GNH USA

Europe — EMA

Influvac

GNH USA supplies Influvac (Influenza virus vaccine), a vaccine for preventing seasonal influenza caused by influenza A and B viruses.

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

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What is 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 a sterile suspension for intramuscular and subcutaneous use. It is designed to prevent influenza infection caused by influenza A and B viruses in individuals aged six months and older.

GNH USA supplies Influvac as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory documentation to support global distribution. All shipments are managed under controlled temperature conditions to preserve vaccine potency.

What is Influenza Virus B/Austria/1359417/2021-Like Strain (B/Austria/1359417/2021, Bvr-26), Influenza A/Vic used for?

Influvac is indicated for the prevention of influenza caused by circulating influenza A and B viruses.

Seasonal influenza: reduces the risk of laboratory‑confirmed influenza infection in the general population. High‑risk groups (e.g., elderly, chronic disease patients): lowers the likelihood of severe disease and related complications. Healthcare workers: helps prevent transmission of influenza in clinical settings.

What are the side effects of Influenza Virus B/Austria/1359417/2021-Like Strain (B/Austria/1359417/2021, Bvr-26), Influenza A/Vic?

Influvac may be associated with local and systemic reactions following administration.

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. - Headache or muscle aches: mild systemic symptoms.

Serious or Rare Side Effects: - Anaphylaxis: severe allergic reaction requiring immediate medical attention. - Guillain‑Barré syndrome: rare neurological disorder reported after influenza vaccination.

What precautions apply to Influenza Virus B/Austria/1359417/2021-Like Strain (B/Austria/1359417/2021, Bvr-26), Influenza A/Vic?

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

- Contraindication: do not vaccinate individuals with a known severe allergy to any vaccine component. - History of Guillain‑Barré syndrome: assess risk and discuss with a healthcare professional. - Acute febrile illness: postpone vaccination until recovery. - Pregnancy: evaluate benefits versus risks with a qualified provider. - Immunocompromised patients: vaccine may be less immunogenic; monitor response. - Store at 2‑8 °C: keep refrigerated, protect from light, do not freeze or shake.

What does Influenza Virus B/Austria/1359417/2021-Like Strain (B/Austria/1359417/2021, Bvr-26), Influenza A/Vic interact with?

Influvac has limited drug interaction potential, but certain co‑administered agents warrant attention.

Major Interactions (Avoid): - Live attenuated vaccines: avoid simultaneous administration; separate by at least 4 weeks. - Immunoglobulin therapy: may reduce vaccine efficacy if given within 2 weeks before or after vaccination.

Moderate Interactions (Monitor Closely): - Antipyretics (e.g., acetaminophen, ibuprofen): may mask fever, but generally safe. - Antiviral medications (e.g., oseltamivir): no direct interaction, but timing may affect immune response. - Immunosuppressive drugs: may diminish antibody response; monitor serologic protection.

Frequently asked questions

What is Influvac used for?+
Influvac is a seasonal influenza vaccine indicated to protect against infection caused by circulating influenza A and B viruses. It is administered to individuals six months of age and older to reduce the risk of flu illness, related complications, and transmission within the community.
How does the influenza virus vaccine work?+
The vaccine contains inactivated virus antigens from selected influenza A and B strains. After injection, antigen‑presenting cells process these proteins and activate T‑cells, which in turn stimulate B‑cells to produce strain‑specific neutralising antibodies. These antibodies provide immunity that can prevent or lessen disease if the person is later exposed to the matching viruses.
What is the usual dose of Influvac?+
The prescribed dose of Influvac is determined by a qualified healthcare professional. Typically, a single intramuscular or subcutaneous injection is given each influenza season, but the exact volume and administration schedule are set by the prescriber based on age, health status, and local immunisation guidelines.
Is Influvac safe during pregnancy or breastfeeding?+
Safety data for Influvac in pregnancy are limited, and the vaccine should only be used when the potential benefits outweigh any theoretical risks. Women who are breastfeeding may receive the vaccine, but they should discuss any concerns with their obstetrician or primary care provider before vaccination.
How do I order Influvac from GNH USA?+
To order Influvac, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams across international markets. After the request, the sales team will verify trade or institutional credentials and respond with pricing, availability, shipping details (including cold‑chain handling) and any required import documentation.
How does Influvac compare with other influenza vaccines?+
Influvac is a split‑virus, inactivated vaccine that includes the latest circulating A and B strains, similar to many other seasonal flu vaccines. Compared with live‑attenuated nasal sprays, Influvac is administered by injection and is suitable for a broader age range, including individuals with certain medical conditions where live vaccines are contraindicated.
How should Influvac be stored and handled?+
Influvac must be stored refrigerated at 2 °C to 8 °C. It should be kept in its original packaging, protected from light, and must not be frozen or shaken. During transport, a validated cold‑chain system is required to maintain the temperature range and preserve vaccine potency.
How is Influvac given or administered?+
Influvac is administered by a single intramuscular or subcutaneous injection, usually into the deltoid muscle of the upper arm. The injection is performed by a qualified healthcare professional using aseptic technique. The site should be observed for a short period after vaccination for any immediate reactions.
What are the most serious risks to watch for with Influvac?+
The most serious adverse events associated with Influvac are severe allergic reactions (anaphylaxis) and the rare occurrence of Guillain‑Barré syndrome. Recipients should be monitored for at least 15 minutes after injection, and any signs of difficulty breathing, swelling of the face or throat, or neurological symptoms should prompt immediate medical evaluation.
Who should not receive Influvac?+
Influvac should not be given to individuals with a known severe allergy to any component of the vaccine, including egg protein if present, or to those who have experienced a previous anaphylactic reaction to an influenza vaccine. Persons with a current severe febrile illness should defer vaccination until they recover.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Influenza Virus B/Austria/1359417/2021-Like Strain (B/Austria/1359417/2021, Bvr-26), Influenza A/Vic
Route
Intramuscular Use , Subcutaneous Use
Manufacturer
Viatris Healthcare Limited
Origin
EU

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