AVAXIM®

05/22/2024
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Product Information

  • Name: AVAXIM®
  • Type: Hepatitis A Vaccine Inactivated
  • Form: Suspension for injection (160U/0.5mL)
  • Manufacturer: Sanofi Pasteur SA, Lyon, France
  • Distributor: Sanofi Pasteur Limited, Toronto, Ontario, Canada

Indications and Clinical Use

  • Indication: Active immunization against hepatitis A infection in persons 12 years of age and older.
  • Use Cases:
    • Pre-exposure for travelers to hepatitis A endemic areas, individuals with chronic liver disease, people with hemophilia, users of illicit drugs, MSM, and those in close contact with adoptees from endemic areas.
    • Post-exposure immunization for household and close contacts of hepatitis A cases.
    • Outbreak control in community and institutional settings.

Contraindications

  • Hypersensitivity to any component of AVAXIM® or severe allergic reaction after previous administration of the vaccine or similar vaccines.

Warnings and Precautions

  • General: Inform recipients about the benefits and risks of immunization and assess their health status and immunization history.
  • Protection: Does not protect against hepatitis B, C, delta virus, E, or other liver pathogens.
  • Hematologic: Caution in individuals with bleeding disorders; intramuscular injections may cause hematoma.
  • Immune: Reduced efficacy in immunocompromised individuals.
  • Pregnant and Nursing Women: Limited data; use only if clearly needed.

Adverse Reactions

  • Clinical Trials: Mild and transient, mainly within the first few days post-vaccination. Common reactions include:
    • Local: Pain (11.7%), redness (0.5%).
    • Systemic: Weakness (13.5%), myalgia/arthralgia (10.3%), headache (9.7%), gastrointestinal symptoms (6.1%), mild fever (5.2%).
    • Rare: Mild transient elevation of serum transaminases, injection site nodule.
  • Post-Market: Includes vasovagal syncope, urticaria, rashes, and increased transaminases.

Drug Interactions

  • Vaccine-Drug: Immunosuppressive treatments may interfere with immune response.
  • Concomitant Vaccine Administration: Safe with immune globulin and other vaccines using separate injection sites.

Dosage and Administration

  • Recommended Dose: Single dose of 0.5 mL intramuscularly, with a booster 6-36 months later for long-term protection.
  • Administration: Preferred site is the deltoid muscle. Inspect for particulate matter and discoloration before use. Shake well before administration.

Overdose

  • Management: Contact regional Poison Control Centre.

Action and Clinical Pharmacology

  • Mechanism of Action: Induces production of specific anti-HAV antibodies.
  • Pharmacodynamics: Over 90% protected 14 days post-vaccination, 100% protected one month post-vaccination. Immunity persists for at least 36 months after initial dose.

Storage and Stability

  • Storage: Store at 2° to 8°C, do not freeze. Discard if exposed to freezing. Do not use after the expiration date.

Dosage Forms, Composition, and Packaging

  • Dosage Forms: Pre-filled syringes containing 0.5 mL of sterile, whitish, cloudy suspension.
  • Composition: Includes inactivated hepatitis A virus (GBM strain), aluminum hydroxide, formaldehyde, neomycin, 2-phenoxyethanol, and polysorbate 80.
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Written By Paul Kim

Medical Director - APN, NSWOC, RNP

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