Product image of Influvac Tetra (B/Phuket/3073/2013-Like Virus (B/Phuket/3073/2013, Wild Type), Influenza Virus B/Austria/1359417/202) supplied by GNH India

Influvac Tetra

Active Ingredient:
B/Phuket/3073/2013-Like Virus (B/Phuket/3073/2013, Wild Type), Influenza Virus B/Austria/1359417/202
Origin:
EU

Influvac Tetra (B/Phuket/3073/2013-Like Virus (B/Phuket/3073/2013, Wild Type), Influenza Virus B/Austria/1359417/202)

B/Phuket/3073/2013‑Like Virus (B/Phuket/3073/2013, Wild Type) and Influenza Virus B/Austria/1359417/202, the active ingredients in Influvac Tetra, are a quadrivalent influenza vaccine presented as a vaccine for intramuscular use. It is used to prevent seasonal influenza infection in individuals at risk, including children, adults and the elderly.
GNH India supplies Influvac Tetra as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Viatris Healthcare Limited

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Indications & Clinical Uses

Influvac Tetra is a quadrivalent influenza vaccine indicated for the prevention of influenza caused by the included virus strains.

  • Seasonal influenza: reduces the risk of infection from the four vaccine‑matched influenza viruses.
  • Influenza B infection: provides specific protection against B/Phuket/3073/2013 and B/Austria/1359417/202 strains.
  • High‑risk populations: helps lower the incidence of severe disease in elderly persons, young children, and individuals with chronic health conditions.

How It Works

  • Influvac Tetra contains inactivated influenza virus particles that stimulate the immune system to produce antibodies against the hemagglutinin and neuraminidase antigens of each included strain. The generated antibodies neutralize the virus upon exposure, providing active immunity that reduces infection and disease severity.

Side Effects

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Redness or swelling: localized erythema or edema at the site.
  • Low‑grade fever: transient temperature rise within 24‑48 hours.
  • Headache: mild headache occurring shortly after vaccination.
  • Myalgia: temporary muscle aches.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Guillain‑Barré syndrome: rare neurological disorder that may follow vaccination.
  • Seizures: infrequent occurrence, especially in children with a history of febrile seizures.
  • Severe allergic reaction: angioedema or bronchospasm.
  • Thrombocytopenia: rare drop in platelet count.

Precautions & Warnings

Influvac Tetra should be administered only after evaluating the following considerations.

  • Allergy to vaccine components: avoid if the patient has a known severe allergy to any ingredient.
  • History of severe allergic reaction to previous influenza vaccines: defer administration.
  • Acute febrile illness: postpone vaccination until recovery.
  • Egg allergy: assess risk; vaccine may contain trace egg protein.
  • Immunocompromised status: monitor response, as efficacy may be reduced.
  • Store at 2‑8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Vaccines may interact with other agents that affect immune response.

Major Interactions (Avoid)

  • Live attenuated vaccines: avoid simultaneous administration to prevent interference.
  • Immunoglobulin or blood products given within 3 days: may neutralize vaccine antigens.

Moderate Interactions (Monitor Closely)

  • Antiviral medications (e.g., oseltamivir): may slightly reduce immunogenicity.
  • Immunosuppressive therapy: monitor antibody response, may need revaccination.
  • Corticosteroids at high dose: possible diminished vaccine efficacy.

Frequently Asked Questions

Influvac Tetra is a quadrivalent inactivated influenza vaccine designed to protect against seasonal flu caused by the four virus strains it contains. It is administered to individuals of various ages to reduce the risk of infection, complications, and hospitalization associated with influenza.

The vaccine contains inactivated virus particles that present hemagglutinin and neuraminidase antigens to the immune system. This exposure triggers the production of specific antibodies, which can neutralize the matching influenza viruses if the person is later exposed, thereby providing active immunity.

The dose and schedule of Influvac Tetra are determined by the prescribing healthcare professional based on age, health status, and local immunization guidelines. The vaccine is typically given as a single intramuscular injection each flu season.

Influvac Tetra may be administered to pregnant or breastfeeding individuals when the benefits of influenza protection outweigh potential risks. Healthcare providers assess each case individually, and current guidance generally supports vaccination during pregnancy to protect both mother and infant.

To place an order, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, cold‑chain shipping details and necessary import documentation.

Influvac Tetra is a quadrivalent, inactivated vaccine covering two A strains and two B strains, offering broader protection than trivalent formulations that contain only one B strain. Its safety profile and immunogenicity are comparable to other licensed quadrivalent vaccines, though specific efficacy may vary by population and circulating strains.

The vaccine must be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. It should be kept in its original packaging until use to maintain potency and stability.

Influvac Tetra is given by a single intramuscular injection, usually into the deltoid muscle of the upper arm. The injection is performed by a qualified healthcare professional using aseptic technique.

Serious but rare risks include anaphylaxis, Guillain‑Barré syndrome, and severe allergic reactions such as angioedema or bronchospasm. Immediate medical attention is required if any of these symptoms develop after vaccination.

Individuals with a known severe allergy to any component of the vaccine or who have experienced a severe allergic reaction to a previous dose of an influenza vaccine should not receive Influvac Tetra. Persons with acute febrile illness should postpone vaccination until recovery.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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