GNH USA

Europe — EMA

Influvac

GNH USA supplies Influvac (Influenza Virus), a vaccine for prevention of seasonal influenza infection. Request a quote for global supply, available worldwide.

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 ingredients in Influvac, are a vaccine presented as a vaccine for intramuscular/subcutaneous use. It stimulates immunity to prevent influenza infection in children and adults.

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 support for global distribution.

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 active immunization against influenza viruses, targeting the seasonal flu disease family.

Seasonal influenza (A and B strains): reduces the risk of laboratory‑confirmed influenza infection. High‑risk groups (elderly, chronic respiratory or cardiac disease): lowers incidence of severe flu complications. Community outbreaks: contributes to herd immunity by decreasing overall virus circulation.

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

Common and rare adverse reactions may occur after administration of Influvac.

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 hours. - 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 potentially triggered post‑vaccination. - Seizures: infrequent occurrence, especially in children with pre‑existing conditions.

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.

Allergy assessment: avoid if known hypersensitivity to any vaccine component. Pregnancy: consult a healthcare provider to weigh benefits and risks. Immunocompromised patients: vaccine may be less effective; evaluate individual benefit. Fever or acute illness: postpone vaccination until the condition resolves. Concurrent vaccines: separate administration by at least 4 weeks unless otherwise advised. 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 therapies; monitor as indicated.

Major Interactions (Avoid): - Live attenuated vaccines: avoid co‑administration to prevent interference with immune response. - Immunoglobulin therapy: may diminish vaccine efficacy if given concurrently.

Moderate Interactions (Monitor Closely): - Antipyretic medications: may mask post‑vaccination fever, monitor temperature. - Immunosuppressive drugs: reduced antibody response, assess benefit‑risk. - Blood products or plasma: can interfere with immune activation, consider timing.

Frequently asked questions

What is Influvac used for?+
Influvac is a seasonal influenza vaccine indicated for active immunization against influenza A and B viruses, helping prevent flu infection in eligible populations such as children, adults, and high‑risk groups.
How does the active ingredient work?+
The vaccine contains inactivated or subunit antigens derived from the Influenza Virus B/Austria/1359417/2021‑Like strain and Influenza A/Vic. When injected, these antigens are recognized by the immune system, prompting B‑cell and T‑cell activation and the production of strain‑specific antibodies that neutralize the virus upon exposure.
What is the usual dose?+
The prescribed dose of Influvac is determined by the treating healthcare professional based on age, health status and local immunization guidelines. Typically a single intramuscular injection is administered each influenza season, with a second dose only if recommended for certain age groups or immunocompromised patients.
Is Influvac safe in pregnancy or breastfeeding?+
Influvac may be administered to pregnant or lactating individuals when the potential benefits outweigh any theoretical risks. Current data do not indicate specific safety concerns, but vaccination decisions should be made in consultation with a qualified healthcare provider who can evaluate individual circumstances.
How do I order Influvac from GNH USA?+
To place an order, submit an enquiry on the Influvac 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 any necessary import documentation.
How does Influvac compare with other influenza vaccines?+
Influvac is a trivalent (or quadrivalent) inactivated influenza vaccine containing the B/Austria/1359417/2021‑Like strain and A/Vic, offering broad protection similar to other licensed flu vaccines. Compared with live‑attenuated nasal sprays, Influvac is administered by injection, has a well‑established safety profile, and is suitable for a wider range of age groups, including those with certain contraindications to live vaccines.
What are the storage and handling requirements?+
Influvac must be stored at 2 °C to 8 °C (refrigerated) in its original packaging, protected from light. The vaccine should not be frozen or shaken, and any vial that has been frozen or appears cloudy should be discarded. Maintain the cold chain during transport and handling to preserve potency.
How is Influvac administered?+
Influvac is given by a single intramuscular injection, typically into the deltoid muscle of the upper arm. Subcutaneous administration is also acceptable if intramuscular injection is not feasible. The injection should be performed by a qualified healthcare professional using aseptic technique and appropriate needle size.
What are the most serious risks to watch for?+
Although rare, serious adverse events after Influvac may include anaphylaxis, Guillain‑Barré syndrome, and high‑grade fever or seizures. Recipients should be observed for at least 15 minutes after vaccination, and any signs of severe allergic reaction—such as difficulty breathing, swelling of the face or throat, or rapid pulse—require immediate medical attention.
Who should not receive Influvac?+
Individuals with a known severe allergy to any component of Influvac, including egg protein if present, or those who have experienced a previous anaphylactic reaction to an influenza vaccine, should not receive this product. Additionally, persons with acute moderate or severe illness should defer vaccination until recovery.
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 Aps
Origin
EU

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