GNH USA

Europe — EMA

Influvac Tetra

GNH USA supplies Influvac Tetra (influenza virus vaccine), a quadrivalent vaccine for prevention of influenza caused by B/Phuket/3073/2013

B/Phuket/3073/2013-Like Virus (B/Phuket/3073/2013, Wild Type), Influenza Virus B/Austria/1359417/202

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What is B/Phuket/3073/2013-Like Virus (B/Phuket/3073/2013, Wild Type), Influenza Virus B/Austria/1359417/202?

influenza virus vaccine (quadrivalent), the active ingredient in Influvac Tetra, is a vaccine presented as an injectable solution for intramuscular or subcutaneous use. It prevents influenza infection caused by specific B virus strains in eligible individuals.

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

What is B/Phuket/3073/2013-Like Virus (B/Phuket/3073/2013, Wild Type), Influenza Virus B/Austria/1359417/202 used for?

Influvac Tetra is a quadrivalent influenza vaccine indicated for the prevention of influenza caused by specific virus strains.

- Influenza B/Phuket/3073/2013-like strain: prevention of influenza infection caused by this strain - Influenza B/Austria/1359417/202-like strain: prevention of influenza infection caused by this strain - Seasonal influenza (quadrivalent formulation): broader protection against circulating influenza B viruses

What are the side effects of B/Phuket/3073/2013-Like Virus (B/Phuket/3073/2013, Wild Type), Influenza Virus B/Austria/1359417/202?

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: mild headache within 24 hours - Myalgia: muscle aches or soreness - Fatigue: temporary feeling of tiredness

Serious or Rare Side Effects: - Anaphylaxis: severe allergic reaction requiring immediate medical attention - Guillain‑Barré syndrome: rare neurological disorder post‑vaccination - Seizures: uncommon neurologic event - High fever: temperature > 39 °C persisting beyond 48 hours - Severe allergic reaction: hives, swelling of face or throat - Vasovagal syncope: fainting episode after injection

What precautions apply to B/Phuket/3073/2013-Like Virus (B/Phuket/3073/2013, Wild Type), Influenza Virus B/Austria/1359417/202?

Precautions should be observed before administering Influvac Tetra.

- Allergy assessment: avoid in persons with severe allergy to any vaccine component - History of Guillain‑Barré syndrome: evaluate risk and discuss with healthcare provider - Pregnancy: consult a healthcare professional; vaccine may be used if benefits outweigh risks - Immunocompromised patients: may have reduced immune response; monitor effectiveness - Age restrictions: approved for individuals aged 6 months and older - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake

What does B/Phuket/3073/2013-Like Virus (B/Phuket/3073/2013, Wild Type), Influenza Virus B/Austria/1359417/202 interact with?

Potential interactions with other medicines or vaccines should be considered.

Major Interactions (Avoid): - Live attenuated influenza vaccine: do not co‑administer with this inactivated vaccine - Immunoglobulin therapy: may diminish vaccine efficacy if given concurrently

Moderate Interactions (Monitor Closely): - Antipyretics (e.g., acetaminophen, ibuprofen): may be used for fever but could slightly blunt antibody response - Immunosuppressive drugs: monitor immune response and consider timing of vaccination - Other vaccines: can be given at separate anatomical sites on the same day

Frequently asked questions

What is Influvac Tetra used for?+
Influvac Tetra is a quadrivalent influenza vaccine used to prevent influenza infection caused by the B/Phuket/3073/2013‑like and B/Austria/1359417/202‑like virus strains. It is administered to individuals who need protection against seasonal influenza as part of routine immunisation programmes.
How does the influenza virus vaccine (quadrivalent) work?+
The vaccine contains inactivated antigens from four influenza virus strains. When injected, these antigens stimulate the immune system to produce specific antibodies against the haemagglutinin and neuraminidase proteins of the included strains, providing active immunity that can neutralise the virus upon future exposure.
What is the usual dose of Influvac Tetra?+
The dose of Influvac Tetra is determined by the prescribing healthcare professional based on age, health status and local immunisation guidelines. The vaccine is typically given as a single intramuscular or subcutaneous injection, with repeat dosing as recommended by national health authorities.
Is Influvac Tetra safe during pregnancy or breastfeeding?+
Safety data for Influvac Tetra in pregnancy are limited, so the vaccine should only be used if the potential benefits outweigh any potential risks. Breastfeeding is not a contraindication, but women should discuss vaccination with their healthcare provider to make an informed decision.
How do I order Influvac Tetra from GNH USA?+
To order Influvac Tetra, 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 Tetra compare with other influenza vaccines?+
Influvac Tetra is a quadrivalent, inactivated vaccine that targets two B‑virus lineages, offering broader coverage than trivalent formulations that include only one B strain. Compared with live‑attenuated vaccines, it is administered via injection 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 for Influvac Tetra?+
Influvac Tetra 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. If temperature excursions occur, the product should be inspected for any signs of damage before use.
How is Influvac Tetra administered?+
The vaccine is supplied as an injectable solution and is administered by a qualified healthcare professional via intramuscular or subcutaneous injection, typically into the deltoid muscle of the upper arm or the anterolateral thigh in younger children.
What are the most serious risks associated with Influvac Tetra?+
Serious but rare risks include anaphylactic reactions, Guillain‑Barré syndrome, high‑grade fever, seizures and severe allergic responses. Recipients should be observed for at least 15 minutes after injection, and any signs of a serious reaction require immediate medical attention.
Who should not receive Influvac Tetra?+
Individuals with a known severe allergy to any component of the vaccine, those who have experienced a previous severe reaction to an influenza vaccine, or persons with a history of Guillain‑Barré syndrome within six weeks of a prior influenza vaccination should avoid receiving Influvac Tetra unless advised otherwise by a healthcare professional.
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
B/Phuket/3073/2013-Like Virus (B/Phuket/3073/2013, Wild Type), Influenza Virus B/Austria/1359417/202
Route
Intramuscular Use , Subcutaneous Use
Manufacturer
Viatris Healthcare Nv/Sa
Origin
EU

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