GNH USA

Europe — EMA

Influvac

GNH USA supplies Influvac (Influenza Virus B/Austria/2021, A/Vic), a vaccine for prevention of seasonal influenza. Request a quote for global supply.

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 B/Austria/1359417/2021-Like Strain (B/Austria/1359417/2021, Bvr-26) and Influenza A/Vic, the active ingredient in Influvac, is a vaccine presented as an injectable solution for intramuscular and subcutaneous use. It induces immunity against seasonal influenza in individuals recommended for vaccination.

GNH USA supplies Influvac as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

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

Influvac is a vaccine that targets the influenza virus family to prevent infection and its complications. - Seasonal influenza: reduces the incidence of flu caused by circulating influenza A and B strains. - High‑risk populations (elderly, chronic disease patients): lowers the risk 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?

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 up to 38°C. - 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 with progressive weakness. - High fever or seizures: uncommon but potentially serious systemic reactions.

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

Influvac should be administered with consideration of the following precautions. - Assess allergy history: avoid in individuals with severe egg allergy or known vaccine component hypersensitivity. - Post‑vaccination observation: monitor the recipient for at least 15 minutes for immediate reactions. - Delay vaccination if acute febrile illness is present: postpone until recovery. - Avoid concurrent administration of live vaccines: separate by at least 4 weeks. - 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 may interact with other agents that affect immune response. Major Interactions (Avoid): - Live attenuated vaccines: may interfere with immune response to either product. - Immunoglobulin therapy: can reduce vaccine efficacy. - Immunosuppressive therapy: may diminish antibody production. Moderate Interactions (Monitor Closely): - Antipyretics (acetaminophen, ibuprofen): may mask fever after vaccination. - Antihistamines: may lessen local reaction but do not affect overall immunity.

Frequently asked questions

What is Influvac used for?+
Influvac is an injectable influenza vaccine indicated for the prevention of seasonal influenza. It contains inactivated strains of influenza B (Austria/2021‑like) and influenza A (Victoria) to stimulate protective immunity in individuals who receive the vaccine.
How does the active ingredient in Influvac work?+
The active ingredients are inactivated virus particles that present the immune system with the specific antigens of influenza B/Austria and influenza A/Vic. This exposure triggers the body to produce strain‑specific antibodies and cellular immunity, preparing the immune system to neutralize the live virus if encountered later.
What is the usual dose of Influvac?+
The dosage and administration schedule for Influvac are determined by the prescribing healthcare professional based on local immunization guidelines, the age of the recipient, and any relevant medical considerations. No fixed regimen is provided here.
Is Influvac safe during pregnancy or breastfeeding?+
The safety of Influvac in pregnancy or while breastfeeding has not been definitively established. Healthcare providers should weigh the potential benefits of influenza protection against any uncertain risks and follow national recommendations for vaccinating pregnant or lactating individuals.
How do I order Influvac from GNH USA?+
To request Influvac, submit an enquiry on the product page at gnh-usa.com specifying the required quantity. GNH USA 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.
How does Influvac compare with other influenza vaccines?+
Influvac is a split‑virus, inactivated influenza vaccine containing the same WHO‑recommended B and A strains as many other seasonal flu vaccines. Compared with live‑attenuated nasal sprays, Influvac is administered by injection and is suitable for a broader range of age groups, including those with contraindications to live vaccines.
What are the storage and handling requirements for Influvac?+
Influvac must be stored refrigerated at 2‑8 °C. It should be kept in its original packaging, protected from light, and must never be frozen or shaken. Prior to administration, allow the vial to reach room temperature if required by the label.
How is Influvac administered?+
Influvac is given by a single intramuscular or subcutaneous injection, typically into the deltoid muscle of the upper arm. The exact route and site are chosen by the healthcare professional based on patient age, muscle mass and clinical guidelines.
What are the most serious risks associated with Influvac?+
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 injection, and any signs of a serious reaction should be treated promptly.
Who should not receive Influvac?+
Individuals with a known severe allergy to any component of the vaccine, including egg proteins when present, or those who have experienced a previous severe reaction to an influenza vaccine, should not receive Influvac. Consultation with a healthcare provider is essential for anyone with contraindications.
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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