaemia, Biermers anaemia, addisonian anaemia; these are maturation
disturbances of the erythrocytes); spinal cord damage.
Vitamin B12 deficiency confirmed by laboratory tests can occur in cases
of long lasting malnutrition and malnourishment (e.g. a strict vegetarian
diet); malabsorption (insufficient intestinal absorption of vitamin B12)
caused by insufficient production of intrinsic factor (a protein which is
produced by the gastric mucosa and is necessary for absorption of
vitamin B12), disorders of the ileum (a part of the small intestine), such
as sprue, fish tape worm infestation or blind loop syndrome (obstruction
of the small intestine after abdominal operations); congenital vitamin
B12 transport disorders.

Characteristics: Cyanocobalamin ist gained from bacteria cultures; therefore it is


of plant origin in contrast to hydroxycobalamin from liver extracts.
Numerous metabolic processes in the organism depend on a sufficient
vitamin B12 supply, especially the production of erythrocytes in the
bone marrow, protein synthesis (production of DNA, RNA, growth),
formation of the myelin sheath of the nerve cells, cellular detoxification,
metabolism of fatty acids and folic acid.

Application: Unless otherwise prescribed: For initial treatment during the first weeks of
therapy 1 ampule of 1 ml Vitamin B 12 Sanum (1mg cyanocobalamin)
2 x weekly. In cases of verified intestinal malabsorption of vitamin B12,
subsequent injections with 1000g cyanocobalamin are administered
once a month.
As a rule, Vitamin B 12 Sanum is injected intramuscularly. Slow intra-
venous or subcutaneous injections are also possible.

Side effects: In individual cases, skin reactions (acne as well as eczematous urticarial
drug reactions) and hypersensitivity reactions (anaphylactic and
anaphylacticoid reactions) have occurred.

331
Contraindications: Do not administer in cases of hypersensitivity to vitamin B12 or any
other constituent.

Adverse reactions: None known.

Interactions Due to the instability of Vitamin B12, the addition of other prepara-
with other remedies: tions can lead to loss of effectiveness.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: The recommended daily vitamin B12 intake during pregnancy and
breastfeeding is 4 g. According to previous experience, higher dosages
have no adverse effects on the unborn child. Vitamin B12 passes into
breast milk.
Vitamin B 12 Sanum contains less than 1 mmol (23 mg) sodium
chloride per ampule, i.e. it is almost sodium-chloride-free.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 1 ml ampule 10 and 50.

332
Zinkokehl 3X
Drops
Liquid dilution for oral intake

Active ingredient: Zincum gluconicum 3X

Composition: 1 ml liquid dilution contains: Medically active substance: 0.08 ml


Zincum gluconicum 3X dil. Other constituents: purified water,
ethanol 15 % (m/m).

According to experience, Accompanying treatment for zinc deficiency conditions: bone meta-
be administered in bolism such as coxarthrosis, pseudoarthrosis, rheumatic arthritis,
cases of: psoriatic arthritis; skin diseases such as eczema, acne, slow wound
healing, burns; susceptibility to infections; vegetative dysfunctions,
dysbiosis and consecutive diseases such as cholecystitis, pancreatitis;
diabetes mellitus; vein diseases such as thrombosis and ulcerations of
the lower leg.

Characteristics: Zinc plays a significant role in the bodys metabolism. Chronic zinc
deficiency - caused by poor nutrition or malabsorption can lead to
serious disorders. Zinkokehl contains Zincum gluconicum and is
therefore also suitable for prophylaxis.

Application: Unless otherwise prescribed: For oral intake: in case of acute conditions
every half to one hour, not more than 6 times daily each 5 drops. In case
of chronic conditions 1-3 x daily 5 drops.

Side effects: None known.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: This product contains 20 % (v/v) alcohol (ethanol).


Due to the alcohol content, professional medical advice should be
sought prior to recommending this product to patients with alcohol or
liver problems.

333
Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 30 ml dropper bottle 3X, 2 ml
ampule 10 and 50 4X.

334
Zinkokehl 4X
Ampules
Liquid dilution for injection

Active ingredient: Zincum gluconicum 4X

Composition: 1 ampule of 2 ml contains: Medically active substance: 2 ml Zincum


gluconicum 4X aquous dil. Other constituents: isotonic sodium
chloride solution.

According to experience, Accompanying treatment for zinc deficiency conditions: bone meta-
be administered in bolism such as coxarthrosis, pseudoarthrosis, rheumatic arthritis, pso-
cases of: riatic arthritis; skin diseases such as eczema, acne, slow wound healing,
burns; susceptibility to infections; vegetative dysfunctions, dysbiosis and
consecutive diseases such as cholecystitis, pancreatitis; diabetes melli-
tus; vein diseases such as thrombosis and ulcerations of the lower leg.

Characteristics: Zinc plays a significant role in the bodys metabolism. Chronic zinc
deficiency - caused by poor nutrition or malabsorption can lead to
serious disorders. Zinkokehl contains Zincum gluconicum and is
therefore also suitable for prophylaxis.

Application: Unless otherwise prescribed: 1 ampule of 2 ml to be injected either


intramuscularly, subcutaneously, intracutaneously or intravenously, 1-2 x
daily.

Side effects: None known.

Contraindications: None known.

Adverse reactions: None known.

Interactions
with other remedies: None known.

Precautions: As with all medications and due to the variations of clinical studies,
professional medical advice should be sought prior to recommending
this product to women during pregnancy or breastfeeding, as well as
with children.

Advice: None.

Duration of treatment: Dependent on the advice of the physician or health care professional.

How supplied: The following dosage forms are available: 30 ml dropper bottle 3X, 2 ml
ampule 10 and 50 4X.

335
Disease List
The following information is intended to serve as a quick reference guide for the practi-
tioner and is not intended as a prescription outline. A thorough diagnosis and individual
therapy plan is recommended in each case. It is assumed that through the participation
of seminars specialising in the field of isopathic-homeopathy and pleomorphic research,
that the naturopath gains a clearer insight of this form of therapy.
An intensive introduction and training in SANUM therapy is possible through seminars and
corresponding literature. Contact your distributor for information on future seminars.

