Rx Item-Recombivax PF 40MCG/ML 1 ML Vial -KEEP REFRIG- by Merck & Co Pharma USA , Clinical Information:
Generic Code And Description: 62677 Hepatitis B Virus Vaccine/Pf Preservative Free Intramuscular Vial 40 Mcg/Ml
Strength: 40 Mcg/Ml
Dose Form: Vial (Ml)
Product Category: : Rx Pharmaceuticals
Fine Line Class: 850085008510 All Rx Products
DEA Class: None Omp Family:
Drug Class: 80120000 Vaccines
Active Ingredients: 8320 Hepatitis B Virus Vaccine Recombinant
9870 Preservative Free
Inactive Ingredients: 8921 Latex Drug Class: Drug Class: 80120000 Vaccines , OMP Family: , Temparature Zone: 30 Refrige./DoNot Freez, Unit Dose Indicator: NO, Item Size: 1ML, Brand Label Flag: BRAND , Storage Temperature Zone: 30 Refrige./DoNot Freez, Item Size Code:1ML, Item Strength Code:40MCG/ML, Item Abbreviation: Recombivax Pf, Generic Form: Vial
These highlights do not include all the information needed to use RECOMBIVAX HB safely and effectively. See full prescribing information for RECOMBIVAX HB.
RECOMBIVAX HB® Hepatitis B Vaccine (Recombinant)
Suspension for intramuscular injection
Initial U.S. Approval: 1986
INDICATIONS AND USAGE
RECOMBIVAX HB is a vaccine indicated for prevention of infection caused by all known subtypes of hepatitis B virus. RECOMBIVAX HB is approved for use in individuals of all ages. RECOMBIVAX HB Dialysis Formulation is approved for use in predialysis and dialysis patients 18 years of age and older. (1)
DOSAGE AND ADMINISTRATION
RECOMBIVAX HB
Persons from birth through 19 years of age: A series of 3 doses (0.5 mL each) given on a 0-, 1-, and 6-month schedule. (2.1)
Adolescents 11 through 15 years of age: A series of either 3 doses (0.5 mL each) given on a 0-, 1-, and 6-month schedule or a series of 2 doses (1.0 mL) on a 0- and 4- to 6-month schedule). (2.1)
Persons 20 years of age and older: A series of 3 doses (1.0 mL each) given on a 0-, 1-, and 6-month schedule. (2.1)
RECOMBIVAX HB Dialysis Formulation
Adults on predialysis or dialysis: A series of 3 doses (1.0 mL each) given on a 0-, 1-, and 6-month schedule. (2.1)
DOSAGE FORMS AND STRENGTHS
RECOMBIVAX HB is a sterile suspension available in the following presentations:
0.5 mL (5 mcg) Pediatric/Adolescent Formulation single-dose vials and prefilled syringes (3, 11, 16.1)
1 mL (10 mcg) Adult Formulation single-dose vials and prefilled syringes (3, 11, 16.1)
RECOMBIVAX HB Dialysis Formulation is a sterile suspension available in the following presentation:
1 mL (40 mcg) single-dose vials (3, 11, 16.1)
CONTRAINDICATIONS
Severe allergic or hypersensitivity reactions (e.g., anaphylaxis) after a previous dose of any hepatitis B-containing vaccine, or to any component of RECOMBIVAX HB, including yeast. (4, 11)
WARNINGS AND PRECAUTIONS
The vial stopper, the syringe plunger stopper, and tip cap contain dry natural latex rubber which may cause allergic reactions in latex-sensitive individuals. (5.1)
Apnea following intramuscular vaccination has been observed in some infants born prematurely. Decisions about when to administer an intramuscular vaccine, including RECOMBIVAX HB, to infants born prematurely should be based on consideration of the individual infant's medical status and the potential benefits and possible risks of vaccination. (5.2)
ADVERSE REACTIONS
In healthy infants and children (up to 10 years of age), the most frequently reported systemic adverse reactions (>1% injections), in decreasing order of frequency, were irritability, fever, diarrhea, fatigue/weakness, diminished appetite, and rhinitis. (6.1)
In healthy adults, injection site reactions and systemic adverse reactions were reported following 17% and 15% of the injections, respectively. (6.1)
To report SUSPECTED ADVERSE REACTIONS, contact Merck Sharp & Dohme LLC at 1-877-888-4231 or VAERS at 1-800-822-7967 or www.vaers.hhs.gov .
DRUG INTERACTIONS
Do not mix RECOMBIVAX HB with any other vaccine in the same syringe or vial. (7.1)
See 17 for PATIENT COUNSELING INFORMATION.
Revised: 4/2023
