Professional Documents
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DANGEROUS DRUGS
DEFINITION OF TERMS
Drugs – natural or synthetic substance that is used to produce physiological or psychological effects
in humans or other higher order animals within a short period of time after ingestion of a specified
dose.
Dangerous Drugs – has a low therapeutic margin of safety (e.g. the amount of medication to help
and the dose that causes death is not large) typically have more serious side effects and greater
risks.
Prohibited Drugs – are not to be sold or used by anybody without special permission; also called
illegal or illicit drugs
Regulated Drug – one of the many types of medication that is used to treat or cure a disease or illness
that is regulated by and has met the standards set by the Food and Drug Administration (FDA).
Drug Abuse – the use of illegal drugs, or the misuse of prescription or over-the-counter drugs for at
least a year with negative consequences.
Drug Syndicate – any organized group of two or more persons forming or joining together with the
intention of committing any offense.
Instrument – anything that is used in or intended to be used in any manner in the commission of illegal
drug trafficking or related offenses.
Laboratory Equipment – the paraphernalia, apparatus, materials or appliances when used, intended
for use or designed for use in the manufacture of any dangerous drug and/or controlled precursor
and essential chemical.
Pharmacology – the branch of medicine concerned with the uses, effects, and modes of action of
drugs.
Trading – transactions involving the illegal trafficking of dangerous drugs and/or controlled precursors
and essential chemicals using electronic devices such as, but not limited to, text messages, email,
mobile or landlines, two-way radios, internet, instant messengers and chat rooms or acting as a
broker in any of such transactions whether for money or any other consideration.
PDEA Philippine Drug Enforcement Agency
(Filipino: Kawanihan ng Pilipinas Laban sa Droga) is the lead anti-drugs law enforcement
agency, responsible for preventing, investigating and combating any dangerous drugs,
controlled precursors and essential chemicals within the Philippines.
The implementing arm of the Dangerous Drugs Board (DDB), is the policy-making and strategy-
formulating body in the planning and formulation of policies and programs on drug prevention
and control.
PDEA and DDB are both under the supervision of the Office of the President.
DRUG DYNAMICS
Drug works because they physically resemble the chemicals naturally produced with in the
body
Drugs affect our physical functions by mimicking these natural chemicals in our body. (e.g.
painkillers resemble endorphins)
DRUG ADDICTION – Continued use of drugs despite knowledge of the harm that it causes yourself
and others (deterioration in work performance, relationships, and social interaction)
SIGNS OF ADDICTION
Four Common Symptoms:
1. Compulsion – excessive need to perform the behavior of obsession
2. Loss of Control – the inability to predict reliability whether any isolated occurrence of
the behavior will be healthy or damaging
3. Negative Consequence – physical damage, legal trouble, financial problems,
academic failure, or family dissolution
4. Denial – the inability to perceive that the behavior is self-destructive
Opium – narcotic drug produced from the drying resin of unripe capsules of the opium poppy.
The green seed heads are cut to release milky latex which contains morphine. This
latex dries on the seed head to form a gum, which is then collected and bulked as raw opium.
Form/Use:
- Granulated
- Powdered
- Tincture (solution)
- Used for GIT pain and diarrhea for infants
Method of Intake: Oral or Smoking
Effects:
General:
Pale/Emaciated appearance Euphoria
Drowsiness Secretiveness
Loss of Appetite Neglect of sex life
Lack of Sleep Possession of Paraphernalia
Neglect of Personal Hygiene
Withdrawal:
Anxiety Running nose Excessive yawning
Depression Nausea Convulsion
Tremors Insomnia Loss of Appetite
Cramps Vomiting Waves of gooseflesh
Watery eyes Diarrhea
a. Morphine
“Morpheus” – Greek word
The primary active drug in opium. It comes in white crystalline powder, light porous cubes
of small white tablets.
Major sedative and pain relieving drug found in opium, being approximately 10% of the
crude opium exudates.
A bitter alkaloid, the soluble salts of which are used in medicine as analgesic, a light
anesthetic or a sedative.
b. Codeine
Second most abundant component of opium, used as a strong painkiller and cough
suppressant (antitussive)
c. Heroin
Sometimes known as “Chinese Heroin”
White powder (from South East Asia) that consists of diamorphine hydrochloride and minor
amounts of other opium alkaloids.