Abscess, Allergic Asthma,


Mucokehl, Notakehl, Sanukehl Pseu, Sanu- see Allergy in general, Nigersan
kehl Staph Allergy in general,
Acidosis, Alkala N, Citrokehl, Exmykehl, Formasan,
Alkala N, Citrokehl, Sanuvis Fortakehl, Notakehl, Polysan K, Sanuvis,
Acne, Utilin, Vitamin B Komplex Sanum N
Latensin, Mucokehl, Nigersan, Notakehl, Allergic Diseases of the Gastrointestinal tract,
Pefrakehl, Polysan D, Sanukehl Myc, Sanu- see Allergy in general, Pefrakehl
kehl Staph, Utilin, Zinkokehl
Allergic Rhinitis,
Acne vulgaris, Latensin, Nigersan, Notakehl, Sankombi,
Sanukehl Acne Utilin
Acrodermatitis, Alopecia (Baldness),
Notakehl, Sankombi Mucokehl, Pefrakehl, Pinikehl, Sanukehl
Acrodermatitis enterohepatica, Myc, Sanukehl Strep, Sankombi
Fortakehl, Polysan Dx, Sanukehl Coli, Alopecia areata,
Sanukehl Myc, Zinkokehl
Mucokehl, Pinikehl, Sankombi
Actinomycosis,
Amenorrhea,
Mucokehl, Notakehl, Sanukehl Myc, Sanu-
Nigersan, Recarcin, Sanukehl Myc,
kehl Staph, Utilin S
Ustilakehl
Addisons Disease,
Amoebiasis,
Mucokehl, Nigersan, Recarcin, Sankombi,
Fortakehl, Okoubasan, Sanukehl Coli,
Zinkokehl
Sanukehl Salm
Adenoids,
Mucokehl, Nigersan, Sankombi, Utilin Anal Eczema,
Exmykehl, Fortakehl, Pefrakehl, Sanukehl
Adnexitis, Cand
Fortakehl, Mucokehl, Nigersan, Notakehl,
Pefrakehl, Sanukehl Myc, Sanukehl Strep, Anal Fissures,
Utilin Fortakehl, Mucokehl, Notakehl, Recarcin
Agranulocytosis, Anal Fistula,
Citrokehl, Formasan, Notakehl, Quentakehl, Fortakehl, Mucokehl, Nigersan, Notakehl,
Sanukehl Pseu Pefrakehl, Recarcin, Sanukehl Pseu, Utilin
Alcohol Abuse, Angina Pectoris,
Alkala N, Citrokehl, Mucedokehl, Muscarsan, Leptospermusan, Mucokehl, Nigersan,
Vitamin B Komplex Sanum N Sanoryzae, Sanukehl Acne, Utilin
Alkalinization, Anginal Ulcers (Acute Sore Throat),
Alkala N, Citrokehl, Sanuvis Notakehl, Sankombi, Sanukehl Strep

336
Angioneurotic Edema, Bladder Inflammation,
Fortakehl, Mucedokehl, Polysan Dx, see Cystitis
Strophanthus
Bleeding Tendencies,
Ankle Swelling, Calvakehl
Leptucin, Mucokehl, Mucokehl Atox,
Blepharitis,
Strophanthus
Nigersan, Notakehl, Sanukehl Staph
Anorexia,
Cerivikehl, Citrokehl, Fortakehl Blindness,
Leptospermusan, Mucokehl, Utilin
Anthracosis,
Formasan, Mucokehl, Polysan T, Recarcin, Bloating and Flatulence,
Sanukehl Staph Alkala N, Fortakehl, Pinikehl
Aphasia (see also Stroke), Blood Poisoning,
Mucokehl, Sankombi, Utilin Notakehl, Polysan G, Quentakehl
Aphonia (see also Stroke), Breast Cancer,
Sanukehl Myc Alkala N, Exmykehl, Latensin, Mucokehl,
Aphthous Ulcers, Nigersan, Pefrakehl, Recarcin, Sanukehl
Fortakehl, Mucokehl, Notakehl, Pefrakehl, Pseu, Sanuvis, Selenokehl, Utilin
Quentakehl, Rebas, Recarcin, Sanukehl Bronchiectasis,
Cand, Sankombi Formasan, Notakehl, Sanukehl Klebs
Arrhythmia, Bronchitis,
Mucokehl, Sanukehl Myc, Sanukehl Strep,
Cerivikehl, Mucokehl, Notakehl, Quentakehl,
Strophanthus
Relivora Complex, Sankombi, Ruberkehl,
Arteriosclerosis, Utilin, Utilin S
Citrokehl, Mucokehl, Nigersan, Polysan A,
Sanumgerman, Sanuvis, Utilin Bruises,
Mucokehl, Sanuvis
Artery Disease in general,
Leptucin, Leptospermusan, Mucedokehl, Buccal Mucosal Inflammation,
Mucokehl, Sanukehl Acne, Strophanthus see Stomatitis
Arthritis (Osteoarthritis), Burns,
Arthrokehlan A, Latensin, Lipiscor, Mucokehl, Notakehl, Sanukehl Pseu,
Mucokehl, Nigersan, Notakehl, Polysan D, Sankombi, Zinkokehl
Recarcin, Sankombi, Sanukehl Myc, Utilin, Candidiasis,
Utilin S
Albicansan, Alkala N, Exmykehl, Fortakehl,
Arthrosis, Pefrakehl, Sanukehl Cand
Fortakehl, Latensin, Lipiscor, Notakehl,
Carcinoma,
Recarcin, Utilin S
Arthrokehlan U, Citrokehl, Exmykehl,
Asthma-Bronchitis, Mucokehl, Nigersan, Notakehl, Pefrakehl,
Fortakehl, Latensin, Mucokehl, Nigersan, Polysan K, Polysan Om, Sankombi, Sanuvis,
Notakehl, Sanukehl Myc, Sanukehl Klebs,
Sanukehl Pseu, Sanumgerman, Selenokehl,
Sanukehl Pseu, Utilin, Utilin S, Vitamin B
Utilin, Utilin S, Zinkokehl
Komplex Sanum N
Autonomic Nervous System Dysfunction, Cataract,
Latensin, Mucedokehl, Utilin, Vitamin B Alkala N, Leptucin, Mucokehl (eye drops),
Komplex Sanum N, Zinkokehl Sanuvis, Silvaysan, Utilin S
Avitaminosis, Cell Regeneration Therapy,
Mapurit L, Vitamin B Komplex Sanum N Chrysocor, Citrokehl, Fortakehl,
Balanitis, Leptospermusan, Mucokehl, Nigersan,
Albicansan, Pefrakehl Sanuvis
Bed Wetting, Cephalgia,
Citrokehl, Latensin, Mucedokehl, Sankombi, Alkala N, Citrokehl, Quentakehl, Sanukehl
Sanuvis, Utilin Myc, Usneabasan, Ustilakehl

