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VACCINE

BREAKTHROUGH
CC HEYWOOD
CC DEPASUCAT
1.4 M children under 5
die of vaccine-
preventable diseases
INTRODUCTION
WHAT ARE VACCINES?
● Biological preparations to
stimulate an individual’s
immune system
● Weakened or killed
pathogens
WHAT DOES A VACCINE DO?
● Prime immune system to recognize and
remember pathogens
● PREVENT spread of infection
● REDUCE severity of illness
● ERADICATE or control deadly diseases
BRIEF HISTORY OF VACCINES Jan 2020 -
SARS-COV 2
Practice of 1900s outbreak
PCECV, and later Dec 2020 -Start
VARIOLATION
rabies for post
SPANISH of vaccine roll-
As protection FLU
from smallpox JENNER exposure out

1796 OUTBREAK

01 02 03 04 05

1400-1700s PASTEUR Y2K


World’s first
People successful 1800s 1945- Influenza
vax
around vaccine 1950s - IPV
the world 1960s - OPV
1974 - EPI
MECHANISM OF VACCINATION

PASSIVE ACTIVE
IMMUNIZATION IMMUNIZATION
Antibody administration from
Stimulates immune system to
a person or an animal to
produce antibodies and cell-
another person to provide
mediated immunity by
temporary protection
immunizing agents.
CLINICAL TRIAL
Pharmaceutical quality and
1 PRECLINICAL non-clinical research

Human pharmacologic studies


2 PHASE 1 in 20-100 healthy volunteers

Therapeutic exploratory studies


3 PHASE 2 in several hundred volunteers

Clinical efficacy and safety


4 PHASE 3 studies in thousands
volunteers
CLINICAL TRIAL
Pharmaceutical quality and
1 PRECLINICAL non-clinical research

Human pharmacologic studies


2 PHASE 1 in 20-100 healthy volunteers

● Animal modelsTherapeutic exploratory studies


3 PHASE 2
● Safety in several hundred volunteers
● Safe dosage

Clinical efficacy and safety


4 PHASE 3 studies in thousands
volunteers
CLINICAL TRIAL
Pharmaceutical quality and
1 PRECLINICAL non-clinical research

Human pharmacologic studies


2 PHASE 1 in 20-100 healthy volunteers

Therapeutic exploratory studies


3 PHASE 2 in several hundred volunteers

Clinical efficacy and safety


4 PHASE 3 studies in thousands
volunteers
CLINICAL TRIAL
Pharmaceutical quality and
1 PRECLINICAL non-clinical research

Human pharmacologic studies


2 PHASE 1 in 20-100 healthy volunteers

Therapeutic exploratory studies


3 PHASE 2 in several hundred volunteers
● Test on HEALTHY human volunteers
● Effectiveness and safeefficacy
Clinical dosageand safety
4 PHASE 3 studies in thousands
volunteers
CLINICAL TRIAL
Pharmaceutical quality and
1 PRECLINICAL non-clinical research

Human pharmacologic studies


2 PHASE 1 in 20-100 healthy volunteers

Therapeutic exploratory studies


3 PHASE 2 in several hundred volunteers

Clinical efficacy and safety


4 PHASE 3 studies in thousands
volunteers
CLINICAL TRIAL
Pharmaceutical quality and
1 PRECLINICAL non-clinical research

Human pharmacologic studies


2 PHASE 1 in 20-100 healthy volunteers

Therapeutic exploratory studies


3 PHASE 2 in several hundred volunteers

● Test on HUNDREDS of HEALTHY


Clinical human
efficacy and safety
4 PHASE 3
volunteers studies in thousands
volunteers and safe dosage
● MEASURES Effectiveness
CLINICAL TRIAL
Pharmaceutical quality and
1 PRECLINICAL non-clinical research

Human pharmacologic studies


2 PHASE 1 in 20-100 healthy volunteers

Therapeutic exploratory studies


3 PHASE 2 in several hundred volunteers

Clinical efficacy and safety


4 PHASE 3 studies in thousands
volunteers
CLINICAL TRIAL
Pharmaceutical quality and
1 PRECLINICAL non-clinical research

● THOUSANDS ofHuman
healthypharmacologic
volunteers studies
2 PHASE 1
● Compared in 20-100 healthy volunteers
to a placebo

Therapeutic exploratory studies


3 PHASE 2 in several hundred volunteers

Clinical efficacy and safety


4 PHASE 3 studies in thousands
volunteers
HERD IMMUNITY
Vaccines given individually can
provide immunity even to those
who are not vaccinated
TYPES OF VACCINES

