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Havrix Junior

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

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

Havrix Junior is an injectable hepatitis A vaccine that contains inactivated hepatitis A virus adsorbed on aluminium hydroxide. It is supplied as a sterile solution for intramuscular administration and is prescribed in the European Union. The vaccine is designed to stimulate active immunity against hepatitis A infection, primarily in pediatric patients, by prompting the body to produce protective antibodies and to contribute to community health protection.

Manufacturer / TM Owner

Glaxosmithkline Biologicals S.A.

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Indications & Clinical Uses

Havrix Junior is indicated for the prevention of hepatitis A infection in children and is part of routine immunization schedules in many countries.

  • Primary prophylaxis against hepatitis A virus in children aged 12 months and older.
  • Completion of a two‑dose series, typically administered six months apart.
  • Use in outbreak settings to quickly establish herd immunity among pediatric populations.
  • Administration before travel to regions where hepatitis A is endemic.
  • Inclusion in combined vaccination programs when a hepatitis A vaccine is required.

Side Effects

Like other vaccines, Havrix Junior may cause mild to moderate reactions, most of which resolve without medical intervention.

Common

  • Pain, redness, or swelling at the injection site.
  • Low‑grade fever (temperature <38.5 °C).
  • Headache or mild fatigue.
  • Transient loss of appetite.

Serious

  • Allergic reactions such as urticaria, angioedema, or anaphylaxis.
  • Neurological events including Guillain‑Barré syndrome.
  • Persistent high fever or severe systemic illness.

Precautions & Warnings

Healthcare providers should assess individual risk factors and medical history before administering Havrix Junior to ensure safe vaccination.

  • Defer vaccination in children with a known severe allergy to any vaccine component, including aluminium hydroxide.
  • Postpone if the child has an acute moderate or severe illness with fever.
  • Use caution in individuals with a history of Guillain‑Barré syndrome.
  • Evaluate immunocompromised patients on a case‑by‑case basis, as response may be reduced.
  • Discuss pregnancy and breastfeeding status; data are limited, and vaccination decisions should follow local guidelines.
  • Monitor for signs of anaphylaxis for at least 15 minutes after injection.

Avoid Interactions

Havrix Junior generally has a low potential for drug interactions, but certain concomitant therapies may influence its safety or effectiveness.

Avoid

  • Simultaneous administration of other injectable vaccines containing live attenuated viruses, which may interfere with immune response.
  • Use of systemic corticosteroids at immunosuppressive doses immediately before or after vaccination.

Use with caution

  • Antipyretics (e.g., acetaminophen or ibuprofen) may mask low‑grade fever; they can be given after vaccination if needed.
  • Immunoglobulin or blood products given within four weeks before or after vaccination may reduce antibody response.
  • Antihistamines may be used to manage mild allergic reactions but do not prevent serious hypersensitivity.

Frequently Asked Questions

Havrix Junior is approved for use in children aged 12 months and older for hepatitis A prevention.

A complete series consists of two intramuscular injections given at least six months apart.

It may be administered with inactivated vaccines, but simultaneous use with live attenuated vaccines is generally avoided.

Common reactions include pain, redness, or swelling at the injection site, low‑grade fever, headache, fatigue, and temporary loss of appetite.

Vaccination should be deferred in children with a known severe allergy to any component of the vaccine, such as aluminium hydroxide.

Vaccination is postponed if the child has an acute moderate or severe illness with fever; mild illness without fever may not require delay.

Data are limited; vaccination decisions for pregnant or nursing mothers should follow local health authority recommendations.

Rare serious events include severe allergic reactions (anaphylaxis), Guillain‑Barré syndrome, and persistent high fever or severe systemic illness.

Antipyretics can be used after vaccination to manage fever or discomfort but may mask low‑grade fever; they do not significantly affect immunogenicity.

Clinical studies show that protective antibodies persist for many years, often providing long‑term immunity, though exact duration varies among individuals.

Immunoglobulin or blood products given within four weeks before or after vaccination may reduce the antibody response to Havrix Junior.

Seek immediate medical attention; anaphylaxis requires emergency treatment, and the event should be reported to health authorities.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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