337
Cervical Syndrome, Chronic Respiratory Tract Diseases,
Notakehl, Quentakehl, Usneabasan, Vitamin Citrokehl, Mucedokehl, Notakehl,
B Komplex Sanum N Ruberkehl, Utilin, Utilin S
Chickenpox, Chronic Rheumatism,
Alkala N, Quentakehl, Sanuvis Arthrokehlan A, Citrokehl, Latensin,
Childhood Diseases, Notakehl, Sanukehl Pseu, Sanumgerman
Latensin, Notakehl, Pefrakehl, Sankombi, Chronic Urinary Tract Infection,
Utilin S Fomepikehl, Nigersan, Notakehl,
Cholangitis, Quentakehl, Sanukehl Coli, Sanukehl Myc
Citrokehl, Fortakehl, Latensin, Mucokehl, Circulatory Problem of the Extremities,
Notakehl, Pinikehl, Sanukehl Coli, Silvaysan, Leptospermusan, Leptucin, Mucedokehl,
Utilin Mucokehl, Sanukehl Acne, Sanumgerman,
Cholecystitis, Strophanthus
Albicansan, Fortakehl, Mucokehl, Notakehl, Circulatory Problems in general,
Pinikehl, Sanukehl Coli, Sanukehl Myc, Alkala N, Leptospermusan, Leptucin,
Utilin, Usneabasan, Zinkokehl Mucokehl, Sankombi, Sanuvis
Chondrodystrophy, Coeliac Disease,
Citrokehl, Latensin, Mapurit L, Mucokehl, Exmykehl, Fortakehl, Mucokehl, Nigersan,
Nigersan, Utilin, Utilin S Notakehl, Polysan Dx, Recarcin, Sanukehl
Coli, Sanukehl Pseu, Sanukehl Salm,
Chronic Bronchitis,
Sanukehl Staph
Cerivikehl, Fortakehl, Latensin, Quentakehl,
Recarcin, Sanukehl Pseu, Utilin, Utilin S Colds,
Notakehl, Quentakehl, Polysan G, Relivora
Chronic Dermatitis (Dermopathy),
Komplex, Sanukehl Serra
Citrokehl, Latensin, Mucokehl, Pefrakehl,
Sanukehl Pseu, Sanuvis, Utilin Colitis ulcerosa Syndrome,
Albicansan, Exmykehl, Fortakehl,
Chronic Dermatosis,
Latensin, Leptospermusan, Mucokehl,
Utilin, Zinkokehl
Nigersan, Notakehl, Rebas, Recarcin,
Chronic Gastrointestinal Tract Inflammation, Sanukehl Brucel, Sanukehl Cand, Sanukehl
Fortakehl, Pefrakehl, Sanukehl Salm, Coli, Sanukehl Myc, Utilin, Utilin S
Recarcin, Utilin
Collagen Diseases,
Chronic Hepatitis, Arthrokehlan A, Citrokehl, Fortakehl,
Pinikehl, Rebas, Sankombi, Silvaysan, Utilin Latensin, Sanukehl Pseu, Sanuvis
Chronic Inflammation, Colon Cancer (see also Cacinoma),
Fortakehl, Latensin, Notakehl, Recarcin, Arthrokehlan A, Exmykehl, Fortakehl,
Sanukehl Pseu, Utilin S Latensin, Mapurit L, Mucokehl, Nigersan,
Chronic Intestinal Diseases, Notakehl, Pefrakehl, Recarcin, Sanukehl
Exmykehl, Fortakehl, Latensin, Sanukehl Pseu, Sanuvis, Selenokehl, Utilin S
Brucel, Sanukehl Cand, Sanukehl Coli, Congestive Heart Failure,
Sanukehl Salm, Sanukehl Prot, Utilin Calvakehl, Leptospermusan, Strophanthus
Chronicity in general, Conjunctivitis,
Arthrokehlan U, Citrokehl, Fortakehl, Citrokehl, Fortakehl, Leptospermusan,
Lipiscor, Mapurit L, Pinikehl, Sankombi Luffasan, Mucokehl (eye drops), Notakehl,
Chronic Mucosal Inflammation, Ruberkehl, Sanukehl Myc, Sanuvis
Fortakehl, Latensin, Recarcin, Relivora Constipation,
Complex Exmykehl, Fortakehl, Leptospermusan,
Chronic Pancreatitis, Mucokehl, Sanukehl Cand, Utilin
Alkala N, Citrokehl, Fortakehl, Pefrakehl, Convalescence,
Pinikehl, Recarcin, Sanukehl Salm see recovery

338
Coronary Circulation Problems (see Duodenal Ulcer,
Artery Disease in general), Fortakehl, Latensin, Recarcin, Sanukehl
Leptospermusan, Leptucin, Mapurit L, Myc, Sanukehl Prot, Utilin S
Mucokehl, Sankombi, Sanukehl Acne, Dupuytrens Contracture,
Strophanthus Mucokehl, Nigersan, Polysan Dx, Utilin
Corns and Calluses, Dysbiosis,
Mucokehl, Notakehl, Sanuvis, Utilin Albicansan, Citrokehl, Fortakehl, Notakehl,
Crohns Disease, Pefrakehl, Sanukehl Myc, Sanukehl Prot,
Fortakehl, Latensin, Mucokehl, Nigersan, Sanuvis, Zinkokehl
Polysan A, Recarcin, Sanukehl Brucel, Dysfunction of the male Gonads from
Sanukehl Myc, Utilin S diseases or aging,
Cystitis, Chrysocor, Citrokehl, Mucokehl, Nigersan,
Citrokehl, Fortakehl, Leptucin, Notakehl, Sanuvis
Pefrakehl, Ruberkehl, Sanukehl Coll, Dysmenorrhea,
Sanukehl Myc, Sanuvis Chrysocor, Mucedokehl, Mucokehl, Nigersan,
Dacryocystitis, Recarcin, Sankombi, Ustilakehl, Utilin
Citrokehl, Mucokehl, Nigersan, Notakehl, Ear Inflammation,
Sanukehl Staph, Sanukehl Strep see otitis
Degenerative Diseases of the Vertebrae Easy Fatigability,
and the Joints, Bovisan, Citrokehl, Silvaysan
Arthrokehlan A, Notakehl, Vitamin B Eczema,
Komplex Sanum N Latensin, Notakehl, Pefrakehl, Polysan T,
Dental Granuloma, Recarcin, Sankombi, Sanukehl Cand,
Arthrokehlan U, Notakehl, Sankombi Sanukehl Myc, Sanukehl Strep, Sanuvis,
Utilin, Vitamin B Komplex Sanum N,
Dermatophytosis (Skin Fungal Infection),
Zinkokehl
Albicansan, Fortakehl, Pefrakehl, Sanukehl
Cand, Sanukehl Trich Elimination Therapy,
Luffasan, Okoubasan, Selenokehl,
Diabetes Mellitus,
Usneabasan, Zinkokehl
Fortakehl, Grifokehl, Latensin, Mucokehl,
Nigersan, Sankombi, Sanukehl Coli, Utilin, Embolism,
Utilin S, Zinkokehl Mucokehl, Sanukehl Acne, Sanuvis, Utilin S
Diabetic Gangrene, Empyema,
Leptucin, Mucokehl, Nigersan, Pinikehl, Notakehl, Sanukehl Salm, Sanukehl Staph,
Sankombi, Sanukehl Acne, Utilin, Utilin S Sanukehl Strep, UtilinS