LIVE ATTENUATED INACTIVATED COMBINATION


VIRUS VACCINES VACCINES
Derived from live antigens Stimulates immune system to Multiple different antigens of
produce the most effective produce antibodies and cell- an organism mixed as a
immune responses mediated immunity by single product to immunize
immunizing agents. against multiple serotypes
ADVERSE REACTIONS FOLLOWING
VACCINATION

LOCAL SYSTEMIC ANAPHYLACTIC

Derived from live antigens Generalized, includes fever, MOST SEVERE


produce the most effective malaise, myalgia, headache,
immune responses and loss of appetite LEAST FREQUENT
Minimized by good screening
TUBERCULOSIS

EXPANDED PROGRAM
POLIOMYELITIS ON IMMUNIZATION DIPHTHERIA
6 Vaccine preventable
diseases

TETANUS MEASLES
PERTUSSIS
Interventions and Strategies
OVERALL GOAL SPECIFIC GOALS

immunize all
REDUCE morbidity
infants/children
and mortality
among children against the most
against vaccine- common vaccine-
preventable diseases preventable diseases.
Interventions and Strategies
SPECIFIC GOALS SPECIFIC GOALS

● eliminate maternal and


● sustain the polio- neonatal tetanus
free status of the ● Control of diphtheria,
Philippines. pertussis, hepatitis b
and German measles.
● Prevent extra
pulmonary
● eliminate measles tuberculosis among
children.
infection
MANDATES

RA no. 10152
Mandatory Infants and Children Health
Immunization Act of 2011

President Benigno Aquino III

Basic immunization for children under 5


including other types that will be determined by
the Secretary of Health.
● WHO-UNICEF Reaching Every District
(RED)
● Improve immunization and reduce drop
outs

REACHING ● Data analysis for


action
EVERY
● Re-establish outreach
BARANGAY (REB) services
STRATEGY (2004) ● Strengthen links
between community
and service
● Supportive supervision
● Maximizing resources
Strategies
Strengthening Vaccine-
Preventable Disease Status of Implementation
Surveillance

● Critical for ALL health facilities


eradication efforts
● Measles and
have at least one staff
indigenous wild trained on REB
polio
● Adequate vaccines,
needles and
syringes
● What are the included vaccines in this
program?

● BCG ● Available vaccines


● Diphtheria ● Hepatitis A
NATIONAL ● Pertussis ● Varicella
● Influenza
IMMUNIZATION ● Tetanus toxoid ● Pneumococcal
PROGRAM OF THE ● Measles ● Typhoid
PHILIPPINES ● Mumps ● HPV
● Rubella
● Poliovirus
● Hemophilus influenzae
Type B
● Hepatitis B
● Rotavirus
EXPANDED PROGRAM ON IMMUNIZATION
SCHEDULE
BCG
Birth
Hepatitis B

DTwP-Hib-Hep B

OPV 6,10,14 weeks

Pneumococcal

Rotavirus 6 and 10th week

Measles 9 months

MMR 12 months
BCG
Bacillus Calmette - Guerin (BCG) Vaccine

Type of Vaccine ● Live Bacteria


● 1 dose
Number of Doses ● At birth preferably within 2 months of life
Schedule
Dosage ● 0.05ml <12 months and 0.1 ml if ≥ 12 months
● Outer upper arm below deltoid muscle
Injection Site/ Type ● Intradermal
Storage ● Stored between 2-8 C
● Known HIV, TB or other immunodeficiencies
Contraindications ○ Congenital TB, close contact to known or suspected
Adverse Reactions infectious cases, or clinical findings suggestive of TB
● Local abscess, regional lymphadenopathies
Hepatitis B (HepB) Vaccine
● Recombinant DNA
Type of Vaccine ● 2-3 doses
Number of Doses ● At birth for infants ≥ 2kgs within 24 hours of life
● Second dose 1-2 months of age (third dose needed if last dose
Schedule was given at age <24 weeks

Dosage ● 0.5 ml
● Infants: outer mid-thigh; Children and Adults: outer upper arm
Injection Site/ Type ● Intramuscular
Storage ● Stored between 2-8 C

Contraindications ● Anaphylactic reaction- extremely rare


● Local tenderness and redness
Adverse Reactions
Disease Agent Reservoir Spread Duration of Risk Factors
Immunity for Infection
post-
infection
Diphtheria Corynebacterium Humans Close Usually crowding
diphtheria respiratory lifelong
contact or
contact with
infectious
material