Heroin from South West Asia is much cruder product (brown powder) that contains
diamorphine base, variable amounts of other opium-derived alkaloids as well as
adulterants.
Heroin is a highly addictive drug. Prolonged use also gives rise to drug tolerance, resulting
in higher levels of drug intake required to gain the same pleasurable effects.
2. STIMULANTS
- Are taken to make one feel more energetic, strong or awake (referred as uppers; reverse
the effects of fatigue from both mental and physical tasks)
- When used in moderation, these substances tend to relieve malaise and increase alertness
- Abuse stimulants: Amphetamine, Methamphetamine, and Cocaine
Amphetamine Methamphetamine
- Normally produced as - Produced as methamphetamine
amphetamine sulfate, hydrochloride hydrochloride
or phosphate - More popular in North America and
- Commonly abused in Europe Japan
Clinical Symptoms
- CNS and respiratory stimulation and parasympathetic activity.
- Pyschic stimulation and excitability: temporary increase in mental and physical
activity and nervousness
Acute Toxicity
- Cardiovascular: flushing or pallor, tachypnea, palpitation, tremor, cardiac
arrhythmias
- Mental disturbances: delirium, confusion, delusions and hallucinations
- Acute psychotic syndromes: vivid auditory and visual hallucinations, paranoid
ideation
- Frequent and potential sign: hyperpyrexia
Chronic Usage
- Emotional lability, somnolence, loss of appetite, occupational deterioration, mental
impairment and social withdrawal
- Trauma and ulcer of the tongue and lip
- Paranoid schizophrenia
b. Cocaine
A naturally occurring alkaloid found in certain varieties of plants of the genus
Erythroxylum (coca leaves)
A local anesthetic, vasoconstrictor and powerful psychostimulant
“Crack Cocaine” – base form of cocaine; more prevalent in the recent years
- Prepared from cocaine hydrochloride using baking soda and water
- More granular texture than the salt form, often occurring as “rocks” with slightly
waxy appearance.
Street Names: Coke, crack, gold dust, heaven’s dust, stardust, white girl,
speedballs (when mixed with heroin)
Method of Intake:
- Orally by mixing cocaine with liquid or semi-liquid, then placed in a capsule
- Directly applied to the gums, underneath the tongue or side of the eyelid
- To prevent premature climax, some males apply it directly to the penis & the
females under the vagina
- Injection
- Sniffing/Snorting
Effects:
General: Sensation of mental and physical stimulation, Euphoria, Self-satisfaction & comfort
of the mind and body, Forgetfulness, Desire for sexual activities, Feeling of rejection,
Extreme depression (suicidal tendencies), Psychological dependence
Physical: Sense of smell intensifies, Loss of perception as to time and distance, Constipation,
Dryness of mouth, Insomnia
Immediate: Dilated pupils, Hypertension, Increased heart rate & body temperature,
Heightened sense of awareness, Feeling of being energetic & alert, Loss of appetite,
Slurred speech
*effects are seen within a few minutes, peak in 15-20 minutes and disappear
within an hour
Dangers: Low dose may create psychological problems; overdose may cause delirium,
convulsions, respiratory failure and eventually death. Regular intake of high doses may
cause paranoia or may lead to “cocaine psychosis” (hallucinations); may expose the
user to death from fire or explosion that can occur from preparation of free base.
3. HALLUCINOGENS
- Cause significantly altered mental state, often including hallucinations
- Marijuana is one of the oldest
a. Phencylidine (PCP)
Synthesized in the early 1900s and tested during the World War I as a surgical anesthetic
Discontinued for human use due to the side-effects: Delirium, Paranoia, Hallucinations
and Euphoria
c. Marijuana (Cannabis)
Oldest and most widely used mind-altering drug
Cut, dried and ground hemp plant: Cannabis sativa (rich in cannabinoids, a
psychoactive)
Major psychoactive agent: Delta-9-tetrahydrocannabinol
Hashish – cannabis resin made from the flowering tops of the plant
Hash oil: extract of cannabis resin and contains up to 60% of cannabinoids
*Hash oil can be mixed with tobacco or other vegetable material
Metabolites of Marijuana:
Delta 9 Carboxy-tetrahydrocannabinol
III-hydroxy-delta-9-THC
*Detectable in urine from 1-4 weeks after last injection
d. Dimethyltryptamine (DMT)
A naturally occurring psychedelic compound
When ingested, it produces “trips” or hallucinations
Unique for producing remarkably consistent hallucinations. People who take DMT as a
psychedelic drug consistently report clear, detailed visions of encounters with strange
beings in another dimension. Depending on the person’s worldview, the beings are
identified as either aliens or angels/demons. Visions like these also occur with other
psychedelic drugs, but with nowhere near the consistency of DMT.