Diarrhea, Encephalitis,
Calvakehl, Exmykehl, Fortakehl, Nigersan, Latensin, Notakehl, Quentakehl, Utilin,
Okoubasan Utilin S
Endocarditis,
Dislocation,
Mucokehl, Notakehl, Quentakehl, Sanukehl
see distortions
Staph, Sanukehl Strep, Utilin
Distortions,
Endometritis,
Mucokehl, Sankombi, Sanuvis
Alkala N, Calvakehl, Fortakehl, Mucokehl,
Diverticulitis, Nigersan, Notakehl, Sanuvis
Fortakehl, Mucedokehl, Mucokehl, Notakehl,
Enteritis,
Sanukehl Myc, Sanukehl Pseu, Sanuvis
Fortakehl, Okoubasan, Pefrakehl,
Drug Abuse, Usneabasan, Utilin S
Citrokehl, Mucedokehl, Muscarsan
Epicondylitis,
Dry Cough, Fortakehl, Mucokehl, Nigersan, Notakehl,
Cerivikehl, Notakehl, Relivora Complex Sanuvis, Utilin, Utilin S

339
Epididymitis, Furunculosis (Boils),
Citrokehl, Latensin, Mucokehl, Nigersan, Latensin, Mucokehl, Notakehl, Sanukehl
Notakehl, Quentakehl, Sanukehl Coli, Pseu, Sanukehl Salm, Sanukehl Staph, Utilin
Sanukehl Myc Gallbladder Disease,
Epilepsy, Alkala N, Fortakehl, Latensin, Pinikehl,
Mucedokehl, Mucokehl, Muscarsan, Recarcin, Silvaysan, Utilin
Nigersan, Sanumgerman, Utilin Ganglion Cyst,
Erysipelas, Latensin, Nigersan, Recarcin, Sankombi,
Latensin, Notakehl, Quentakehl, Sanukehl Sanuvis, Utilin
Strep, Utilin Gastric Mucosal Diseases,
Erythema nodosum, Alkala N, Fortakehl, Latensin, Recarcin,
Bovisan, Sanukehl Strep, Utilin S Sanukehl Prot
Extrapulmonary Tuberculosis, Gastric Mucosal Inflammation,
Nigersan, Sanukehl Myc, Utilin S see gastritis
Exudative Erythema Multiforme, Gastric Ulcer,
Nigersan, Utilin S Alkala N, Fortakehl, Latensin, Mucokehl,
Recarcin, Sanukehl Myc, Sanukehl Prot,
Eye (Inflammation of), Sanuvis, Utilin
Mucokehl, Mucokehl (eye drops), Notakehl
Gastritis,
Femoral Artery and Vein Diseases (see Alkala N, Fortakehl, Latensin,
Artery Diseases in general), Leptospermusan, Mucedokehl, Mucokehl,
Mucokehl, Sanukehl Acne, Sanuvis Recarcin, Sanukehl Myc, Sanukehl Prot,
Fever, Sanuvis, Utilin
Larifikehl, Notakehl, Polysan G, Quentakehl, Gastroenteritis,
Relivora Complex, Utilin S Citrokehl, Fortakehl, Latensin, Okoubasan,
Fibromyalgia, Pefrakehl, Sanukehl Coli, Sanukehl Salm
Fortakehl, Latensin, Quentakehl, Sanukehl Gastrointestinal Dysfunction,
Myc, Sanukehl Pseu Citrokehl, Fortakehl, Pefrakehl, Pinikehl,
Fissures, Okoubasan, Sanuvis
see rhagades Gastrointestinal Tract Disease,
Flatulence and Bloating, Alkala N, Calvakehl, Fortakehl, Latensin,
Alkala N, Fortakehl, Pinikehl Leptospermusan, Mucokehl, Rebas,
Recarcin, Sanuvis, Utilin
Folliculosis,
Mapurit L, Notakehl, Sanukehl Staph Gastrointestinal Tract Infection,
Fortakehl, Okoubasan, Quentakehl
Food Poisoning,
Gastrointestinal Tract Inflammation,
Okoubasan
Fortakehl, Latensin, Recarcin, Sanukehl Prot
Fractures,
Generalized Itchiness
Citrokehl, Mucokehl, Nigersan, Sanuvis,
(see Allergy in general),
Utilin, Zinkokehl
Fortakehl, Pefrakehl, Sanukehl Cand,
Frequent Infections, Sanukehl Pseu, Sanuvis
(see Susceptibility to Infection)
Genital Herpes (see Herpes in general),
Fortakehl, Sankombi, Utilin, Zinkokehl
Alkala N, Latensin, Mucokehl, Nigersan,
Frostbite, Quentakehl, Sanukehl Prot, Stolonikehl
Leptucin, Mucokehl, Nigersan, Sanuvis, Utilin Genital Itchiness,
Functional Heart Complaints, Albicansan, Alkala N, Fortakehl, Pefrakehl,
Fortakehl, Mucokehl, Sanuvis, Strophanthus Sanukehl Cand, Silvaysan
Fungal Infections in general, Genital Mycosis (see mycosis in general),
Albicansan, Exmykehl, Fortakehl, Nigersan, Albicansan, Exmykehl, Pefrakehl, Sanukehl
Notakehl, Pefrakehl, Sanukehl Cand Cand

