GNH USA

Europe — EMA

Influvac

GNH USA supplies Influvac (Influenza Virus), a vaccine for prevention of influenza caused by influenza A and B viruses. 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), Influenza A/Vic, the active ingredient in Influvac, is a vaccine presented as an injectable solution for intramuscular or subcutaneous use. It is intended to prevent influenza caused by influenza A and B viruses in individuals at risk, including adults and children.

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 reliable cold‑chain logistics for vaccine 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 an influenza vaccine used to stimulate immunity against seasonal influenza viruses. - Seasonal influenza: reduces the risk of infection with circulating influenza A and B strains. - Influenza outbreaks: provides protective immunity to help control community spread. - High‑risk populations: lowers the likelihood of severe disease and complications in elderly, pregnant persons, and individuals with chronic conditions.

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

Like all vaccines, Influvac may be associated with adverse reactions, most of which are mild and transient.

Common Side Effects: - Injection site pain, redness or swelling. - Low‑grade fever. - Headache. - Muscle aches (myalgia). - Fatigue. - Nausea.

Serious or Rare Side Effects: - Anaphylactic or severe allergic reaction. - Guillain‑Barré syndrome. - High fever or seizures. - Severe local reaction with extensive swelling. - Thrombocytopenia or bleeding disorders.

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

Prior to administration, healthcare providers should evaluate the following precautions to ensure safe use of Influvac. - Contraindication: known severe allergy to any vaccine component or previous severe reaction to influenza vaccine. - Delay vaccination: postpone if the patient has an acute febrile illness until recovery. - Monitoring: observe the patient for at least 15 minutes after injection for signs of allergic reaction. - Pregnancy: consider vaccination if benefits outweigh potential risks; consult a healthcare professional. - Egg allergy: exercise caution in individuals with severe egg protein hypersensitivity, as trace amounts may be present. - 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 certain medical conditions or therapies that affect immune response.

Major Interactions (Avoid): - Live attenuated vaccines: avoid simultaneous administration; schedule at least 4 weeks apart. - Severe immunosuppression (e.g., high‑dose chemotherapy): vaccine may be ineffective and is generally contraindicated.

Moderate Interactions (Monitor Closely): - Moderate immunosuppressive therapy (e.g., low‑dose steroids): may reduce antibody response, monitor serology if needed. - Antiviral medications (e.g., oseltamivir) taken around vaccination: no major effect, but timing can be coordinated. - Chronic illnesses (e.g., uncontrolled diabetes): monitor for heightened reactogenicity.

Frequently asked questions

What is Influvac used for?+
Influvac is an inactivated influenza vaccine indicated for the prevention of seasonal influenza caused by influenza A and B viruses. It is administered to individuals who need protection against circulating flu strains, including adults, children, and people at higher risk of complications such as the elderly or those with chronic health conditions.
How does the active ingredient in Influvac work?+
The vaccine contains antigens derived from selected influenza A and B virus strains. When injected, these antigens are processed by the immune system, stimulating B‑cells to produce strain‑specific antibodies and activating T‑cells. The resulting immune response creates immunological memory, enabling the body to recognise and neutralise the same virus strains if encountered later.
What is the usual dose of Influvac?+
The prescribed dose of Influvac is determined by the treating healthcare professional. Typically, a single dose of the injectable solution is given intramuscularly or subcutaneously each influenza season. The exact volume and administration schedule are set by the prescriber based on age, health status, and local vaccination guidelines.
Is Influvac safe in pregnancy or while breastfeeding?+
Safety data for Influvac in pregnant or lactating individuals are limited, but influenza vaccination is generally recommended when the benefits of preventing flu outweigh potential risks. Healthcare providers should assess each case individually and discuss the decision with the patient, considering current guidelines and the mother’s health condition.
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 supplies hospitals, pharmacies and procurement teams worldwide, and will request verification of trade or institutional credentials. After confirmation, the sales team provides pricing, availability, shipping details—including cold‑chain handling if needed—and assists with any required import documentation.
How does Influvac compare with other influenza vaccines?+
Influvac is an inactivated, split‑virus vaccine that targets the same influenza A and B 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 immunocompromised patients. Its safety and efficacy profile aligns with EU‑approved standards for seasonal influenza immunisation.
How should Influvac be stored and handled?+
Influvac must be stored refrigerated at 2 °C to 8 °C. The vials should be kept in their original packaging, protected from light, and must not be frozen or shaken. Prior to administration, allow the product to reach room temperature if required, and inspect for any discoloration or particulate matter before use.
How is Influvac administered?+
Influvac is supplied as an injectable solution for intramuscular or subcutaneous injection. A qualified healthcare professional selects the appropriate injection site—typically the deltoid muscle for intramuscular delivery or the upper arm for subcutaneous administration—and follows aseptic technique. The dose is administered as a single injection per vaccination season.
What are the most serious risks associated with Influvac?+
Serious adverse events are rare but may include anaphylaxis, a severe allergic reaction that requires immediate medical attention, and Guillain‑Barré syndrome, a neurological disorder that can develop within weeks after vaccination. High fever, seizures, or severe local reactions are also possible. Patients should be observed after injection and instructed to seek care promptly if serious symptoms arise.
Who should not receive Influvac?+
Influvac should be avoided in individuals with a known severe allergy to any component of the vaccine or who have experienced a previous severe reaction to an influenza vaccine. Persons with a history of severe egg allergy should be evaluated carefully, as trace egg protein may be present. Those with acute febrile illness should postpone 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 Hrvatska D.O.O.
Origin
EU

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