e. Mescaline
Obtained from the bud the of small, spineless cactus Peyote (Lophophora williamsi)
Also found in certain members of the Fabaceae (bean family)
The top of the cactus above ground, also referred to as the crown, consists of disc-
shaped buttons that are cut from the root and dried. The buttons are generally chewed
or soaked in water to produce an intoxicating liquid
Main active ingredient: Mescaline
f. Magic Mushrooms
Genus Psilocybe, Pscilocybe mexicana mushroom
Other Names: Psychedelic mushrooms, Shrooms
Active components: Psilocin and Psilocybin
Found in dried or fresh mushrooms or as a powder in capsules
Usually taken orally or sometimes brewed into a tea
a. Barbiturates
Physiologically active depressants, resulting in a physical and mental state similar to
alcohol-induced intoxication
Anti-seizure and anti-convulsion
Causes drowsiness, sleepiness
Condensation product of urea and malonic acid
Fat soluble – easily crosses the Blood-brain Barrier
Effects:
Low Doses: Sedation, Drowsiness and Sleep
Higher Doses: Anesthesia
Very High Doses: Stupor, Coma and Death
Toxicity: Depression, Cyanosis, Hypothermia, Hypotension
1) Barbituric Acid
2) Phenobarbital – long-acting; anticonvulsant
3) Amobarbital – intermediate-acting
4) Pentobarbital – short-acting
5) Thiopental – ultra-short-acting; sedative-hypnotic
b. Benzodiazepines
Tranquilizers
Pharmaceutical preparations that contain diazepam, flunitrazepam, nitrazepam,
flurazepam and temazepam
Mediates the effect of gamma-aminobutyric acid (GABA)
Most are rarely prescribed; illicit synthesis is rare
Commonly abused in conjunction with other drugs, particularly opiates or with alcohol
Gained notoriety for its association with “date rape” or drug facilitated sexual assault
Cause hypnotic, anticonvulsant, muscle relaxant and amnesia effects
Uses: Treatment of anxiety, insomnia, agitation, seizures, and muscle spasms
c. Alcohol
Most abused depressant in the world
Standard drink: any drink containing 10g of alcohol
one standard drink always contains the same amount of alcohol
regardless of container size or alcohol type (i.e. beer, wine or spirits)
*One drink is:
- 12 ounces of regular beer
- 8-9 ounces of malt liquor, which has more alcohol than beer
- 5 ounces of wine
- 1 1/2 ounces of distilled spirits like vodka and whiskey
Effects:
Short-term: Nausea, Vomiting, Headaches, Slurred speech, Impaired judgment, Anxiety,
Insomnia, Trouble concentrating, Memory loss, Problems breathing
Intoxication – a limitation of the body’s physical and mental status, ranging from feeling
energized to being unconscious.
Effects:
Causes euphoria, a feeling of empathy, increased energy and tactile sensation
Short-term health risks: Hypertension, Hyperthermia and Dehydration
Long-term: Severe depression due to permanent disruption of serotonin production in the
CNS
b. Gamma-hydroxybutyric Acid and Analogues
A substance endogenously present in the brain
Originally developed as an anesthetic drug and is still used for that purpose in some
countries
Manufactured easily by adding aqueous sodium hydroxide to gamma-butyrolactone
(GBL)
Acts as CNS depressant and hypnotic; chemically related to GABA
Synonyms: Sodium oxybate (Xyrem), Gamma-OH, Somotomax, “GHB” and “Liquid
ecstasy”
Gained notoriety for its use in drug facilitated sexual assault
c. Ketamine
Anesthetic and animal tranquilizer
Causes anterograde amnesia
Used in powdered or liquid form as an anesthetic, usually on animals
Methods of Intake:
- Injected
- Consumed in drinks
- Snorted
- Added to joints or cigarettes
Effects:
Short-term and Long-term: Increased heart rate and blood pressure, Nausea, Vomiting,
Numbness, Depression, Amnesia, Hallucinations and Potentially fatal respiratory
problems.