340
Gingivitis, Herpes zoster,
Albicansan, Fortakehl, Latensin, Mucokehl, Notakehl, Quentakehl, Sanukehl Prot,
Nigersan, Notakehl, Pefrakehl, Sanukehl Sanuvis, Stolonikehl, Vitamin B Komplex
Cand, Utilin Sanum N
Glaucoma, Hodgkins Lymphogranulomatosis,
Mucokehl, Mucokehl (eye drops), Sanuvis, Latensin, Mucokehl, Nigersan, Notakehl,
Utilin S Sanukehl Pseu, Sanuvis, Utilin
Gonorrhea, Hydrocoele,
Notakehl, Polysan E, Utilin S Nigersan, Notakehl, Sanukehl Myc
Gout, Hyperlipidemia,
Alkala N, Mucokehl, Recarcin, Sankombi, Lipiscor, Mucokehl, Nigersan, Sanuvis
Sanuvis, Utilin Hypertension,
Graves Disease (Exophtalmic Goiter), Lipiscor, Mucokehl, Utilin, Sanoryzae,
Latensin, Mucokehl, Nigersan, Notakehl, Sanuvis
Sankombi, Utilin, Utilin S Hyperthyroidism,
Growth and Developmental Disorders, Mucokehl, Nigersan, Notakehl, Sankombi,
Citrokehl, Fortakehl, Sanukehl Salm, Utilin, Utilin S
Thymokehl Hyperthrophy of the Tonsils,
Hair loss (see Alopecia), Bovisan, Mucokehl, Nigersan, Notakehl
Notakehl, Pleo Chelate, Sanukehl Myc, Hypogonadism,
Sanukehl Trich, Selenokehl, Vitamin B Chrysocor, Citrokehl, Mucokehl, Nigersan
Komplex Sanum N, Zinkokehl
Hypotension,
Hay Fever (see Allergy in general), Mucokehl, Polysan K, Selenokehl,
Luffasan, Ruberkehl, Sanukehl Pseu, Utilin S
Headache, Hypoxia,
see cephalgia Calvakehl
Heartburn, Ichthyosis (Dry scaly skin),
Alkala N, Fortakehl, Sanukehl Myc, Nigersan, Notakehl, Sankombi, Sanuvis,
Sanukehl Strep, Strophanthus Utilin, Utilin S
Heavy metal burden, Immunomodulation,
Mapurit L, Okoubasan, Pleo Chelate, Arthrokehlan U, Bovisan, Episcorit,
Selenokehl, Usneabasan, Zinkokehl Fomepikehl, Grifokehl, Latensin, Leptucin,
Hematoma (Bruises), Recarcin, Relivora Complex, Sanukehl Pseu,
Mucokehl, Sanuvis Utilin, Utilin S
Hemiplegia, Impetigo,
Leptucin, Mucokehl, Sankombi, Sanukehl Latensin, Notakehl, Sanukehl Staph, Utilin,
Acne, Sanuvis, Utilin Utilin S
Hemorrhagic Rhinitis, Induratio penis,
Calvakehl, Mucokehl, Sanuvis, Ustilakehl Mucokehl, Nigersan, Sanuvis
Hemorrhoids, Infarct, Status post,
Mucokehl, Notakehl, Sanuvis Leptucin, Mucokehl, Sankombi, Sanukehl
Hepatitis B, Acne, Sanukehl Strep, Sanuvis
Fortakehl, Leptucin, Pinikehl, Rebas, Infectious Diseases,
Sankombi, Silvaysan, Utilin Alkala N, Fortakehl, Notakehl, Quentakehl,
Herpes in general, Sanuvis
Latensin, Notakehl, Quentakehl, Sankombi, Infectious Skin Disease,
Sanukehl Prot, Stolonikehl, Vitamin B Albicansan, Notakehl, Pefrakehl, Sanuvis,
Komplex Sanum N Utilin

341
Infertility, Joint Diseases,
Chrysocor, Fortakehl, Latensin, Mucokehl, Latensin, Notakehl, Recarcin, Sanukehl
Nigersan, Sankombi, Sanuvis, Selenokehl Strep
Inflammation after BCG Vaccination, Keloid,
Bovisan, Citrokehl, Nigersan Mucokehl, Sanukehl Pseu
Inflammation in general, Keratitis,
Latensin, Leptospermusan, Mucokehl, Mucokehl, Sanukehl Myc
Notakehl, Polysan G, Rebas Kraurosis vulvae,
Inflammation of the Biliary Tract, Citrokehl, Nigersan, Sanukehl Myc
Citrokehl, Fortakehl, Latensin, Mucokehl, Landry Palsy (Guillian Barre Syndrome),
Notakehl, Pinikehl, Sanukehl Coli, Sanukehl Exmykehl, Lipiscor, Notakehl, Quentakehl,
Myc, Utilin Sankombi, Utilin S, Vitamin B Komplex
Inflammation of the Digestive Organs Sanum N
(see gastritis, Crohns Disease, Colitis Laryngeal Ulceration,
ulcerosa), Notakehl, Quentakehl, Recarcin, Sanukehl
Fortakehl, Larifikehl, Latensin, Mucokehl, Myc
Sanukehl Myc, Sanukehl Pseu, Sanuvis,
Utilin Laryngitis,
Cerivikehl, Nigersan, Notakehl, Quentakehl
Inflammatory Process of the Stomach,
Citrokehl, Cuprukehl, Fortakehl, Latensin, Leg Cramps,
Notakehl, Recarcin, Sanukehl Prot Latensin, Mapurit L, Mucokehl

Influenza Infection, Leukemia,


Polysan G, Quentakehl, Ruberkehl, Citrokehl, Mucokehl, Nigersan, Sankombi,
Sanukehl Klebs, Sanuvis Sanuvis

Inherited Toxins, Leukopenia,


Polysan E, Utilin S Latensin, Mucokehl, Nigersan, Pinikehl,
Sanukehl Pseu, Sanuvis
Insect Bites,
Notakehl, Sankombi, Sanukehl Pseu, Libido Problems,
Sanuvis Chrysocor, Citrokehl, Ginkgobakehl,
Mapurit L, Nigersan, Selenokehl
Intercostal Neuralgia,
Citrokehl, Notakehl, Quentakehl, Sanuvis, Lichen ruber (Acuminatus Pityriasis),
Stolonikehl Latensin, Mucokehl, Nigersan, Sanukehl
Trich, Sanuvis, Utilin, Zinkokehl
Intermittent Claudication,
see smokers Leg Lipomatosis, Lipomas,
Citrokehl, Latensin, Lipiscor, Mucokehl,
Intermittent Fever, Nigersan, Recarcin, Sanuvis, Utilin S
Pinikehl, Polysan M, Sanukehl Brucel
Liver Cancer (see Carcinoma),
Intestinal Dysfunction, Chrysocor, Exmykehl, Latensin, Lipiscor,
Fortakehl, Utilin Mucokehl, Nigersan, Recarcin, Sanukehl
Intestinal Yeast Infection, Pseu, Sanuvis
Albicansan, Exmykehl, Fortakehl, Liver Cirrhosis,
Pefrakehl, Sanukehl Cand Citrokehl, Mucokehl, Nigersan, Notakehl,
Intestinal Tuberculosis, Pinikehl, Recarcin, Sanuvis, Silvaysan
Citrokehl, Latensin, Nigersan, Sanukehl Liver Disease,
Myc, Utilin S Alkala N, Latensin, Notakehl, Pinikehl,
Intoxication, Rebas, Sankombi, Sanuvis, Silvaysan,
Okoubasan Utilin
Iridocyclitis, Liver Parenchymal Disorder,
Mucokehl, Nigersan, Notakehl, Sanuvis Sankombi, Selenokehl, Silvaysan, Utilin

