HAVRIX®

05/22/2024
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Product Information

  • Name: HAVRIX®
  • Type: Hepatitis A Vaccine, Inactivated
  • Form: Suspension for injection
  • Manufacturer: GlaxoSmithKline Inc.
  • Distributor: GlaxoSmithKline Inc., Mississauga, Ontario, Canada

Indications and Clinical Use

  • Indication: Active immunization against hepatitis A virus (HAV) infection.
  • Use: Approved for individuals 12 months of age and older. Primary immunization should be administered at least 2 weeks prior to anticipated exposure to HAV.

Contraindications

  • Known hypersensitivity to any component of the vaccine or its container.
  • Severe febrile illness is a contraindication for vaccination, though minor infections are not.

Warnings and Precautions

  • General: Appropriate medication should be available in case of anaphylactic reactions. Supervise vaccinees for 30 minutes post-immunization.
  • Immune System: Reduced efficacy in immunocompromised individuals; may require additional doses.
  • Pregnant and Nursing Women: Use only if clearly needed; risks to the fetus are considered negligible.
  • Hematologic: Caution in individuals with thrombocytopenia or bleeding disorders due to risk of bleeding at injection site.

Adverse Reactions

  • Very Common (≥10%): Irritability, headache, pain, and redness at the injection site, fatigue.
  • Common (≥1% and <10%): Loss of appetite, drowsiness, gastrointestinal symptoms, injection site swelling, fever.
  • Uncommon (≥0.1% and <1%): Upper respiratory tract infection, dizziness, rash, musculoskeletal stiffness.
  • Rare (≥0.01% and <0.1%): Hypoaesthesia, paraesthesia, pruritus, chills.
  • Post-Market Reactions: Anaphylaxis, allergic reactions, convulsions, vasculitis, angioneurotic oedema, urticaria, erythema multiforme, arthralgia.

Drug Interactions

  • Can be administered with other inactivated vaccines and immune globulin (human) but should be given at separate sites.
  • No significant interactions with concomitantly administered recombinant hepatitis B vaccine (ENGERIX-B), typhoid, yellow fever, cholera, tetanus, MMR, or varicella vaccines.

Dosage and Administration

  • Primary Immunization:
  • Adults (19+ years): Single dose of HAVRIX 1440 (1 mL suspension).
  • Children and Adolescents (1-18 years): Single dose of HAVRIX 720 Junior (0.5 mL suspension).
  • Booster Dose: Recommended 6-12 months after the primary dose to ensure long-term protection.
  • Administration: Intramuscular injection in the deltoid region for adults and children, antero-lateral thigh for young children. Not for intravenous use.

Overdose Management

  • Contact regional Poison Control Centre. Adverse events reported following overdose are similar to those with normal administration.

Action and Clinical Pharmacology

  • Mechanism of Action: Induces production of specific anti-HAV antibodies.
  • Immune Response: High seroconversion rates observed in clinical studies, with over 99% of subjects developing antibodies within one month post-vaccination.

Storage and Stability

  • Store at 2-8°C, do not freeze. Discard if frozen. Stable at temperatures up to 25°C for 3 days.

Dosage Forms, Composition, and Packaging

  • HAVRIX 1440: 1440 ELISA Units/mL for adults.
  • HAVRIX 720 Junior: 720 ELISA Units/0.5 mL for children.
  • Components: Formaldehyde-inactivated hepatitis A virus adsorbed onto aluminium hydroxide. Contains amino acids, disodium phosphate, monopotassium phosphate, polysorbate 20, potassium chloride, sodium chloride, water for injection, and trace neomycin sulphate.
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Written By Paul Kim

Medical Director - APN, NSWOC, RNP

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