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 vaccine presented as a quadrivalent influenza preparation for intramuscular administration. It induces an immune response that helps protect individuals against seasonal influenza infection.

GNH India supplies Influvac Tetra as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies, and clinics worldwide, ensuring quality assurance, regulatory compliance, and reliable cold‑chain logistics for vaccine distribution. Our global network facilitates timely delivery to both public and private healthcare providers across Europe, Asia, Africa and the Americas.

Manufacturer / TM Owner

Viatris Healthcare Gmbh

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Indications & Clinical Uses

Influvac Tetra is an influenza vaccine that works within the respiratory viral infection pathway to prevent seasonal flu.

  • Seasonal influenza: provides prophylactic protection against infection caused by the influenza virus strains included in the vaccine.
  • Children (6 months–17 years): reduces the risk of influenza illness and related complications in pediatric populations.
  • Elderly (65 years and older): lowers the likelihood of severe influenza outcomes and hospitalization in older adults.

How It Works

  • Influvac Tetra contains inactivated viral antigens from the specified influenza B strains. After intramuscular injection, the antigens are taken up by antigen‑presenting cells, stimulating a humoral immune response that generates strain‑specific antibodies against hemagglutinin and neuraminidase proteins. The vaccine also activates helper T‑cells, enhancing the overall adaptive immune response and contributing to longer‑lasting protection.

Side Effects

Influvac Tetra may cause local and systemic reactions, most of which are mild and transient.

Common Side Effects

  • Injection site pain: mild soreness at the injection site lasting 1–2 days.
  • Redness or swelling: localized erythema or edema that resolves within a few days.
  • Low‑grade fever: temperature rise up to 38 °C occurring within 24 hours.
  • Headache or muscle aches: transient discomfort reported after vaccination.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Guillain‑Barré syndrome: rare neurological disorder that may develop weeks after vaccination.
  • Seizures: uncommon febrile convulsions, particularly in young children.

Precautions & Warnings

When using Influvac Tetra, certain precautions should be observed to ensure safety and optimal effectiveness.

  • Pregnancy: consult a healthcare professional before vaccination, as safety data are limited.
  • Egg allergy: avoid if the patient has a severe allergy to egg proteins or vaccine constituents.
  • Age restriction: not indicated for children younger than 6 months of age.
  • Immunocompromised individuals: vaccine may elicit a reduced immune response; monitor closely.
  • Fever monitoring: observe for high fever or systemic reactions following administration.
  • Store at 2‑8 °C: keep refrigerated, protect from light, do not freeze or shake the vial.

Avoid Interactions

Influvac Tetra may interact with certain medical products; awareness of these interactions helps maintain vaccine efficacy.

Major Interactions (Avoid)

  • Live attenuated influenza vaccine: avoid co‑administration within 4 weeks to prevent interference.
  • Immunoglobulin or blood products: avoid within 3 months as they may neutralize vaccine antigens.
  • Antiviral medications: concurrent use may diminish antibody response.

Moderate Interactions (Monitor Closely)

  • Antipyretic agents (e.g., acetaminophen) taken prophylactically: may slightly reduce immunogenicity.
  • Immunosuppressive therapy: may lower vaccine effectiveness, requiring assessment.
  • Seasonal antiviral prophylaxis: monitor for potential reduced vaccine benefit.

Frequently Asked Questions

Influvac Tetra is a quadrivalent influenza vaccine designed to protect against seasonal flu caused by the influenza virus strains included in its formulation. It is administered to individuals to reduce the risk of infection, illness, and complications associated with influenza during the yearly flu season.

The vaccine contains inactivated viral antigens from specific influenza B strains. After intramuscular injection, these antigens are recognized by the immune system, prompting antigen‑presenting cells to activate B‑cells and T‑cells. This leads to the production of strain‑specific antibodies that can neutralise the virus if the person is later exposed.

The dosage of Influvac Tetra is determined by a qualified healthcare professional. In most regions, a single intramuscular dose is administered annually to each eligible individual. The prescriber will consider age, health status, and local immunisation guidelines when deciding the exact regimen.

Safety data for Influvac Tetra in pregnancy are limited, so the vaccine should only be given if the potential benefits outweigh any theoretical risks. Breastfeeding is not a contraindication, but mothers should discuss vaccination with their obstetrician or pediatrician to make an informed decision.

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

Influvac Tetra is a quadrivalent vaccine that includes two influenza B strains (B/Phuket/3073/2013‑Like and B/Austria/1359417/202) in addition to two influenza A strains, offering broader protection than trivalent formulations. Its safety profile and immunogenicity are comparable to other licensed quadrivalent vaccines, though specific strain composition may differ.

The vaccine must be stored refrigerated at 2 °C to 8 °C. It should be kept in the original packaging, protected from light, and must never be frozen or shaken. Prior to administration, allow the vial to reach room temperature if required, following the manufacturer’s instructions.

Influvac Tetra is given by a single intramuscular injection, typically into the deltoid muscle of the upper arm for adults or the anterolateral thigh for infants and young children. The injection is performed by a qualified healthcare professional using aseptic technique.

The most serious adverse events are rare and include severe allergic reactions such as anaphylaxis, Guillain‑Barré syndrome, and high‑grade fever that may require medical evaluation. Prompt medical attention is essential if any signs of a severe reaction appear after vaccination.

Influvac Tetra should not be given to children younger than 6 months of age. Individuals with a known severe allergy to any component of the vaccine, especially egg proteins, or those who have experienced a previous severe reaction to an influenza vaccine should avoid it. Consultation with a healthcare provider is advised for any other concerns.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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