342
Lobar Pneumonia Male Menopausal Syndrome,
(see Pneumonia in general), Alkala N, Chrysocor, Mucedokehl, Nigersan,
Citrokehl, Fortakehl, Nigersan, Notakehl, Sanuvis, Silvaysan
Polysan Dx, Polysan T, Sanukehl Klebs,
Malignant Melanoma,
Sanukehl Staph
see carcinoma
Low Energy/Performance Levels,
Mastitis,
Chrysocor, Citrokehl, Mapurit L, Selenokehl
Mucokehl, Notakehl, Sanukehl Staph,
Lumbago, Sanukehl Strep
Notakehl, Nigersan, Recarcin, Utilin,
Vitamin B Komplex Sanum N Mastoiditis,
Mucokehl, Nigersan, Notakehl, Sanukehl
Lung Abscess, Staph
Larifikehl, Mucokehl, Notakehl, Sanukehl
Myc, Sanukehl Pseu Measles,
Notakehl, Quentakehl, Utilin
Lung Cancer,
Fortakehl, Mucokehl, Nigersan, Notakehl, Menires Disease,
Pefrakehl, Recarcin, Sankombi, Sanukehl Mucokehl, Quentakehl, Sanukehl Prot
Myc, Sanukehl Pseu, Sanuvis, Utilin S Meningitis,
Lung Diseases, Latensin, Notakehl, Quentakehl, Sanukehl
Cerivikehl, Citrokehl, Larifikehl, Nigersan, Staph, Sanukehl Strep, Utilin S
Notakehl, Utilin S Menopausal Symptoms,
Lung Emphysema, Mucokehl, Sankombi, Ustilakehl, Utilin
Fortakehl, Larifikehl, Latensin, Mucokehl, Menorrhagia (Excessive Menstruation),
Nigersan, Sanukehl Myc, Utilin Calvakehl, Ustilakehl
Lupus,
Metabolic Disorders,
Fortakehl, Latensin, Mucokehl, Nigersan,
Citrokehl, Mapurit L, Polysan A, Sanuvis,
Pefrakehl, Recarcin, Sanukehl Myc, Sanuvis,
Selenokehl, Silvaysan
Utilin, Utilin S
Metritis (Inflammation of the Uterus),
Lyme Disease/Borreliosis,
Fortakehl, Notakehl, Sankombi, Sanukehl
Alkala N, Fortakehl, Mucokehl, Nigersan,
Coll, Sanukehl Myc
Notakehl, Sanukehl Brucel, Utilin S
Lymphadenitis (Lymph Node Swelling), Metrorrhagia (Uterine Bleeding),
Latensin, Mucokehl, Nigersan, Notakehl, Calvakehl, Ustilakehl
Pefrakehl, Recarcin, Sanoryzae, Sanuvis, Middle Ear Infections,
Utilin S see otitis media
Lymphatic Constitution, Migraine,
Nigersan, Pefrakehl, Sankombi, Sanoryzae, Alkala N, Latensin, Leptospermusan,
Sanuvis Luffasan, Mucokehl, Quentakehl,
Lymphoma, Polysan T, Sanukehl Strep, Sanuvis,
Latensin, Mucokehl, Nigersan, Sankombi, Selenokehl, Silvaysan, Usneabasan,
Utilin Ustilakehl
Lymphostasis, Mouth Diseases,
Mucedokehl, Mucokehl, Nigersan Albicansan, Notakehl, Pefrakehl, Sanukehl
Magnesium Deficiency (Malabsorbtion), Cand, Sanukehl Myc
Mapurit L Multiple Sclerosis,
Malaria, Status Post, Exmykehl, Latensin, Mucokehl, Nigersan,
Citrokehl, Fortakehl, Mucokehl, Nigersan, Notakehl, Pleo Chelate, Quentakehl,
Notakehl, Polysan M, Sanukehl Brucel, Recarcin, Sanumgerman, Sanuvis,
Sanuvis, Utilin S Stolonikehl, Utilin

343
Myalgia (Muscle Pains), Oophoritis (Inflammation of the Ovaries),
Arthrokehlan A, Larifikehl, Mapurit L, Mucokehl, Notakehl, Quentakehl, Recarcin
Sanukehl Brucel, Sanuvis, Vitamin B Osteochondritis,
Komplex Sanum N Citrokehl, Latensin, Nigersan, Notakehl,
Mycosis in general, Utilin
Albicansan, Exmykehl, Nigersan, Notakehl,
Osteochondrosis,
Sankombi, Pefrakehl, Sanukehl Cand
Latensin, Nigersan, Notakehl, Sanukehl
Myocardial Infarction, Myc, Utilin S
Alkala N, Leptospermusan, Mucokehl,
Osteomyelitis,
Sanukehl Acne, Sanuvis
Mucokehl, Notakehl, Quentakehl, Sanukehl
Myocarditis, Prot, Sanukehl Staph, Sanukehl Strep,
Mucokehl, Notakehl, Quentakehl, Sanukehl Utilin S
Strep
Osteoporosis,
Nasal Mucosa Inflammation, Alkala N, Citrokehl, Fortakehl, Latensin,
Luffasan, Mucedokehl, Notakehl, Nigersan, Recarcin, Sankombi, Sanuvis,
Quentakehl, Recarcin, Ruberkehl Utilin
Nephritis,
Ostitis,
Cuprukehl, Latensin, Mucokehl, Nigersan,
Citrokehl, Mucedokehl, Mucokehl, Notakehl,
Notakehl, Quentakehl, Ruberkehl,
Sankombi, Sanuvis, Utilin
Sankombi, Sanukehl Myc, Sanukehl Staph,
Sanuvis, Utilin Otitis externa,
Notakehl, Pefrakehl
Nephrosis,
Latensin, Notakehl, Pefrakehl, Quentakehl, Otitis media,
Ruberkehl, Sanuvis Mucokehl, Nigersan, Notakehl, Recarcin,
Nerve Inflammation, Sanukehl Pseu, Sanukehl Strep, Sankombi,
see neuritis Utilin