Pertussis Bordetella Humans Close No concrete crowding


Pertussis respiratory evidence
contact
Disease Agent Reservoir Spread Duration of Risk Factors
Immunity for Infection
post-
infection
Tetanus Toxin Soil Spores enter None Untreated
producing Animal the body via wounds
Clostridium intestines open especially
Tetani wounds those
caused by
rusty metal,
and
exposure to
animal feces

Maternal Toxin Human Infection None Lack of


Tetanus producing mother through the clean and
Clostridium umbilical safe delivery
Tetani cord in
newborns
Diphtheria, Tetanus, Pertussis Vaccine (DTP)

Type of Vaccine ● Usually part of the pentavalent vaccine


● 3 dose
Number of Doses At minimum age of 6 weeks with intervals of 4 weeks per dose

Schedule (6 weeks, 10 weeks, 14 weeks)

Dosage ● 0.5ml
● Right outer upper thigh
Injection Site/ Type ● Intramuscular
Storage ● Stored between 2-8 C

Contraindications ● Anaphylaxis or hypersensitivity after previous dose


● Mild local and systemic reactions are common
Adverse Reactions
Disease Agent Reservoir Spread Duration of Risk Factors
Immunity for Infection
post-
infection

Meningitis Haemophilus humans Close Usually Overcrowding


and influenzae type respiratory lifelong leading to
pneumonia b bacterium contact exposure
Haemophilus Influenzae Type B Conjugate Vaccine
Type of Vaccine ●

Usually part of the pentavalent vaccine
3 dose
Number of Doses ● At minimum age of 6 weeks with intervals of 4 weeks per dose
(6 weeks, 10 weeks, 14 weeks)
Schedule ● Booster dose- 12-15 months with interval of 6 months from the
third dose

Dosage ● 0.5ml
● Right outer upper thigh
Injection Site/ Type ● Intramuscular
Storage ● Stored between 2-8 C

Contraindications ● Anaphylaxis or hypersensitivity after previous dose


● Mild local and systemic reactions are common
Adverse Reactions
Poliovirus Vaccine
● Inactivated Polio Vaccine (IPV)
Type of Vaccine ● 3 doses- primary series
Number of Doses ● At minimum age of 6 weeks with intervals of 4 weeks per dose
● First booster at 12-18 months with interval of 6 months from
Schedule the third dose of primary series
● Second booster at 4-6 years old (if 4th dose given at 4 years
old or onward no second booster is needed)

Dosage ● 0.5ml
● Intramuscular- or in combination with DPT- containing vaccines
Injection Site/ Type ● Stored between 2-8 C
Storage
Previously unvaccinated ● 3 doses given
○ First two doses 4 weeks apart
at ages 7-11 months ○ Third dose is given after 2 months from the second dose
ideally at or after the first birthday
Poliovirus Vaccine- OPV/ IPV
● National Immunization Program (DOH)
○ Oral Polio Vaccine (OPV)
■ 3 doses; 4 week intervals
■ 6 weeks, 10 weeks, 14 weeks
○ Inactivated Polio Vaccine (IPV)
■ 2 doses
● First dose IPV given together with 3rd dose of OPV
● Second dose at 9 months with measles vaccine
Pneumococcal Conjugate Vaccine
● Pneumococcal Polysaccharide and Pneumococcal Conjugate
Type of Vaccine ● PCV- 3 doses; PPV- 1 dose
Number of Doses ● At minimum age of 6 weeks with intervals of 4 weeks per dose
● Booster dose 6 months from the third dose of primary series
Schedule

Dosage ● 0.5ml
● Anterolateral (outer) part of the left thigh (vastus lateralis) for infants,
Injection Site/ Type upper arm (deltoid) for adults
Storage ● Intramuscular- or in combination with DPT- containing vaccines
● Stored between 2-8 C
Previously ● 3 doses given
○ First two doses 4 weeks apart
unvaccinated at ages 7- ○ Third dose is given after 2 months from the second dose
11 months ideally at or after the first birthday
Pneumococcal conjugate Vaccine
● PCV 10: 1-5 years old
Previously ○ 2 doses at least 2 months apart
unvaccinated older ● PCV 13: 12-23 months
○ 2 doses at least 2 months apart
children ages 12 ● 2- 5 years old patient give 1 dose
months - 5 years
Rotavirus Vaccine
● Live attenuated virus, oral
Type of Vaccine ● 2 doses (Rotarix- RV1); 3 doses (Rotateq- RV5);
Number of Doses ● RV1- minimum 6 weeks with 4 week interval minimum
● Oral liquid formulation of RV5- 6-12 weeks, with minimum of 4-
Schedule 10 weeks interval; last dose not given beyond 32 weeks old
● Oral freeze-dried formulation of RV5- 2,4,6 months given at
minimum age of 6 weeks with 4 week intervals; last dose
should not be given beyond 12 months of age

