Product image of Influvac (Influenza Virus B/Austria/1359417/2021-Like Strain (B/Austria/1359417/2021, Bvr-26), Influenza A/Vic) supplied by GNH India

Influvac

Active Ingredient:
Influenza Virus B/Austria/1359417/2021-Like Strain (B/Austria/1359417/2021, Bvr-26), Influenza A/Vic
Origin:
EU

Influvac (Influenza Virus B/Austria/1359417/2021-Like Strain (B/Austria/1359417/2021, Bvr-26), Influenza A/Vic)

Influenza Virus B/Austria/1359417/2021‑Like Strain (B/Austria/1359417/2021, Bvr‑26) and Influenza A/Vic, the active ingredient in Influvac, is an inactivated influenza vaccine presented as an injectable solution for intramuscular or subcutaneous use. It stimulates the immune system to produce antibodies that protect against seasonal influenza A and B viruses in adults and children as recommended by health authorities.

GNH India supplies Influvac as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide and meets EU regulatory standards through its global distribution network.

Manufacturer / TM Owner

Viatris Medical

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Indications & Clinical Uses

Influvac is an inactivated influenza vaccine indicated for prevention of influenza infection caused by influenza A and B viruses.

  • Seasonal Influenza (A and B): Reduces incidence of laboratory‑confirmed influenza and associated illness.
  • High‑Risk Populations (elderly, chronic disease): Lowers risk of severe disease and hospitalization.
  • Children (6 months to 17 years): Decreases occurrence of flu and school absenteeism.

How It Works

  • Influvac contains split‑virion antigens from selected influenza A (Victoria lineage) and influenza B (Austria lineage) strains. After intramuscular or subcutaneous injection, the inactivated viral proteins are taken up by antigen‑presenting cells, which process and display hemagglutinin and neuraminidase epitopes to T‑cells. This activates B‑cell differentiation and stimulates production of strain‑specific neutralizing antibodies, establishing active immunity without causing infection.

Side Effects

Influvac, like other inactivated influenza vaccines, may be associated with local and systemic reactions.

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Redness or swelling: transient local inflammation.
  • Low‑grade fever: usually resolves within 24‑48 hours.
  • Headache or muscle aches: mild and self‑limiting.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Guillain‑Barré syndrome: rare neurological disorder reported post‑vaccination.
  • High fever or seizures: uncommon but may occur, especially in young children.

Precautions & Warnings

Precautions should be observed when administering Influvac.

  • Assess allergy history: verify no previous severe reaction to influenza vaccines or egg proteins.
  • Delay vaccination: postpone if the individual has an acute moderate or severe illness.
  • Monitor after injection: observe for at least 15 minutes for immediate hypersensitivity.
  • Avoid in individuals with known hypersensitivity to any vaccine component.
  • Pregnancy and lactation: consult a healthcare provider; data are limited.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Potential drug interactions with Influvac are limited but should be considered.

Major Interactions (Avoid)

  • Live vaccines: avoid co‑administration within 4 weeks due to potential interference.
  • Immunosuppressive therapy: may reduce vaccine efficacy; consider timing of administration.
  • Severe egg allergy: contraindicated if the vaccine contains residual egg protein.
  • Antiviral medications (e.g., oseltamivir) taken within 48 hours may blunt immune response.

Moderate Interactions (Monitor Closely)

  • Other inactivated vaccines: can be given concomitantly at different sites.
  • Immunoglobulin therapy: may interfere with antibody response; schedule appropriately.
  • Febrile illness: monitor for increased fever post‑vaccination.

Frequently Asked Questions

Influvac is an inactivated influenza vaccine indicated to prevent infection caused by seasonal influenza A and B viruses. It is administered to individuals, including adults, children, and high‑risk groups, to reduce the likelihood of flu illness, complications, and related hospitalizations.

The vaccine contains split‑virion antigens from selected influenza A (Victoria) and B (Austria) strains. After injection, antigen‑presenting cells display hemagglutinin and neuraminidase fragments to the immune system, prompting B‑cell activation and production of strain‑specific neutralizing antibodies that confer active immunity without causing disease.

The prescribed dose of Influvac is determined by the treating healthcare professional. Typically, a single 0.5 ml intramuscular or subcutaneous injection is given once per influenza season, but the exact regimen may vary based on age, health status, and local immunization guidelines.

Safety data for Influvac in pregnancy and lactation are limited. Healthcare providers should evaluate the risk‑benefit profile for each individual. Pregnant or breastfeeding persons should discuss vaccination with their clinician, who can consider current recommendations and available evidence.

To order Influvac, submit an enquiry on the 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 is an inactivated split‑virion vaccine, similar to many seasonal flu products. Compared with live‑attenuated nasal sprays, it is administered by injection and does not contain live virus, making it suitable for immunocompromised individuals. Its strain composition aligns with WHO recommendations, offering comparable protection to other licensed inactivated vaccines.

Influvac must be stored refrigerated at 2‑8 °C. Keep the vials in the original packaging, protect them from light, and avoid freezing or shaking. If the cold chain is broken, the vaccine should not be used and must be returned to the supplier for proper disposal.

Influvac is given as a single intramuscular or subcutaneous injection, usually into the deltoid muscle of the upper arm or the anterolateral thigh in younger children. The injection should be performed by a qualified healthcare professional using aseptic technique.

The most serious adverse events reported with Influvac are severe allergic reactions such as anaphylaxis and, rarely, Guillain‑Barré syndrome. Immediate medical attention is required if signs of anaphylaxis (e.g., difficulty breathing, swelling of the face) occur after vaccination.

Influvac should be avoided in individuals with a known severe allergy to any component of the vaccine, including egg protein if present, or who have experienced a previous severe reaction to an influenza vaccine. Persons with acute moderate or severe illness should defer vaccination until recovery.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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