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Havrix

Active Ingredient:
Hepatitis A Virus (Inactivated ) Adsorbed On Aluminium Hydroxide Hydrated Produced On Human Diploid
Origin:
EU

Havrix (Hepatitis A Virus (Inactivated ) Adsorbed On Aluminium Hydroxide Hydrated Produced On Human Diploid)

Havrix is an injectable solution containing the inactivated hepatitis A virus adsorbed on aluminium hydroxide hydrated, produced on human diploid cells. It is supplied without a specified strength and is administered intramuscularly. Classified as a vaccine (ATC code J07BC01), Havrix is prescribed for hepatitis A prophylaxis in the European market. It stimulates the immune system to produce antibodies that protect against hepatitis A infection, useful for travelers and outbreak control.

Manufacturer / TM Owner

Glaxosmithkline Single Member A.E.B.E.

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Indications & Clinical Uses

Havrix is indicated for active immunization against hepatitis A virus in several clinical situations.

  • Prevention of hepatitis A infection in individuals at increased risk, such as those with chronic liver disease.
  • Pre‑travel protection for persons traveling to regions where hepatitis A is endemic.
  • Immunization of close contacts during hepatitis A outbreak investigations.
  • Post‑exposure prophylaxis for individuals who have been exposed to hepatitis A and are not immune.
  • Routine vaccination of children and adolescents according to national immunization schedules where applicable.

Side Effects

The safety profile of Havrix reflects the typical reactions seen with inactivated vaccines, most of which are mild and self‑limiting.

Common

  • Pain, redness, or swelling at the injection site.
  • Mild fever.
  • Headache.

Serious

  • Severe allergic reaction (anaphylaxis) with breathing difficulty or swelling.
  • Guillain‑Barré syndrome, a rare neurological disorder.
  • High‑grade fever lasting more than 48 hours.

Precautions & Warnings

Before administering Havrix, healthcare providers should consider several precautionary measures to ensure safe use.

  • Do not vaccinate individuals with a known severe allergy to any component of the vaccine.
  • Defer vaccination in persons who have experienced a severe allergic reaction to a previous dose of Havrix.
  • Use with caution in pregnant or breastfeeding women; benefits should outweigh potential risks.
  • Evaluate immunocompromised patients individually, as response may be reduced.
  • Monitor for signs of anaphylaxis for at least 15 minutes after injection.
  • Postpone vaccination in persons with acute moderate or severe illness until recovery.

Avoid Interactions

Havrix has limited known drug interactions, but certain substances may affect its administration or immune response.

Avoid

  • Concurrent administration of other injectable vaccines at the same anatomical site, which may increase local reactions.
  • Simultaneous administration with live attenuated vaccines at the same site.

Use with caution

  • Immunoglobulin or blood products given within 2 weeks before or after vaccination, as they may blunt antibody response.
  • Systemic corticosteroids or other immunosuppressive therapies, which could reduce vaccine efficacy.
  • Antipyretics (e.g., acetaminophen) taken prophylactically before vaccination, as they might diminish antibody production.
  • Live vaccines administered within 4 weeks before or after Havrix should be spaced appropriately to avoid interference.

Frequently Asked Questions

Havrix can be administered to individuals from 12 months of age onward, following local immunization schedules.

The standard series consists of two doses given six to twelve months apart; a booster may be recommended for long‑term protection in some populations.

Immunity typically persists for at least 20 years after the full two‑dose series, though exact duration can vary among individuals.

Havrix may be administered during pregnancy if the potential benefits outweigh any theoretical risks; the decision should be made by a healthcare professional.

Common reactions include mild pain, redness, or swelling at the injection site, low‑grade fever, and headache, usually resolving within a few days.

Store the vaccine in a refrigerator between 2 °C and 8 °C (36 °F–46 °F) and protect it from light; do not freeze.

Havrix can be administered with other vaccines at different anatomical sites; simultaneous injection at the same site is not recommended.

Seek immediate medical attention; anaphylaxis requires prompt treatment with epinephrine and emergency care.

Ideally, the first dose should be given at least two weeks before departure, with the second dose completed at least six months later for long‑term protection.

Yes, Havrix is used for outbreak control to quickly immunize at‑risk populations and reduce transmission.

Immunocompromised persons may receive Havrix, but their immune response might be lower; clinicians should assess each case individually.

There are no specific drugs that must be avoided, but immunoglobulins, blood products, and certain immunosuppressants may affect vaccine efficacy and should be timed appropriately.

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GNH India Pharmaceuticals Limited

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Last updated:

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