Dosage ● 1ml
● Oral
Injection Site/ Type ● Stored between 2-8 C
Storage
● Severe allergic reaction to previous dose, immunodeficiency,
Contraindications history of malformation of the GI tract
Adverse Reactions ● Mild: irritability in patient, ear infection, diarrhea, vomiting,
runny nose; Severe: intussusception
Disease Agent Reservoir Spread Duration of Risk Factors
Immunity for Infection
post-
infection

Influenza Virus Humans Close Weak Overcrowding


respiratory immunity leading to
contact and exposure
airborne
droplet
Influenza Vaccine (Trivalent/ Quadrivalent)
Type of Vaccine ●

Trivalent and Quadrivalent
Given at a minimum of 6 months age
Number of Doses ● Children 6 months- 8 years receiving first dose should have 2
doses with intervals of 4 weeks
Schedule ● If only one dose given during previous influenza season:
○ 2 doses given followed by 1 dose a year after
● Children 9-18 years
○ 1 dose yearly; usually during February
Dosage ● Dose varies as per manufacturer recommendation
● Trivalent given intramuscularly or subcutaneously; Quadrivalent
Injection Site/ Type given intramuscularly
Storage ● Stored between 2-8 C

Contraindications ● Severe allergic reaction to previous dose, moderate to severe


illness, and those with history of Guillain- Barre Syndrome
Adverse Reactions following a previous dose of vaccine
MEASLES

Type of Vaccine ● Live attenuated


● 1 dose
Number of Doses ● At 9 months
Schedule ○ 6 months in case of outbreaks

Dosage ● 0.5ml
● Anterolateral thigh
Injection Site/ Type ● Subcutaneously
Storage ● Stored between 2-8 C

● MMR/MR given as substitute for infants below 12 months


If monovalent ○ In these cases→ 2 more MMR vaccines received starting
unavailable at 1 year old
Measles- Mumps- Rubella Vaccine (MMR)
● Live attenuated
Type of Vaccine ● 2 doses
Number of Doses ● At minimum age of 12 months
● Second dose at 4-6 years of age or earlier but with a minimum
Schedule of 4 weeks interval

Dosage ● 0.5ml
● Anterolateral thigh
Injection Site/ Type ● Subcutaneously
Storage ● Stored between 2-8 C

● Known allergies, pregnancy, immunodeficiency


Contraindications ● Mild: fever, rash, 5-12 days after immunization
Adverse Reactions ● Severe: thrombocytopenia, anaphylaxis, encephalitis; joint pain
in older women; parotitis with mumps
Measles- Mumps- Rubella- Varicella Vaccine
● Live attenuated
Type of Vaccine ● 2 doses
Number of Doses ● At minimum age of 12 months and maximum age 12 years
● Alternative to MMR and Varicella vaccines given separately
Schedule ● Recommended minimum interval between doses is 3 months,
though second dose given 4 weeks from first dose is valid

Dosage ● 0.5ml
● Anterolateral thigh
Injection Site/ Type ● Subcutaneously
Storage ● Stored between 2-8 C
Varicella Vaccine
● Live attenuated
Type of Vaccine ● 2 doses
Number of Doses ● At minimum age of 12 months
● Second dose given 4-6 years of age but may be given earlier
Schedule with interval of 3 months from first dose
○ (if dose given 4 weeks from first dose still valid)
● Children 13 years or older: dose interval 4 weeks

Dosage ● 0.5ml
● Anterolateral thigh
Injection Site/ Type ● Subcutaneously
Storage ● Stored between 2-8 C
Japanese Encephalitis Vaccine
● Live attenuated recombinant vaccine
Type of Vaccine ● 1 dose
Number of Doses ● Given at minimum of 9 months old
● Those 9 months- 17 years receive primary dose followed by
Schedule booster 12-24 months after
● 18 years+ - single dose

Dosage ● 0.5ml
● Outer upper arm
Injection Site/ Type ● Subcutaneous
Storage ● Stored between 2-8 C

● Allergy to vaccine, pregnancy, immunodeficient conditions,


Contraindications acute and severe chronic diseases with symptoms of fever.
Adverse Reactions Encephalopathy, or uncontrolled epilepsy
● High fever, injection site reactions, low grade fever, irritability,
nausea, and dizziness.
Hepatitis A Vaccine (HAV)

