Product image of Havrix (Hepatitis A Virus (Inactivated), Algeldrate) supplied by GNH India

Havrix

Active Ingredient:
Hepatitis A Virus (Inactivated), Algeldrate
Origin:
EU

Havrix (Hepatitis A Virus (Inactivated), Algeldrate)

Havrix is a hepatitis A vaccine that contains inactivated hepatitis A virus and the adjuvant algeldrate. It is supplied in a sterile injectable form for intramuscular administration and is marketed in the European Union as a prescription‑only product.

Manufacturer / TM Owner

Glaxosmithkline Biologicals S.A.

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Indications & Clinical Uses

Havrix is indicated for active immunization against hepatitis A virus infection. It is commonly used in the following situations:

  • Prevention of hepatitis A in individuals at risk, such as those with chronic liver disease.
  • Pre‑travel prophylaxis for people visiting regions where hepatitis A is endemic.
  • Immunization of children and adolescents as part of routine vaccination schedules.
  • Protection of laboratory personnel handling hepatitis A specimens.
  • Outbreak control measures in community or institutional settings.

Side Effects

Side effects of Havrix are generally mild and transient, reflecting the body’s immune response to the vaccine.

Common

  • Injection‑site pain, redness, or swelling.
  • Low‑grade fever within 24‑48 hours after vaccination.
  • Headache or mild fatigue.

Serious

  • Severe allergic reaction (anaphylaxis) characterized by difficulty breathing, swelling of the face, or rash.
  • Guillain‑Barré syndrome, a rare neurological condition.
  • Persistent high fever lasting more than three days.
  • Severe joint or muscle pain interfering with daily activities.

Precautions & Warnings

Before receiving Havrix, certain precautions should be considered to ensure safe administration:

  • Verify that the individual has no known severe allergy to any vaccine component, including algeldrate.
  • Defer vaccination in persons with acute moderate or severe illness until recovery.
  • Discuss pregnancy and breastfeeding status with a healthcare professional, as safety data are limited.
  • Assess immune status; immunocompromised patients may have a reduced antibody response.
  • Inform the provider of any history of Guillain‑Barré syndrome.
  • Ensure proper storage and handling of the vaccine according to manufacturer guidelines.

Avoid Interactions

Havrix does not have many documented drug interactions, but certain substances may affect its efficacy or safety.

Avoid

  • Concurrent administration of live vaccines within four weeks, as it may interfere with immune response.
  • Use of immunosuppressive therapies (e.g., high‑dose corticosteroids) immediately before vaccination, which can diminish antibody production.

Use with caution

  • Antipyretics such as acetaminophen or ibuprofen taken around the time of injection, which might mask fever.
  • Blood products or immunoglobulins given within two weeks before or after vaccination.
  • Chronic alcohol consumption, which may impair immune response.
  • Any experimental therapies; consult a healthcare professional before co‑administration.

Frequently Asked Questions

Havrix contains inactivated hepatitis A virus and the adjuvant algeldrate. The inactivated virus stimulates the immune system to produce antibodies, providing active immunity against hepatitis A infection.

Individuals traveling to areas where hepatitis A is common, people with chronic liver disease, children following routine immunization schedules, and laboratory workers handling hepatitis A specimens are typical candidates.

Safety data for Havrix during pregnancy and lactation are limited. Women who are pregnant or breastfeeding should discuss potential benefits and risks with their healthcare provider before vaccination.

The most frequently reported reactions include mild pain, redness, or swelling at the injection site, low‑grade fever, headache, and temporary fatigue.

Protective antibodies typically develop within two to four weeks after the first dose, with full immunity achieved after the complete vaccination series.

Current guidelines suggest that a booster may be considered for individuals at continued risk, but routine boosters are not universally required. Consult a healthcare professional for personalized advice.

Havrix can be co‑administered with most non‑live vaccines, but it should be separated by at least four weeks from live vaccines to avoid potential interference.

If signs of a severe allergic reaction such as difficulty breathing, swelling, or rash develop, seek immediate medical attention and inform the provider about the reaction.

While routine medications do not usually interfere, it is advisable to avoid immunosuppressive drugs immediately before vaccination and to discuss any ongoing treatments with a healthcare professional.

Havrix should be stored in a refrigerator between 2°C and 8°C (36°F‑46°F) and protected from freezing. Follow the manufacturer’s storage instructions to maintain vaccine potency.

Havrix is administered by intramuscular injection, typically into the deltoid muscle of the upper arm.

Havrix is primarily used for pre‑exposure prophylaxis. Post‑exposure prophylaxis may involve immune globulin or a different vaccination schedule; consult a healthcare professional for guidance.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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