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), Influenza A/Vic, the active ingredient in Influvac, is a vaccine presented as an injectable solution for intramuscular or subcutaneous use. It induces immunity to prevent influenza caused by influenza A and B viruses in at‑risk populations.

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 seasonal influenza vaccine used to prevent infection by influenza A and B viruses.

  • Seasonal influenza prevention: provides active immunity against circulating influenza A (including A/Vic) and B (including B/Austria/1359417/2021‑like) strains.
  • High‑risk population protection: reduces the incidence of flu in elderly, immunocompromised, or individuals with chronic medical conditions.
  • Public health immunisation: contributes to community‑level protection during annual influenza seasons.

How It Works

  • Influvac contains inactivated influenza virus antigens that are recognized by the host immune system. Upon intramuscular or subcutaneous injection, antigen‑presenting cells process the viral proteins and stimulate B‑cell and T‑cell responses, leading to the production of strain‑specific antibodies that neutralise influenza A and B viruses upon subsequent exposure.

Side Effects

Common Side Effects

  • Injection site pain: mild to moderate soreness at the injection site.
  • Redness or swelling: localized erythema or edema.
  • Low‑grade fever: transient temperature rise within 24‑48 hours.
  • Headache or myalgia: mild headache or muscle aches.
  • Fatigue: temporary feeling of tiredness.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Guillain‑Barré syndrome: rare neurological disorder with muscle weakness.
  • Seizures: infrequent occurrence, especially in individuals with a history of seizures.
  • Severe allergic reaction: hives, swelling of face or throat, difficulty breathing.

Precautions & Warnings

Before receiving Influvac, consider the following precautions.

  • Allergy assessment: avoid if there is a known severe allergy to any vaccine component.
  • Guillain‑Barré history: consult a healthcare professional if the individual has previously experienced Guillain‑Barré syndrome.
  • Pregnancy considerations: discuss vaccination with a physician to weigh benefits and risks.
  • Immunocompromised status: vaccine may be less effective; monitor immune response.
  • Age limitation: not recommended for children younger than six months.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Influvac may interact with other medical products; monitor as indicated.

Major Interactions (Avoid)

  • Concurrent administration of blood products or immunoglobulins: may diminish vaccine efficacy.
  • Live attenuated vaccines given within 4 weeks: could interfere with immune response.

Moderate Interactions (Monitor Closely)

  • Immunosuppressive therapy (e.g., corticosteroids, chemotherapy): may reduce antibody production.
  • Antipyretic or analgesic use before vaccination: can mask early signs of adverse reactions.
  • Antiviral medications (e.g., oseltamivir) started shortly after vaccination: may affect immune response.
  • Seasonal influenza prophylaxis agents: coordinate timing to avoid overlapping immune stimulation.

Frequently Asked Questions

Influvac is an inactivated influenza vaccine indicated for the prevention of seasonal influenza caused by influenza A and B viruses. It is administered to individuals at risk of flu infection, including the elderly, people with chronic health conditions, and healthcare workers.

The vaccine contains antigens from the influenza B/Austria/1359417/2021‑like strain and the influenza A/Vic strain. After injection, these antigens stimulate the immune system to produce specific antibodies that neutralise the corresponding viruses, providing protective immunity against future exposure.

The dose of Influvac is determined by the prescribing healthcare professional based on the patient’s age, health status, and local immunisation guidelines. The product is supplied as a single‑dose injectable solution for intramuscular or subcutaneous administration.

Safety data for Influvac in pregnancy and lactation are limited. Healthcare providers should evaluate the potential benefits and risks before vaccinating pregnant or breastfeeding individuals, and vaccination decisions should follow local clinical recommendations.

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 contains the specific B/Austria/1359417/2021‑like and A/Vic strains, matching the current EU seasonal formulation. Compared with other quadrivalent or trivalent vaccines, its antigen composition reflects the WHO‑recommended strains for the 2021‑2022 season, offering comparable efficacy when administered correctly.

Influvac must be stored refrigerated at 2‑8 °C. It should be kept in the original packaging, protected from light, and must not be frozen or shaken. Maintaining the cold chain during transport and storage is essential to preserve vaccine potency.

Influvac is supplied as a sterile injectable solution and is given by a qualified healthcare professional via intramuscular or subcutaneous injection, typically in the deltoid muscle. The injection site should be cleaned with an antiseptic before administration.

The most serious risks include severe allergic reactions such as anaphylaxis, and rare neurological events like Guillain‑Barré syndrome. Recipients should be observed for at least 15 minutes after vaccination, and any signs of severe reaction should be treated immediately.

Individuals with a known severe allergy to any component of the vaccine, those who have experienced a previous severe reaction to an influenza vaccine, or persons with a history of Guillain‑Barré syndrome within six weeks of a prior influenza vaccination should avoid receiving Influvac. Consultation with a healthcare provider is essential for other contraindications.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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