Type of Vaccine ● Live attenuated Vaccine and Inactivated Hepatitis Vaccine


● 1 dose and 2 doses respectively
Number of Doses ● 18 months minimum and 12 months minimum respectively
Schedule ● Inactivated doses must have minimum interval of 6 months
● Inactivated Hepatitis A vaccine- given intramuscularly
Dosage ● Live attenuated vaccine- given subcutaneously

● Both: severe allergic reaction to vaccine component and


Contraindications moderate to severe illnesses
● Live: immunosuppression, pregnancy and recent receipt of
blood products
Human Papillomavirus Vaccine (HPV)
● Bivalent (2vHPV), Quadrivalent (4vHPV), and Nonavalent
Type of Vaccine (9vHPV)
Number of Doses/ ● Ages:
○ 9-14 years 2 doses recommended (0, 6 months)
Schedule ■ First dose and second dose with 6 month interval
■ If first two dose interval is less than 6 months a
third dose is needed 3 months after second dose
○ 15 years and older: 3 doses (0,2,6 months)
■ First and second dose minimum interval is 1 month
■ Second and third dose interval is 3 months
○ Males 9-18 4vHPV and 9vHPV given to help prevent
anogenital warts and anal cancer
● Outer upper arm below deltoid muscle or anterolateral aspect
Injection Site/ Type of the thigh
Storage ● Intramuscular
● Stored between 2-8 C
VACCINES FOR
SPECIAL
GROUPS/
HIGH RISK
Pneumococcal conjugate Vaccine (PCV)/ Pneumococcal
Polysaccharide Vaccine (PPSV23)
Given How? PCV or PPSV23?
Depends on age and
If possible, PCV doses
indication
should be prior to
PPSV23
Intramuscularly

Schedule Dose
8 week interval Immunocompromised
individuals should
receive both at separate
times
PCV-PPSV23 Vaccination Schedule Indications for Pneumococcal Vaccines

Age: 24 months to 5 years ONE DOSE


● Administer 1 dose PCV if 3 doses given •Chronic heart disease, including congestive heart
previously; give 1 or 2 doses PPSV23 at failure and cardiomyopathies
least 8 weeks after most recent dose of •Chronic lung disease, including chronic obstructive
PCV pulmonary disease, emphysema, and asthma
•Diabetes mellitus, Cerebrospinal fluid leaks,
● Administer 2 doses of PCV 8 weeks apart
Cochlear implant(s), Alcoholism
if unvaccinated or less than 3 doses PCV
•Chronic liver disease
was given precious; give 1 or 2 doses of
PPSV23 at least 8 weeks after most TWO DOSES
recent dose of PCV •Sickle cell disease and other hemoglobinopathies
•Congenital or acquired asplenia, or splenic
Age: 6-18 years dysfunction
● Administer 1 dose of PCV13 if no •HIV infection
precious doses; give 1 or 2 doses of •Chronic renal failure and nephrotic syndrome
PPSV23 at least 8 weeks after the most •Diseases associated with treatment with
recent dose immunosuppressive drugs or radiation therapy
•Congenital or acquired immunodeficiency
•Hodgkin disease
•Solid organ transplant
Anti-rabies Vaccinations

● For immunocompetent individuals given WHO prequalified vaccines (Verorab ® or Rabipur®):


○ Intramuscular(IM) regimen: Purified Vero Cell Rabies vaccine (PVRV) 0.5 ml OR
○ Purified Chick Embryo Cell vaccine (PCECV) 1 ml given on days 0 and 7
○ Intradermal (ID) regimen: PVRV or PCECV 0.1 ml given on days 0 and 7
● For immunocompromised individuals or those given non-WHO prequalified vaccines, give 3 doses on days 0, 7, 21 or
28
● A repeat dose should be given if the vaccine is inadvertently given subcutaneously
● Never give in the gluteal area
● In the event of subsequent exposures:
○ High-risk* individuals who have completed PrEP require booster doses, regardless of the interval between
exposure and last dose of the vaccine.
○ Booster doses may be given through either:
■ 1-visit regimen: 0.1 ml ID (PVRV or PCECV) on each of the 4 sites on day 0
■ 2-visit regimen: 0.1 ml ID (PVRV or PCECV) OR 0.5 ml PVRV or 1.0 ml PCECV IM at 1 site on days 0 and
3
Meningococcal Vaccine
• 0.5 ml Given intramuscularly (IM) or subcutaneously (SC)
• Tetravalent meningococcal conjugate vaccine MCV4-D, MCV4-TT, MCV4-CRM given intramuscularly (IM)
• Tetravalent meningococcal polysaccharide vaccine (MPSV4) given intramuscularly (IM)/subcutaneously (SC)