Neuralgia, Otosclerosis,
Mapurit L, Notakehl, Polysan R, Quentakehl, Citrokehl, Mucokehl, Nigersan, Polysan E,
Selenokehl, Vitamin B Komplex Sanum N Utilin
Neurodermatitis, Ovarian Cyst,
Fortakehl, Latensin, Mucokehl, Nigersan, Citrokehl, Mucokehl, Nigersan, Utilin,
Notakehl, Sanuvis, Utilin, Utilin S Utilin S
Neuromuscular Disorders, Pancreatic Insufficiency,
Cerivikehl, Latensin, Mapurit L, Okoubasan Alkala N, Citrokehl, Fortakehl, Nigersan,
Neuropathy, Pinikehl, Silvaysan
Mucedokehl, Notakehl, Polysan A, Sanukehl Pancreatitis,
Acne, Selenokehl, Stolonikehl Fortakehl, Mucokehl, Nigersan, Notakehl,
Neuritis, Quentakehl, Recarcin, Sanuvis, Zinkokehl
Mapurit L, Mucokehl, Notakehl, Recarcin, Paradentosis,
Sankombi, Utilin, Utilin S, Vitamin B Citrokehl, Nigersan, Notakehl, Pefrakehl,
Komplex Sanum N, Zinkokehl Pleo Chelate, Polysan A
Nodules, Paratubercular Inflammation,
Sanukehl Coli, Utilin Bovisan, Fortakehl, Nigersan, Sankombi,
Nose Bleeding, Utilin
Calvakehl Parkinsons Disease,
Obesity, Fortakehl, Latensin, Leptucin, Mapurit L,
Alkala N, Grifokehl, Latensin, Mucedokehl, Mucedokehl, Mucokehl, Nigersan, Sanukehl
Muscarsan, Nigersan, Utilin, Utilin S Acne, Utilin

344
Pemphigus vulgaris, Precancerous Stages,
Mucokehl, Pefrakehl, Quentakehl, Utilin S Fortakehl, Mapurit L, Polysan Om,
Perianal Eczema, Sanukehl Pseu, Selenokehl, Utilin S,
Pefrakehl, Utilin, Albicansan Zinkokehl

Pericarditis, Pre- and Post-operative Phase,


Chrysocor, Cuprukehl, Mucokehl, Sanuvis
Mucokehl, Notakehl, Quentakehl, Sanukehl
Strep, Strophanthus Pregnancy,
Sankombi, Sanuvis
Peripheral Vascular Disease,
Ginkgobakehl, Leptospermusan, Leptucin, Problems of the Elderly,
Mucokehl, Sanukehl Acne, Sanukehl Prot Chrysocor, Citrokehl, Latensin, Mucokehl,
Nigersan, Polysan A, Sankombi, Sanuvis,
Peritonsillitis,
Selenokehl, Utilin
Notakehl, Sanukehl Prot
Progressive Chronic Polyarthritis,
Pernicious Anemia, see rheumatoid arthritis
Fortakehl, Mucokehl, Sanuvis, Utilin,
Vitamin B Komplex Sanum N Prostatic Adenoma and Hypertrophy,
Exmykehl, Fomepikehl, Mucokehl, Nigersan,
Perthess Disease, Notakehl, Sanuvis
Citrokehl, Latensin, Nigersan, Utilin
Prostatic Cancer,
Pertussis, Exmykehl, Fomepikehl, Mucokehl, Nigersan,
Quentakehl, Recarcin, Relivora Complex, Notakehl, Sankombi, Sanukehl Pseu
Ruberkehl
Prostatitis,
Peyronies Disease, Exmykehl, Mucokehl, Nigersan, Notakehl,
see lnduratio penis Pefrakehl, Polysan A, Sanukehl Coli
Pharyngitis, Psoriasis,
Notakehl, Quentakehl, Sanukehl Pseu, Fortakehl, Latensin, Mucokehl, Notakehl,
Utilin S Recarcin, Sanukehl Myc, Sanuvis, Utilin,
pH Regulation, Utilin S
Alkala N, Citrokehl, Sanuvis Psoriatic Arthritis,
Pleuritis, Fortakehl, Larifikehl, Latensin, Recarcin,
Nigersan, Notakehl, Sanukehl Myc, Utilin S, Zinkokehl
Sanukehl Klebs Pyelocystitis and -nephritis,
Pneumoconiosis, Citrokehl, Nigersan, Notakehl, Sanukehl
Notakehl, Sanukehl Klebs Coli, Sanukehl Myc, Sanukehl Prot, Sanuvis
Pneumonia, Pyloric Spasm,
Citrokehl, Nigersan, Notakehl, Sanukehl Fortakehl, Leptospermusan, Mucedokehl
Coli, Sanukehl Klebs, Sanukehl Staph, Pyoderma,
Sanukehl Strep, Utilin Mucokehl, Notakehl, Pefrakehl, Sankombi,
Polyarthritis, Utilin
Larifikehl, Mucokehl, Nigersan, Notakehl, Raynauds Disease,
Recarcin, Sanukehl Brucel, Sanukehl Myc, Leptucin, Mucokehl, Sanukehl Acne,
Sanuvis, Utilin S Sanuvis
Poor Bone and Cartilage Growth and Recovery,
Healing, Latensin, Mucokehl, Zinkokehl
Nigersan, Selenokehl, Utilin, Zinkokehl Rectal Cancer,
Post Alcohol Abuse, see Carcinoma
Muscarsan, Alkala N, Mucedokehl, Citrokehl Reiters Disease,
Post Menopausal Syndrome, Fortakehl, Latensin, Mucokehl, Notakehl,
Chrysocor, Ustilakehl, Utilin Recarcin, Utilin

