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 (inactivated) that contains inactivated hepatitis A virus and the adjuvant algeldrate. It is supplied as an injectable solution for intramuscular administration and is marketed in the European Union. The vaccine is prescribed to stimulate active immunity against hepatitis A infection and is available only by prescription.

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 at risk. It is used in a variety of clinical situations to provide protective immunity.

  • Routine immunization of adults and children aged 1 year and older.
  • Pre‑travel protection for persons traveling to regions with high hepatitis A prevalence.
  • Outbreak control in communities or institutions where hepatitis A cases have occurred.
  • Post‑exposure prophylaxis for individuals who have been exposed to hepatitis A virus.
  • Protection of people with chronic liver disease or clotting factor disorders.

Side Effects

Side effects of Havrix are generally mild and transient, but serious reactions can occur in rare cases.

Common

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

Serious

  • Severe allergic reaction (anaphylaxis) characterized by difficulty breathing, swelling of the face or throat.
  • Guillain‑Barré syndrome (rare neurological disorder).
  • High fever persisting more than 48 hours.
  • Seizures (rare).

Precautions & Warnings

Before administering Havrix, certain precautions should be considered to ensure safety.

  • Do not vaccinate individuals with a known severe allergy to any vaccine component, including algeldrate.
  • Use caution in pregnant or breastfeeding women; discuss potential benefits and risks with a healthcare professional.
  • Immunocompromised patients may have a reduced immune response; vaccination should be evaluated on a case‑by‑case basis.
  • Defer vaccination in persons with an acute moderate or severe febrile illness until recovery.
  • Children under 1 year of age are not approved for this vaccine.
  • Ensure the recommended dosing interval is maintained for optimal protection.

Avoid Interactions

Havrix has limited known drug interactions, but certain situations require attention.

Avoid

  • Simultaneous administration of other injectable vaccines unless specifically recommended by guidelines.
  • Use in individuals who have received a recent blood product that may contain hepatitis A antibodies.

Use with caution

  • Patients receiving immunosuppressive therapy, as vaccine efficacy may be reduced.
  • Concurrent use of antipyretics or analgesics that could mask fever after vaccination.
  • Individuals on long‑term corticosteroid therapy.
  • Co‑administration with live vaccines; maintain appropriate interval as advised.

Frequently Asked Questions

Havrix is an inactivated hepatitis A vaccine that contains killed hepatitis A virus and an aluminum‑based adjuvant (algeldrate). It stimulates the immune system to produce antibodies that protect against future hepatitis A infection.

Havrix is recommended for adults and children aged 1 year and older who are at risk of hepatitis A, including travelers to endemic areas, people with chronic liver disease, and those exposed to the virus.

The typical schedule consists of two doses given intramuscularly. The second dose is administered 6 to 12 months after the first dose to achieve long‑term protection.

The safety of Havrix during pregnancy has not been fully established. Healthcare providers should weigh the potential benefits against any unknown risks before vaccinating pregnant or breastfeeding women.

Common side effects include pain, redness, or swelling at the injection site, low‑grade fever, headache, fatigue, muscle aches, and occasional nausea. These reactions are usually mild and resolve within a few days.

Serious reactions are rare but may include severe allergic responses (anaphylaxis), Guillain‑Barré syndrome, high fever lasting more than 48 hours, or seizures. Immediate medical attention is required if these occur.

Havrix can be given with other vaccines, but simultaneous injection of multiple injectable vaccines should follow local guidelines. Some authorities recommend spacing live vaccines apart from Havrix.

The vaccine should be stored in a refrigerator at 2–8 °C (36–46 °F) and protected from light. Do not freeze. Once removed from refrigeration, use within the time frame specified by the manufacturer.

Yes, Havrix can be used for post‑exposure prophylaxis to prevent hepatitis A infection after a known exposure, typically as a single dose administered as soon as possible.

If a scheduled dose is missed, it should be administered as soon as possible. The subsequent dose should follow the recommended interval to complete the series.

People with immunosuppression may receive Havrix, but the immune response may be reduced. Vaccination decisions should be individualized and discussed with a healthcare professional.

Havrix is an inactivated vaccine using algeldrate as an adjuvant, whereas other hepatitis A vaccines may use different adjuvants or formulations. All provide protection, but dosing schedules and specific indications can vary.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

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