Indications in :
● Persistent complement component deficiencies
● Anatomic/functional asplenia (including sickle cell disease)
● HIV
● Travelers to or resident of areas where meningococcal disease is hyperendemic or epidemic

Schedule:
● MCV4-D: minimum age is 9 months
● 9-23 months old: 2 doses 3 months apart
● 2 years and above give one dose
○ Except in cases of asplenia, HIV, persistent complement component deficiency where 2 doses given 8 weeks apart
Meningococcal Vaccine

Schedule:
● MCV4-TT: minimum age is 6 weeks
○ 6-12 weeks old: give first 2 doses at least 2 months apart; the 3rd (booster) dose is at age 12 months
○ 12 months of age to adolescence: 1 dose only
● MCV4-CRM: given to children 2 years and above as a single dose
○ Revaccinate with a MCV4 vaccine every 5 years
● RABIES VACCINE MENINGOCOCCAL VACCINES Polysaccharide vaccines (MPSV4)
○ Given to children 2 years and above as a single dose followed by MCV4 as a second dose 2 months after
○ Booster doses of MPSV4 are not recommended.
Haemophilus Influenzae Type B
Conjugate Vaccine
● Given intramuscularly (IM)
● Indications for children with:
○ Chemotherapy recipients, anatomic/functional asplenia including sickle cell disease, HIV infection,
immunoglobulin or early component complement deficiency
● Age 12-59 months:
○ Unimmunized* or with one Hib vaccine dose received before age 12 months, give 2 additional
doses 8 weeks apart
○ With ≥ 2 Hib vaccine doses received before age 12 months., give 1 additional dose
Haemophilus Influenzae Type B
Conjugate Vaccine
● For children ≤ 5 years old who received a Hib vaccine dose(s) during or within 14 days of starting
chemotherapy or radiation treatment, repeat the dose(s) of Hib vaccine at least 3 months after
completion of therapy
● For children who are hematopoietic stem cell transplant recipients, revaccination with 3 doses of Hib
vaccine given 4 weeks apart, starting 6-12 months after transplant, is recommended regardless of
vaccination history.

● Unimmunized and ≥ 15 months of age to undergo elective splenectomy should be given 1 dose of Hib-
containing vaccine at least 14 days before the procedure
● Unimmunized 5-18 years old and with either anatomic or functional asplenia (including sickle cell
disease) or HIV infection, should be given 1 dose of Hib vaccine
Typhoid Vaccine

● Given intramuscularly (IM)


● Given at a minimum age of 2 years old with revaccination every 2—3
years
● Recommended for travelers to areas where there is a risk for exposure
and for outbreak situations as declared by public health authorities
Cholera Vaccine
• Given per orem (PO)
• Given at a minimum age of 12 months as a 2-dose series two weeks apart.
• Recommended for outbreak situations and natural disasters as declared by health
authorities
Hepatitis A Vaccine

Given intramuscularly (IM)


● Administer 2 doses of Hepatitis A vaccine, at least 6 months apart
to unvaccinated individuals who are at increased risk for infection:
○ Travelers to or are working in countries with intermediate or
high endemicity of infection
○ MSMs, Homelessness, Users of injection and non-injection
illicit drugs,
○ Working with HAV infected primates or with HAV in research
laboratories, o With clotting factor disorders, and chronic liver
disease o HIV
Human Papillomavirus Vaccine
Given intramuscularly (IM)
● Give 3 doses of HPV vaccine following the 0, 1-2, and 6 month schedule, regardless
of age at vaccine initiation to the following:
○ Children with history of sexual abuse or assault starting at age 9 years
○ Immunocompromised children

● Pregnancy- not recommended


■ If given during pregnancy, delay the remaining doses until after
pregnancy. Pregnancy testing is not necessary before initiating HPV
vaccination
Adult
Vaccinations
COVID 19 VACCINE

● 0.5 ml, IM, 2 doses, 21 days apart


BNT162b2
(Pfizer/BioNTech)
● 0.5 ml, IM, 2 doses, at least 28 days
mRNA-1273 (Moderna) apart

● 0.5 ml, IM, 2 doses, at least 12 weeks


ChAdOx1 (AstraZeneca) apart
COVID 19 VACCINE

Gam-COVID-Vac (Gamaleya) ● 0.5 ml, IM, 2 doses, 21 days apart

Ad26.COV2.S ● 0.5 ml, IM, single dose

(Janssen/Johnson&Johnson)

● 0.5 ml, IM, 2 doses, at least 28 days


Coronavac (Sinovac) apart
COVID-19 VACCINE

THE CDC RECOMMENDS AGAINST THE USE OF THE FOLLOWING


VACCINES IN YOUNGER CHILDREN:

BNT162b2: <16 years old


ChAdOx1: <18 years old
MYTHS AND FACTS
CAN A COVID-19 VACCINE MAKE ME SICK WITH COVID-19?

