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

Influsplit

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

Influsplit (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 Influsplit, is a vaccine presented as an injectable solution for intramuscular use. It induces immunity against influenza A and B viruses and is intended for prophylactic use in individuals at risk of seasonal flu.

GNH India supplies Influsplit as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring quality‑controlled manufacturing, regulatory compliance, and reliable cold‑chain logistics for global distribution, and timely delivery to meet seasonal demand.

Manufacturer / TM Owner

Glaxosmithkline Gmbh & Co. Kg

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Indications & Clinical Uses

Influsplit is a split‑virion influenza vaccine used to prevent infection by influenza A and B viruses.

  • Seasonal influenza (influenza A and B): provides active immunization to reduce the risk of infection and related complications.
  • High‑risk groups (elderly, chronic disease patients): lowers incidence of flu‑associated hospitalization and severe outcomes.
  • Healthcare personnel: decreases transmission potential in clinical environments and protects vulnerable patients.

How It Works

  • Influsplit contains purified split virion antigens from selected influenza A (Victoria lineage) and influenza B (Austria lineage) strains. After intramuscular injection, the viral hemagglutinin and neuraminidase proteins are taken up by antigen‑presenting cells, triggering a humoral immune response that generates strain‑specific neutralizing antibodies and cellular immunity, thereby establishing active protection against subsequent exposure to the matched influenza viruses.

Side Effects

Influsplit may be associated with local and systemic reactions following injection.

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Redness or swelling: localized erythema or edema.
  • Low‑grade fever: transient temperature rise within 24 hours.
  • Headache: mild headache occurring shortly after vaccination.
  • Myalgia: temporary muscle aches.

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: infrequent convulsive episodes, especially in febrile children.

Precautions & Warnings

Before administering Influsplit, consider the following precautions to ensure safe use.

  • Allergy assessment: avoid vaccination in individuals with a history of severe allergic reaction to any component of the vaccine.
  • Acute illness: defer vaccination in persons with moderate or severe febrile illness until recovery.
  • Post‑vaccination observation: monitor recipients for at least 15‑30 minutes for signs of anaphylaxis.
  • Immunocompromised status: consult a specialist before vaccinating patients with severe immunosuppression, as response may be reduced.
  • Store at 2‑8 °C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Influsplit can interact with other medical products; relevant interactions are listed below.

Major Interactions (Avoid)

  • Live viral vaccines: avoid co‑administration within 4 weeks as interference may reduce efficacy.
  • Immunoglobulin or blood products: concurrent use may diminish antibody response to the vaccine.

Moderate Interactions (Monitor Closely)

  • Antiviral agents (e.g., oseltamivir): may slightly affect immune response; schedule vaccination before initiating therapy when possible.
  • Immunosuppressive therapy: may lower vaccine‑induced immunity; monitor antibody titers if clinically indicated.
  • Fever‑reducing medications: antipyretics taken prophylactically can mask mild post‑vaccination symptoms.

Frequently Asked Questions

Influsplit is a split‑virion influenza vaccine indicated for the prophylactic prevention of influenza infection caused by both influenza A and influenza B viruses. It is administered seasonally to reduce the risk of contracting flu and to lessen the severity of disease in individuals who may be exposed.

The vaccine contains purified viral surface antigens from selected influenza A (Victoria) and B (Austria) strains. After intramuscular injection, these antigens are processed by antigen‑presenting cells, prompting the immune system to produce strain‑specific antibodies and cellular immunity that neutralize the virus upon future exposure.

The prescribing healthcare professional determines the appropriate dose. Typically, a single intramuscular injection is given each influenza season, but the exact volume and schedule are set by the clinician based on local guidelines and patient factors.

Safety data for Influsplit in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. It should be used only if the potential benefit justifies any potential risk, and the decision should be made in consultation with a qualified healthcare provider.

To place an order, 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 any necessary import documentation.

Influsplit is a split‑virion formulation containing specific A (Victoria) and B (Austria) strains, similar to many quadrivalent vaccines. Compared with whole‑virus or live‑attenuated options, split‑virion vaccines generally have a favorable safety profile and are suitable for a broad adult population, though efficacy depends on strain match each season.

Influsplit 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. Maintaining the cold chain during transport and storage preserves vaccine potency.

The vaccine is given as a single intramuscular injection, typically into the deltoid muscle of the upper arm. Healthcare professionals should follow aseptic technique, use the appropriate needle size, and observe the patient for a short period after injection for any immediate reactions.

The most serious adverse events reported are severe allergic reactions such as anaphylaxis, and rare neurological conditions like Guillain‑Barré syndrome. Prompt medical attention is required if symptoms of a severe reaction develop after vaccination.

Individuals with a known severe allergy to any component of the vaccine, or those who have experienced a previous anaphylactic reaction to a similar influenza vaccine, should not receive Influsplit. 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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