GNH USA

Europe — EMA

Influvac

GNH USA supplies Influvac (influenza virus vaccine), a inactivated influenza vaccine for prevention of seasonal influenza caused by influenza A and B

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

Request sourcing

1
Pack/s

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 an inactivated influenza vaccine presented as a solution for injection for intramuscular, subcutaneous use. It prevents influenza infection caused by influenza A and B viruses in individuals at risk.

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 an inactivated influenza vaccine used to prevent infection by influenza A and B viruses.

- Seasonal Influenza: provides active immunity to reduce the risk of contracting flu during the annual season. - Children (≥6 months): protects young patients from influenza‑related illness. - High‑Risk Groups: lowers the chance of severe complications in people with chronic medical conditions.

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 site of administration. - Redness or swelling: localized erythema or edema that resolves within a few days. - Low‑grade fever: transient temperature rise often accompanied by mild headache or 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 occurrence, particularly in children with a history of febrile seizures.

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 after careful assessment of the individual's medical history.

- Allergy assessment: avoid if the patient has a severe allergic reaction to any vaccine component. - Guillain‑Barré history: evaluate risk and consider alternative protection strategies. - Pregnancy: safety data are limited; use only if the potential benefit outweighs the risk. - Immunocompromised patients: vaccine may elicit a reduced immune response; monitor effectiveness. - Storage: 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?

Vaccines may interact with other agents that affect immune function.

Major Interactions (Avoid): - Live vaccines: do not administer concurrently with live attenuated vaccines. - Immunoglobulins or blood products: may diminish vaccine‑induced immunity if given within 3 months. - Antiviral therapy (e.g., oseltamivir) started within 48 h of vaccination: can reduce antibody response.

Moderate Interactions (Monitor Closely): - Immunosuppressive drugs: monitor serologic response as efficacy may be lowered. - Antipyretics taken before vaccination: may blunt the immune response; advise use after injection if needed. - Other injectable vaccines given same day: observe for additive local or systemic reactions.

Frequently asked questions

What is Influvac used for?+
Influvac is an inactivated influenza vaccine indicated for the prevention of influenza infection caused by influenza A and B viruses. It is administered to individuals, including children, adults, and high‑risk groups, to reduce the likelihood of seasonal flu and its complications.
How does the influenza virus vaccine in Influvac work?+
The vaccine contains killed influenza virus antigens that stimulate the immune system to produce antibodies against the hemagglutinin and neuraminidase proteins of the virus. These antibodies recognize and neutralize the virus if the person is later exposed, providing active immunity without causing disease.
What is the usual dose of Influvac?+
The specific dose and schedule of Influvac are determined by the prescribing healthcare professional based on age, health status, and local immunization guidelines. The prescriber will select the appropriate volume and route for each patient.
Is Influvac safe to use during pregnancy or breastfeeding?+
Safety data for Influvac in pregnancy are limited, and the product is classified as having an unknown pregnancy category. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus. Breastfeeding mothers should consult their physician 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 worldwide. After submission, the sales team will verify trade or institutional credentials and provide pricing, availability, shipping details (including cold‑chain handling), and any necessary import documentation.
How does Influvac compare with other influenza vaccines?+
Influvac is an inactivated, trivalent vaccine containing specific strains of influenza A and B, similar to other licensed seasonal flu vaccines. Compared with live‑attenuated or recombinant vaccines, it does not contain live virus and is suitable for a broader range of patients, including those with weakened immune systems, though efficacy may vary by strain match.
What are the storage and handling requirements for Influvac?+
Influvac must be stored in a refrigerator at 2‑8 °C. Keep the vial in its original packaging, protect it from light, and avoid freezing or shaking. Do not use the product if it has been exposed to temperatures outside this range.
How is Influvac administered?+
Influvac is supplied as a sterile solution for injection and is administered by a qualified healthcare professional via the intramuscular or subcutaneous route, typically into the deltoid muscle. The injection technique follows standard aseptic procedures.
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. Patients should be observed for at least 15 minutes after vaccination, 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, or who have experienced a previous severe reaction to an influenza vaccine, should not receive Influvac. Additionally, persons with a recent history of Guillain‑Barré syndrome should discuss risks with their healthcare provider before vaccination.
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 Oy
Origin
EU

Related products