No. None of the authorized and recommended COVID-19 vaccines or COVID-19


vaccines currently in development contain the live virus that causes COVID-19. This
means that a COVID-19 vaccine cannot make you sick with COVID-19.

WILL A COVID-19 VACCINE ALTER MY DNA?

No. COVID-19 vaccines do not change or interact with your DNA in any way.There are
currently two types of COVID-19 vaccines that have been authorized for use in the
United States: messenger RNA (mRNA) vaccines and viral vector vaccines.
MYTHS AND FACTS
WILL A VACCINATION PROTECT ME FROM GETTING SICK WITH COVID-19?

Yes. COVID-19 vaccination is like teaching your immune system how to recognize the
virus that causes COVID-19 and how to fight it. As a consequence, this protects you
from getting sick with COVID-19.

IF I'VE ALREADY HAD COVID-19, DO I STILL NEED TO GET VACCINATED?

Yes. It is recommended that you should be vaccinated regardless of whether you


already had COVID-19. Since it is not yet known how long you are protected from
getting sick again after recovering from COVID-19, you should get vaccinated.
INFLUENZA VIRUS
Type of Vaccine ●

Inactivated Trivalent or Quadrivalent
Covers AH1N1, AH3N2, 1 Influenza virus
Indications (2 for Quadrivalent), prevailing WHO
recommendation
● May be given to cancer and PLHIV px to
prevent pneumonia associated mortality

Dosage and schedule ●



Yearly
IM, deltoid
Injection Site/ Type
Adverse Reactions ●

Local
Known anaphylactics, especially previous
Contraindications vaccine components
TETANUS, DIPHTHERIA, PERTUSSIS
Type of Vaccine ● Fixed combinations of tetanus and
diphtheria toxoids, and accellular
Indications pertussis
● Immunity after pediatric dose wanes after
5-10 years
● Given to pregnant women 2 doses with 4
week intervals

Dosage and schedule ● At least the same amount of toxoid in


pediatric doses but a reduced amount of
Injection Site/ Type diphtheria toxoid (20:2 IU)
● Second dose given 4-8 weeks after first
dose
● Third dose after 6-12 months
● IM, deltoid

● Local
MEASLES, MUMPS, RUBELLA
Type of Vaccine ●

Inactivated Trivalent or Quadrivalent
Covers AH1N1, AH3N2, 1 Influenza virus
Indications (2 for Quadrivalent), prevailing WHO
recommendation
● May be given to cancer and PLHIV px to
prevent pneumonia associated mortality

Dosage and schedule ●



Yearly
IM, deltoid
Injection Site/ Type
Adverse Reactions ●

Local
Known anaphylactics, especially previous
Contraindications vaccine components
VARICELLA
Type of Vaccine ● Pneumococcal Polysaccharide Vaccine
(PPSV23) and Pneumococcal Conjugate
Indications Vaccine (PCV13)
● Immunocompetent adults, and elderly
(>60) to prevent pneumococcal
pneumonia

Dosage and schedule ●



2 doses 4 to 8 weeks apart
IM
Injection Site/ Type
Adverse Reactions ●

Local
Known anaphylactics
Contraindications
ZOSTER RECOMBINANT (RZV)
Type of Vaccine ●

Live attenuated
Adjuvanted recombinant
Indications ● >60 w/o prior history for disease
prevention
● If w/ history, for preventing recurrence

Dosage and schedule ●



Single dose for Live attenuated
Two doses (0.5ml) for recombinant
Injection Site/ Type ● IM, deltoid
● 2-6 months apart

Adverse Reactions ● Local, shivering, and gastrointestinal


symptoms may occur
Contraindications ● Known anaphylactics, especially vaccine
components and neomycin
HUMAN PAPILLOMAVIRUS
Type of Vaccine ●

Bivalent, Quadrivalent, Nonavalent
Immunocompetent women given until 26
Indications years old