* Ketamine users can also develop cravings for the drug.
High Doses: Users experience an effect referred to as “K-Hole,” an “out of body” or “near-
death” experience
***Rohypnol, GHB, and Ketamine have implicated in cases of Drug Facilitated Sexual
Assaults (Date-rape Drugs)
6. ATHLETIC PERFORMANCE ENHANCERS
Athletes trying to gain competitive edge may abuse stimulants and painkillers
The first drug controlled because of their abuse by athletes were Anabolic Steroids
a. Anabolic Steroids
Promote cell growth resulting in growth of the muscle tissue and sometimes bone size
and strength
Synthetic, or human-made, variations of the male sex hormone testosterone. The proper
term for these compounds is anabolic-androgenic steroids.
- Androstenedione – marketed as to body builders in dietary supplements and
claimed to have an anabolic effect
Effects:
Pharmacological: Increased heart rates, heart muscle oxygen consumption rate and heart
stroke volume
Psychodynamic: Raised alertness, Euphoria, Sensation of relaxation
Addictive Properties: Highly addictive, Sudden stop of taking nicotine can cause
withdrawal symptoms which includes cravings, a sense of emptiness, anxiety, depression,
moodiness, irritability, and inattentiveness.
*The American Heart Association says that nicotine (from smoking tobacco) is one of the
hardest substances to quit – at least as hard as heroin.
*Vapes do not actually help in cigarette addiction
*Second hand smokers have 14% chance to suffer lung cancer
b. Dextromethorphan (DXM)
Cough and cold medications
E.g. Robitussin
Method of Intake: People who use inhalants breathe in the fumes through their nose or
mouth, usually by “sniffing,” “snorting,” “bagging,” or “huffing”
Effects:
Short-term: Slurred or distorted speech, Lack of coordination (control of body movement),
Euphoria (feeling "high"), Dizziness, sometimes Hallucinations
Long-term: Liver and kidney damage, Hearing loss, Bone marrow damage, Loss of
coordination and limb spasms (from nerve damage), Delayed behavioral development
(from brain problems), Brain damage (from cut-off oxygen flow to the brain)
SCHEDULE OF DRUGS
Includes drugs with no proven or acceptable medical use and a high abuse
potential - authorized research only.
Schedule 1
(Heroin, lysergic acid diethylamide (LSD), marijuana (cannabis), 3,4-
methylenedioxymethamphetamine (ecstasy), methaqualone, and peyote)
Includes narcotic drugs with a high potential for abuse but with currently
accepted medical use in treatment.
Schedule 2
(Opiates, cocaine, methadone, meperidine, oxycodone, morphine,
hydrocodone, fentanyl)
Includes non-narcotic drugs with a high potential for abuse, such as
Schedule 2N amphetamines, phenmetrazine, pentobarbital, methylphenidate, and short-
acting barbiturates.
Includes narcotics in combination with other non-narcotic drugs, such as
Schedule 3
codeine combined with acetaminophen or aspirin, and buprenorphine.
Includes ketamine, anabolic steroids, and central nervous system depressants,
Schedule 3N such as glutethimide, methyprylon, and barbiturates not listed in other
schedules. Also includes anorectant agents not included in other schedules.
Includes narcotics in combination with other non-narcotic drugs,
antidiarrheals, mild CNS depressants, mild CNS stimulants, and tranquilizers.
Schedule 4 Drugs such as chloral hydrate, meprobamate, phenobarbital, diphenoxylate
with atropine sulfate, chlordiazepoxide, diazepam, carisoprodol, midazolam,
alprazolam, and phentermine are in this group.
Includes narcotic cough syrups and ephedrine, pseudoephedrine, and
Schedule 5
phenylpropanolamine products.
