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 (B/Phuket/3073/2013, Wild Type), Influenza Virus B/Austria/1359417/202, the active ingredient in Influvac Tetra, is a vaccine presented as an injectable suspension for intramuscular or subcutaneous use. It induces active immunity to prevent influenza infection in individuals recommended for seasonal flu vaccination.

GNH India supplies Influvac Tetra 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 Tetra is a quadrivalent influenza vaccine used to prevent seasonal influenza infection.

  • Seasonal influenza: reduces the risk of infection and related complications in the general population.
  • Elderly individuals: helps lower the incidence of severe flu outcomes in people aged 65 and older.
  • Children and adolescents: provides protection against circulating influenza strains in younger age groups.

How It Works

  • Influvac Tetra contains inactivated influenza virus antigens that are recognized by the immune system. Upon intramuscular or subcutaneous injection, the antigens stimulate B‑cell production of strain‑specific antibodies and activate T‑cell responses, establishing active immunity that neutralizes the corresponding influenza viruses upon exposure.

Side Effects

Common side effects are generally mild and transient, reflecting the body's immune response to the vaccine.

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Redness or swelling: localized erythema or edema.
  • Low‑grade fever: temperature elevation up to 38°C.
  • Headache: mild to moderate intensity.
  • Fatigue or malaise: general feeling of tiredness.
  • Muscle aches: transient myalgia.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Guillain‑Barré syndrome: rare neurological disorder with muscle weakness.
  • Seizures: uncommon neurologic event.
  • High fever: temperature above 39°C persisting more than 24 hours.
  • Severe local reaction: extensive swelling or necrosis at injection site.
  • Thrombocytopenia: low platelet count observed in rare cases.

Precautions & Warnings

Before administering Influvac Tetra, consider the following precautions.

  • Allergy screening: avoid use in individuals with known hypersensitivity to any vaccine component.
  • Acute illness: defer vaccination in persons with moderate or severe acute febrile illness.
  • Immunocompromised patients: vaccine may be less effective; assess risk‑benefit.
  • Egg allergy: evaluate severity; vaccine may be used with caution in mild egg‑allergic individuals.
  • Pregnancy and lactation: consult healthcare provider; safety data are limited.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Influvac Tetra may interact with other medical interventions; monitor accordingly.

Major Interactions (Avoid)

  • Severe egg protein allergy: contraindicated due to potential hypersensitivity.
  • History of Guillain‑Barré syndrome following prior influenza vaccination: avoid repeat dosing.

Moderate Interactions (Monitor Closely)

  • Immunosuppressive therapy: may reduce vaccine efficacy; consider timing.
  • Antipyretics (e.g., acetaminophen) taken prophylactically: could blunt antibody response.
  • Live vaccines administered concurrently: generally safe but schedule spacing may be advised.
  • Antiviral medications (e.g., oseltamivir) started shortly before vaccination: may affect immune response.
  • Blood products or immunoglobulins given within 3 months: could interfere with vaccine‑induced immunity.

Frequently Asked Questions

Influvac Tetra is an inactivated influenza vaccine indicated for the prevention of seasonal influenza infection. It is administered to individuals recommended for annual flu vaccination, including adults, children, the elderly, and those at higher risk of complications.

The B/Phuket/3073/2013 component contains inactivated virus particles that stimulate the immune system to produce specific antibodies. These antibodies recognize and neutralize the corresponding influenza B strain, providing protective immunity when the person is exposed to the virus.

The dosage and schedule of Influvac Tetra are determined by the prescribing healthcare professional based on age, health status, and local immunization guidelines. The prescriber will decide the appropriate volume and route for each patient.

Safety data for Influvac Tetra in pregnancy and lactation are limited. Healthcare providers should evaluate the potential benefits and risks before vaccinating pregnant or breastfeeding individuals, and may follow national recommendations for influenza vaccination in these groups.

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 necessary import documentation.

Influvac Tetra is a quadrivalent, inactivated vaccine that includes two influenza A and two influenza B strains, offering broader protection than trivalent formulations. Compared with live‑attenuated vaccines, it is administered via injection and is suitable for a wider range of patients, including those with certain immunocompromising conditions.

Influvac Tetra must be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Prior to administration, allow the product to reach room temperature if required, and use within the expiry date indicated on the vial.

The vaccine is given by a single intramuscular or subcutaneous injection, typically into the deltoid muscle of the upper arm. The exact site and technique are determined by the healthcare professional performing the vaccination.

Serious adverse events are rare but may include anaphylaxis, Guillain‑Barré syndrome, high‑grade fever, seizures, and severe local reactions. Patients should be observed after vaccination and seek immediate medical attention if signs of a severe allergic reaction or neurological symptoms develop.

Individuals with a known severe allergy to any component of the vaccine, those who have experienced Guillain‑Barré syndrome after a previous influenza vaccine, or persons with a contraindication identified by their healthcare provider should not receive Influvac Tetra.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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