Dosage and schedule ●



0-1-6 months for bivalent
0-2-6 months for quadrivalent and
Injection Site/ Type nonavalent
● IM, deltoid

Adverse Reactions ●

Local, dizziness
Known anaphylactics, especially previous
Contraindications vaccine components and yeast
● NO studies on the effect of nonavalent
vaccines on males
HUMAN PAPILLOMAVIRUS
Type of Vaccine
Indications
Dosage and schedule
Injection Site/ Type
Adverse Reactions
Contraindications
PNEUMOCOCCAL VACCINE (PCV)
Type of Vaccine ● Pneumococcal Polysaccharide Vaccine
(PPSV23) and Pneumococcal Conjugate
Indications Vaccine (PCV13)
● Immunocompetent adults, and elderly
(>60) to prevent pneumococcal
pneumonia

Dosage and schedule ●



0.5 ml SC or IM
PCV13 as first dose, followed by PPSV23
Injection Site/ Type a year later, no revaccination needed
● >50 yo given PPSV23 may be given PCV
13 at least 1 year later

Adverse Reactions ●

Local
Known anaphylactics, especially previous
Contraindications vaccine components and yeast
● PPSV23 can be given during pregnancy
HEPATITIS A
Type of Vaccine ● Formalin-inactivated monovalent,
adsorbed aluminum hydroxide as
Indications adjuvant
● Adult immunocompetent, Men having sex
with men, hemophiliacs, contacts of
infected persons, endemic to a region

Dosage and schedule ● 2 doses, 0- (6-12) months, 1440 ELISA


units per ml
Injection Site/ Type ● IM, deltoid

Adverse Reactions ●

Local
Known anaphylactics, especially previous
Contraindications vaccine components
● Administer with caution to those with
bleeding disorders
HEPATITIS B
Type of Vaccine ● Monovalent recombinant Hepatitis B or Combined inactivated
Hepatitis A and B
Number of Doses ● 0-1-6 months to confer immunity
● 0-2-6 weeks for High Risk Individuals [ACCELERATED]
Schedule ○ 1 booster dose 1 year after 1st dose if titers are below 10
mIU/ml, after 5 years for healthy individuals

● 0.5ml, IM, Deltoid


Dosage
Injection Site/ Type

Adverse Reactions ● Pain, redness, soreness at injection site, and fever


● Hypersensitivity especially to yeast, those with moderate or
Contraindications severe illness
● NO STUDIES on effects to breastfeeding mothers and infants
MENINGOCOCCAL
Type of Vaccine ● Quadrivalent polysaccharide from
serotypes A, C, Y, W-135
Indications ● Routine administration is NOT
recommended in immunocompetent
● 65 and above, travelling to endemic areas

Dosage and schedule ●



0.5 ml, single dose 10 days before travel
2 doses 2 months apart
Injection Site/ Type ● Re-vaccinate with 2 doses ever 5 years
● IM, deltoid

Adverse Reactions ●

Local
Known anaphylactics, especially previous
Contraindications vaccine components
HAEMOPHILUS INFLUENZAE B
Type of Vaccine ● Conjugated polysaccharides with: DPT
carrier proteins and N. meningitidis type
Indications B outer membrane protein complex

Dosage and schedule ● Single dose of pediatric vaccine IM

Injection Site/ Type


Adverse Reactions ●

Local
Known anaphylactics, especially previous
Contraindications vaccine components, neomycin, and
gelatin
● PREGNANT WOMEN
VACCINE HESITANCY

TOP 10 GREATEST THREAT TO PUBLIC HEALTH (WHO, 2019)


Delay or rejection of vaccines in spite availability
● Pseudoscience
● False claims

Outcomes of vaccine hesitancy


● Decrease in demand
● Decreased coverage of both childhood and adult vaccination
● Increased vaccine-preventable disease outbreaks and epidemics
VACCINE HESITANCY

TOP 10 GREATEST THREAT TO PUBLIC HEALTH (WHO, 2019)


Delay or rejection of vaccines in spite availability
● Pseudoscience
● False claims

Outcomes of vaccine hesitancy


● Decrease in demand
● Decreased coverage of both childhood and adult vaccination
● Increased vaccine-preventable disease outbreaks and epidemics
VACCINE HESITANCY

HOW TO PREVENT VACCINE OPPOSITION


● STRENGHT OF RECOMMENDATION
● TAILORED COMMUNICATION
● TRANSPARENCY AND ACCURACY
● SUPPORT FROM ACCESIBLE AND RELIABLE INFORMATION
● REINFORCEMENT OF VACCINE RECCOMENDATIONS

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