REPUBLIC ACT NO. 9165 COMPREHENSIVE DANGEROUS DRUGS ACT OF 2002
June 7, 2002
Repealed RA 6425, otherwise known as the Dangerous Drug Act of 1972
Drug Testing
- Increasing applicability in:
o Government agencies
o Industrial agencies
o Sports agencies
General Information
Urine Specimen – the usual sample used to test a number of drugs of abuse
Requires the highest standard of analytical methodology, specimen security and
documentation
Certification of the laboratory is required
Important to guard against specimen exchange or adulteration
Urine is collected in a tamper proof specimen cup often proportioned into separate
specimens
Positive specimens are to be stored frozen for a minimum of 1 year
Disadvantages of Urine Specimen:
Detects only fairly recent drug use
Will not differentiate casual use from chronic drug abuse
Does not determine degree of impairment to tissues
Does not determine dose of drug taken
Will not state exact time of use
Detection limited to a few days after drug use
Three Ways of Tampering Urine for Drug Testing
Dilution
Adulteration – substances are added to urine that will interfere with drug testing
Substitution – checking the clothing of the client if there are extra vials
*Checking the temperature of the urine sample; fresh urine is warm (32.5°C to 37.7°C)
Screening Test – initial test: to screen urine specimens, to eliminate “negative ones” from
further consideration and identify the presumptively positive specimens that of the initial test to
ensure reliability and accuracy.
Alternative Specimens
Meconium
- First stools of the newborn
- Begins to form during second trimester and continues to accumulate until birth
- Provides evidence of maternal drug use anytime during the last two trimesters
Hair
- Obtained easily
- Not altered or manipulated easily to prevent drug detection
- Prior drug abuse may be detected for several months
- Mechanism of Drug Deposition in Hair:
Transfer from blood to growing hair shaft
Transfer from sweat
Environmental contamination
- Tested through radioimmunoassay
Sweat
- Sweat-patch collection devices, worn for several days to several weeks during
which the drug, if present, accumulates in the absorbent pad in the patch, while
water vapor escapes through the semipermeable covering
- Advantage: monitoring of drug use in correctional institutions or in drug rehab
programs
Saliva
- Easy to obtain, less invasion of privacy and ease of adulteration
- Ultrafiltrate of plasma
- Detection of drug level is shorter compared to urine
- Recent drug use
- Correlates with degree of impairment
- Sweat production: 1.5L/day in average
Laboratory Considerations
1. Specimen Collection
Urine: Sample of choice; represents the net load of the drug over a long period
Guard against exchange, adulteration or tampering
Urine pH is 6.0 in average; Specific gravity = 1.002 – 1.030
Presence of creatinine
Blood: Represents transient passage of the drug thru the circulation
Only a quick picture of the drug level at a specific time
2. Processing and Handling
Confidentiality and Chain of Custody
3. Analytical Methods
Screening Assay – good sensitivity with marginal specificity
Confirmatory Assay – high sensitivity and specificity
– qualitative and quantitative information
– different from screening procedure
Levels of Drug Testing
1. Emergency Room Testing
- Rapid, stat, screening methods
- EMIT, FPIA and TLC
2. Forensic Testing
- Confirmatory testing
- HPLC and GC-MS
B. CHROMATOGRAPHIC METHODS
i. Thin Layer Chromatography
- Use of solid phase support medium and liquid mobile phase separation
system
- Drugs are separated on the basis of their ability to dissolve in the solvent
system and its strength of interaction with the support phase
- Color reactions are then used to locate and identify the specific substance
- Urine sample adjusted to pH 8.5
- Screening for drug identification
ii. High Performance Liquid Chromatography
- Able to separate a variety of different materials fairly rapidly
- Not very specific
iii. Gas Chromatography/Mass Spectrometry
- Most specified and sensitive: Gold Standard
- Parent drug and metabolites may be detected
- Sample is placed in a solvent to extract the substance
- Extract is concentrated and injected into a gas chromatograph
- Fractionation pattern is determined
- Mass Spectrometry: determine molecular weight and structural
characteristics to identify the drug
**HPLC and GC-MS are the confirmatory methods for drug identification
C. SPECTROPHOTOMETRIC
- Based on the absorption of the amount of light by a solution that contains analyte
- Spectral Scan: tentative identification for drugs
- Protein precipitation or extraction
- Quantitative analysis
- E.g. Salicylate: 340-700 nm, Barbiturates: <340 nm (UV), Quinidine: Fluorescent