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 vaccine, the active ingredient in Influvac, is a vaccine presented as an injectable suspension for intramuscular and subcutaneous use. It is intended to prevent seasonal influenza caused by influenza virus types A and B in individuals six months of age and older, reducing the risk of infection and related complications.
GNH India supplies Influvac 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 is a vaccine that targets the influenza virus family to provide prophylactic protection against seasonal flu.

  • Seasonal influenza (A): Induces protective antibodies that lower the incidence of influenza A infection.
  • Seasonal influenza (B): Generates immunity that reduces the risk of influenza B disease.
  • General seasonal influenza: Decreases overall flu‑related illness severity and complications across all age groups.

How It Works

  • Influvac contains inactivated influenza virus antigens that stimulate the host immune system to produce specific antibodies against hemagglutinin and neuraminidase proteins. These antibodies neutralize the virus and prevent its attachment to respiratory epithelial cells, thereby providing active immunity against subsequent exposure to the matched influenza strains.

Side Effects

Common Side Effects

  • Injection site pain: Mild to moderate discomfort at the injection site.
  • Redness or swelling: Localized erythema or edema around the injection area.
  • Low‑grade fever: Transient temperature rise within 24‑48 hours.
  • Headache: Mild headache occurring shortly after vaccination.
  • Myalgia: Muscle aches that resolve within a few days.

Serious or Rare Side Effects

  • Anaphylaxis: Severe allergic reaction requiring immediate medical attention.
  • Guillain‑Barré syndrome: Rare neurological disorder potentially linked to vaccination.
  • Seizures: Uncommon febrile seizures in susceptible individuals.
  • High fever: Persistent temperature above 39°C lasting more than 48 hours.
  • Severe allergic reaction: Angioedema or bronchospasm requiring emergency care.

Precautions & Warnings

Influvac should be administered with consideration of the following precautions.

  • Allergy screening: Avoid use in persons with known hypersensitivity to any vaccine component.
  • Acute illness: Postpone vaccination in individuals with moderate or severe febrile illness.
  • Pregnancy: Consult a healthcare professional; limited safety data are available.
  • Immunocompromised patients: May exhibit reduced immunogenic response; monitor effectiveness.
  • Age restriction: Not recommended for children younger than six months.
  • Store at 2-8°C: Keep refrigerated, protect from light, do not freeze or shake the vial.

Avoid Interactions

Vaccination with Influvac may be influenced by other medical products.

Major Interactions (Avoid)

  • Live attenuated vaccines: Do not co‑administer within four weeks to prevent interference.
  • Immunoglobulins or blood products: May diminish vaccine‑induced immunity if given concurrently.

Moderate Interactions (Monitor Closely)

  • Antipyretics (e.g., acetaminophen): May mask post‑vaccination fever.
  • Immunosuppressive therapy: Could reduce antibody response; assess timing.
  • Other inactivated vaccines: Generally safe together but monitor for additive local reactions.

Frequently Asked Questions

Influvac is an influenza virus vaccine indicated for the prevention of seasonal influenza caused by influenza virus types A and B. It is administered to individuals six months of age and older to reduce the risk of flu infection and associated complications.

The vaccine contains inactivated influenza virus antigens that stimulate the immune system to produce antibodies against the hemagglutinin and neuraminidase proteins of the virus. These antibodies neutralize the virus, preventing it from infecting respiratory cells and providing protective immunity.

The dose of Influvac is determined by the prescribing healthcare professional based on the patient’s age, health status, and local immunization guidelines. The prescriber will select the appropriate volume and administration schedule for each individual.

Safety data for Influvac in pregnancy are limited. Healthcare providers should evaluate the potential benefits and risks before vaccinating pregnant or breastfeeding individuals. Consultation with a medical professional is recommended to make an informed decision.

To order Influvac, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India supplies 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 contains the influenza B/Austria/1359417/2021‑like strain and an A/Vic component, matching the WHO‑recommended seasonal strains. Compared with other quadrivalent or trivalent vaccines, it offers comparable immunogenicity and safety profiles, though specific strain composition may differ between products.

Influvac must be stored at 2‑8 °C in a refrigerator, protected from light. The vial should not be frozen or shaken. Before use, allow the product to reach room temperature for a short period if required, and inspect for any particulate matter or discoloration.

Influvac is given by intramuscular or subcutaneous injection, typically into the deltoid muscle of the upper arm. The administration is performed by a qualified healthcare professional using aseptic technique and the appropriate needle size.

Serious adverse events, although rare, include anaphylaxis, Guillain‑Barré syndrome, high‑grade fever, and severe allergic reactions such as angioedema or bronchospasm. Immediate medical attention is required if any of these symptoms occur after vaccination.

Individuals with a known severe allergy to any component of the vaccine, including egg protein if present, should not receive Influvac. It is also contraindicated for children under six months of age and for persons who have experienced a severe reaction to a previous dose of the same vaccine.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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