345
Respiratory Diseases, Skin and Conjunctival Tuberculosis,
Alkala N, Cerivikehl, Citrokehl, Formasan, Nigersan, Sanukehl Acne, Utilin S
Latensin, Luffasan, Mucedokehl, Notakehl, Skin Diseases,
Sankombi, Sanukehl Klebs Calvakehl, Pefrakehl, Sanuvis, Utilin,
Respiratory Inflammation, Zinkokehl,
Notakehl, Quentakehl, Relivora Complex Sleep Disturbance,
Rheumatic Fever (see Rheumatism), Fortakehl, Leptospermusan
Fortakehl, Notakehl, Sanukehl Salm Smokers Leg,
Rheumatism, Leptucin, Mucokehl, Sanukehl Acne,
Alkala N, Arthrokehlan A, Bovisan, Sanuvis
Citrokehl, Latensin, Mucokehl, Nigersan, Spherocytosis,
Polysan R, Polysan T, Recarcin, Sankombi, Fortakehl, Mucokehl, Nigersan, Pefrakehl,
Utilin, Utilin S, Vitamin B Komplex Vitamin B Komplex Sanum N
Sanum N
Spleen Diseases,
Rheumatoid Arthritis, Mucokehl, Okoubasan, Pinikehl, Sanuvis
Fortakehl, Latensin, Nigersan, Notakehl,
Recarcin, Sanukehl Acne, Utilin, Vitamin B Spondylopathy,
Komplex Sanum N, Zinkokehl Citrokehl, Latensin, Nigersan, Notakehl,
Quentakehl
Rhinitis,
Fortakehl, Latensin, Luffasan, Mucokehl, Sprains,
Nigersan, Quentakehl, Recarcin, Ruberkehl, Mucokehl
Sanukehl Myc, Sanuvis, Utilin Stimulation of Blood Cell Production,
Salpingitis, Citrokehl, Leptucin, Mucokehl, Sanuvis
Notakehl, Sanukehl Coli Stomatitis,
Scarlet Fever, Albicansan, Notakehl, Pefrakehl,
Mucokehl, Notakehl, Sanukehl Strep, Quentakehl, Recarcin, Sanukehl Cand,
Utilin Utilin
Scheuermanns Disease, Stroke,
Citrokehl, Latensin, Mucokehl, Nigersan, Leptospermusan, Leptucin, Mucokehl,
Sanuvis Sanukehl Acne, Sanuvis, Utilin
Sciatica (Sciatic Nerve Pain), Stye,
Mucokehl, Notakehl, Utilin, Vitamin B Notakehl, Sanukehl Myc, Sanukehl Staph
Komplex Sanum N Sunstroke,
Scintillating Scotoma, Usneabasan, Mucokehl, Sanuvis
Mucokehl (eye drops) Suppurations,
Septic Fever, Notakehl, Polysan G
Alkala N, Citrokehl, Fortakehl, Nigersan, Susceptibility to Infection,
Notakehl, Pefrakehl, Pinikehl, Quentakehl, Fortakehl, Quentakehl, Sankombi, Sanukehl
Sanuvis Serra, Utilin S
Silicosis,
Symbiotic Therapy (Symbiosis)
Citrokehl, Mucokehl, Nigersan, Sanukehl
(see Dysbiosis),
Klebs
Fortakehl, Pefrakehl, Sanukehl Coli
Sinubronchitis,
Swelling,
Fortakehl, Latensin, Mucedokehl, Nigersan,
Mucokehl, Sanuvis
Notakehl
Tennis Elbow,
Sinusitis,
see epicondylitis
Cerivikehl, Luffasan, Mucedokehl, Notakehl,
Pinikehl, Quentakehl, Ruberkehl, Sanukehl Tension Headaches,
Pseu, Sanukehl Staph, Utilin S Muscarsan, Quentakehl, Usneabasan

346
Thromboangiitis obliterans Ulcus cruris,
(Buergers disease), Leptucin, Mucokehl, Notakehl, Sanukehl
Citrokehl, Mucokehl, Nigersan, Notakehl, Myc, Sanukehl Pseu, Sanuvis, Zinkokehl
Sanuvis, Utilin S Upper Abdominal Complaints,
Thrombophlebitis, Fortakehl, Latensin, Mucokehl, Recarcin,
Mucokehl, Notakehl, Sanukehl Myc, Utilin S
Sanuvis, Utilin Urethritis,
Thrombosis, Albicansan, Mucokehl, Nigersan, Notakehl,
Mucokehl, Sanuvis, Utilin, Zinkokehl Pefrakehl, Sanukehl Staph, Sanukehl Myc
Thyroid Disease and Dysfunction, Urinary Tract Infection,
Citrokehl, Fortakehl, Latensin, Mucedokehl, Fortakehl, Latensin, Nigersan, Notakehl,
Nigersan, Pleo Chelate, Recarcin, Sanukehl Pefrakehl, Sanukehl Coll, Sanukehl Myc
Myc, Sanukehl Prot, Sanuvis, Utilin,Utilin S Urticaria,
Tinea, Formasan, Fortakehl, Latensin, Mucokehl,
Pefrakehl, Sanukehl Trich Nigersan, Sanukehl Myc, Sanuvis, Utilin,
Utilin S
Tinnitus,
Citrokehl, Latensin, Leptucin, Mucokehl, Uterine Bleeding,
Nigersan, Notakehl, Sanuvis, Utilin Calvakehl, Ustilakehl
Tonsillitis, Uterine Myoma,
Mucedokehl, Notakehl, Polysan G, Mucokehl, Nigersan, Selenokehl, Utilin S
Sankombi, Sanukehl Staph, Sanukehl Strep, Vaginal Discharge,
Utilin Albicansan, Notakehl, Pefrakehl, Sankombi,
Tooth Abscess, Recarcin, Sanuvis
Arthrokehlan A, Notakehl Vaginitis,
Transient Ischemic Attacks, Albicansan, Grifokehl, Notakehl, Pefrakehl,
Alkala N, Mucokehl, Leptospermusan, Quentakehl, Sanukehl Cand, Sanukehl Coli,
Sanuvis Sanukehl Myc
Trichomycosis (Fungal infection of the Varicose Veins,
hair) and Trichophytosis (Tinea barbae), Mucokehl, Nigersan, Polysan K, Sanuvis
Notakehl, Pefrakehl, Sankombi, Sanukehl Vascular Migraine,
Trich, Utilin S Leptospermusan, Leptucin, Quentakehl,
Trigeminal Neuralgia, Sanoryzae, Selenokehl
Leptospermusan, Stolonikehl, Vitamin B Vascular System Complaints,
Komplex Sanum N Mucokehl
Tubal Cyst, Veins Diseases,
Citrokehl, Mucokehl, Nigersan, Utilin Mucokehl, Polysan K, Sankombi, Zinkokehl
Tubercular Rheumatism, Vertigo,
Bovisan, Citrokehl, Nigersan, Sanum- Luffasan, Mucokehl, Quentakehl
german, Utilin S Vitiligo,
Tuberculoid Skin Problem, Citrokehl, Mucokehl, Nigersan, Sanuvis,
Citrokehl, Nigersan, Polysan T, Utilin, Utilin S
Utilin S Viral Infections,
Tuberculosis in general, Citrokehl, Grifokehl, Leptospermusan,
Bovisan, Chrysocor, Citrokehl, Latensin, Notakehl, Quentakehl, Sanuvis
Nigersan, Polysan T, Sanukehl Myc, Utilin, Vitamin E Deficiency,
Utilin S Mapurit L
Tumors, Vomiting,
see Carcinoma Fortakehl

347
Vomiting of blood, Whooping Cough,
Calvakehl, Fortakehl, Sanukehl Prot see Pertussis
Vulvovaginitis, Wound Healing Problems,
Albicansan, Notakehl, Pefrakehl, Mucokehl, Sankombi, Zinkokehl
Quentakehl, Sanukehl Cand Yeast Infection of the Vagina,
Warts, Albicansan, Alkala N, Citrokehl, Exmykehl,
Citrokehl, Latensin, Quentakehl, Mucokehl, Fortakehl, Pefrakehl, Recarcin, Sanukehl
Nigersan, Sanuvis, Utilin S Cand
Weak Immune System,
see Immunomodulation

348
Notes:

349
Notes:

350
Notes:

351
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352

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