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 an injectable vaccine containing inactivated hepatitis A virus and the adjuvant algeldrate, supplied as a lyophilized powder for reconstitution. It is marketed in the European Union and is classified as a hepatitis A prophylaxis vaccine. The product is administered intramuscularly to stimulate active immunity against hepatitis A infection. Formulation is designed for use in adults as part of immunization schedules, and it does not contain live virus.

Manufacturer / TM Owner

Glaxosmithkline Biologicals S.A.

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Indications & Clinical Uses

Havrix is indicated for the prevention of hepatitis A infection in individuals who have not been previously immunized.

  • Primary prophylaxis for travelers to endemic areas.
  • Routine immunization of children according to national schedules.
  • Post‑exposure prophylaxis for close contacts of confirmed cases.
  • Immunization of individuals with chronic liver disease.
  • Use in outbreak control settings as recommended by public health authorities.
  • Administration to persons with occupational risk (e.g., laboratory workers handling hepatitis A virus).

Side Effects

Following intramuscular injection, Havrix may be associated with transient local and systemic reactions.

Common

  • Pain, redness, or swelling at the injection site.
  • Low‑grade fever.
  • Headache.
  • Fatigue or mild malaise.
  • Nausea.
  • Muscle aches.
  • Local itching.

Serious

  • Severe allergic reaction (anaphylaxis).
  • Guillain‑Barré syndrome (rare).
  • High fever with chills.
  • Persistent joint pain.
  • Neurological symptoms such as weakness.
  • Severe rash.

Precautions & Warnings

Healthcare providers should assess individual risk factors and medical history before administering Havrix.

  • Defer vaccination in persons with known severe allergy to any vaccine component.
  • Evaluate immunocompromised patients, as response may be reduced.
  • Consider timing of other vaccines; separate administration by at least 4 weeks when possible.
  • Counsel pregnant or breastfeeding women; data are limited, so use only if benefits outweigh risks.
  • Monitor for immediate hypersensitivity reactions for at least 15 minutes after injection.
  • Document prior hepatitis A vaccination to avoid unnecessary repeat dosing.

Avoid Interactions

Havrix generally has a low potential for drug interactions, but certain circumstances warrant caution.

Avoid

  • Concomitant administration of other injectable vaccines containing live attenuated viruses (e.g., measles, mumps, rubella) in the same syringe.

Use with caution

  • Simultaneous receipt of other inactivated vaccines (e.g., influenza) may increase local reactogenicity.
  • Immunoglobulin or blood products given within 2 weeks before or after vaccination may diminish immune response.
  • Antihistamines may mask early signs of an allergic reaction.
  • Corticosteroid therapy may reduce vaccine efficacy.

Frequently Asked Questions

Havrix contains inactivated hepatitis A virus particles that stimulate the immune system to produce antibodies and a cellular response, providing active immunity against hepatitis A.

Anyone who has not been previously immunized against hepatitis A, including travelers to endemic areas, children according to national schedules, and individuals with chronic liver disease.

Havrix is supplied as a lyophilized powder that is reconstituted and injected intramuscularly, typically into the deltoid muscle.

The standard schedule consists of two doses given at least six months apart; a booster may be recommended for certain high‑risk groups after ten years.

Data on use during pregnancy are limited; vaccination should be considered only if the potential benefit outweighs any potential risk.

Common reactions include pain, redness, or swelling at the injection site, low‑grade fever, headache, fatigue, nausea, muscle aches, and mild itching.

Serious but rare events may include severe allergic reactions (anaphylaxis), Guillain‑Barré syndrome, high fever with chills, persistent joint pain, severe rash, or neurological weakness.

Live attenuated vaccines should not be mixed in the same syringe. Inactivated vaccines can be co‑administered but may increase local reactogenicity, so spacing them by a few weeks is often recommended.

Check for severe allergies to vaccine components, assess immunocompromised status, consider pregnancy or breastfeeding, and ensure prior hepatitis A vaccination status is known.

Yes, receiving immunoglobulin or blood products within two weeks before or after vaccination can reduce the immune response to Havrix.

In most EU countries Havrix is classified as prescription‑only and should be administered by a qualified healthcare professional.

The patient should be monitored for at least 15 minutes post‑injection, and any signs of anaphylaxis should be treated immediately with appropriate emergency measures.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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