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 and B/Austria/1359417/202 virus, the active ingredient in Influvac Tetra, is a vaccine presented as an injectable solution for intramuscular or subcutaneous use. It stimulates the immune system to produce protective antibodies against these influenza B strains, helping to prevent influenza infection in eligible individuals such as children and adults.

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.

Manufacturer / TM Owner

Viatris Healthcare Limited

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Indications & Clinical Uses

  • Influvac Tetra is a quadrivalent influenza vaccine used to prevent seasonal influenza caused by specific B virus strains.
  • Seasonal influenza (B/Phuket/3073/2013-like strain): Provides protective immunity to reduce the risk of infection with this circulating B virus.
  • Seasonal influenza (B/Austria/1359417/202 strain): Induces antibody response that lowers the incidence of illness caused by this B virus.
  • Children aged 6 months and older: Helps decrease laboratory‑confirmed influenza cases in pediatric populations.

How It Works

  • The vaccine contains inactivated influenza B virus antigens from the B/Phuket/3073/2013-like and B/Austria/1359417/202 strains. After intramuscular or subcutaneous injection, these antigens are taken up by antigen‑presenting cells, which process and display them to T‑lymphocytes. This activates B‑cells to produce strain‑specific neutralizing antibodies, establishing humoral immunity that can rapidly neutralize the corresponding influenza viruses upon exposure and contributes to immunological memory for future protection.

Side Effects

Common and serious adverse reactions may occur after administration of Influvac Tetra.

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Redness: localized erythema around the injection area.
  • Swelling: temporary edema at the site of administration.
  • Fever: low‑grade temperature rise within 24‑48 hours.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Guillain‑Barré syndrome: rare neurological disorder that may develop after vaccination.

Precautions & Warnings

  • Precautions should be observed before administering Influvac Tetra.
  • Allergy assessment: verify no previous severe reaction to influenza vaccines or any component.
  • Pregnancy and lactation: consult healthcare provider; vaccine may be administered if benefits outweigh potential risks.
  • Immunocompromised patients: vaccine may be less immunogenic; timing should be coordinated with treating physician.
  • Age eligibility: approved for individuals aged 6 months and older.
  • Concurrent medications: no specific contraindication, but inform provider of immunoglobulins or steroids.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Potential drug interactions should be considered when planning vaccination.

Major Interactions (Avoid)

  • Live attenuated vaccines: avoid simultaneous administration; separate by at least 4 weeks.
  • Immunoglobulin therapy: avoid within 2 weeks before or after vaccination.

Moderate Interactions (Monitor Closely)

  • Antipyretic medications (acetaminophen, ibuprofen): prophylactic use may diminish antibody response; monitor.
  • Immunosuppressive drugs (e.g., corticosteroids, chemotherapy): may reduce vaccine efficacy; monitor.
  • Antihistamines: may mask mild allergic reactions; monitor.

Frequently Asked Questions

Influvac Tetra is a quadrivalent influenza vaccine designed to protect against seasonal influenza caused by the B/Phuket/3073/2013-like and B/Austria/1359417/202 virus strains. It is indicated for individuals aged six months and older to reduce the risk of laboratory‑confirmed influenza infection.

The vaccine contains inactivated antigens from two influenza B virus strains. After injection, these antigens are processed by immune cells, prompting B‑lymphocytes to generate strain‑specific neutralizing antibodies. The resulting humoral response provides protective immunity that can quickly neutralize the targeted viruses if the person is exposed.

The dose and schedule are determined by the prescribing healthcare professional based on age, health status, and local immunization guidelines. Typically, a single intramuscular or subcutaneous injection is administered, with any additional doses recommended by national vaccination programs.

Safety data for use in pregnancy and lactation are limited. The vaccine may be administered when the potential benefits to the mother outweigh any theoretical risks to the fetus or infant. Pregnant or nursing individuals should discuss vaccination with their healthcare provider.

To place an order, submit an enquiry on the Influvac Tetra product page at gnhindia.com, specifying 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 targeting two specific influenza B strains, whereas some alternatives may be trivalent or contain different strain combinations. Its formulation is designed for broad protection against circulating B lineages, and it follows EU licensing standards for safety and efficacy.

The vaccine must be stored at 2‑8 °C (refrigerated) in a controlled temperature environment. It should be kept in the original packaging to protect from light, must not be frozen, and should not be shaken. Proper cold‑chain management is essential to maintain potency.

Influvac Tetra is given by a single intramuscular or subcutaneous injection, usually into the deltoid muscle of the upper arm for adults or the anterolateral thigh for infants and young children, following standard aseptic technique.

The most serious adverse events reported are severe allergic reactions such as anaphylaxis and the rare occurrence of Guillain‑Barré syndrome. Recipients should be observed for at least 15 minutes after vaccination, and any signs of a severe reaction require immediate medical attention.

Individuals with a known severe allergy to any component of the vaccine or who have experienced a previous serious reaction to an influenza vaccine should not receive Influvac Tetra. Contraindications also include those who are currently ill with a high fever; vaccination should be deferred until recovery.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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