GNH USA

Europe — EMA

Influvac Tetra

GNH USA supplies Influvac Tetra (B/Phuket/3073/2013, B/Austria/1359417/202), a influenza vaccine for prevention of influenza B infections.

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?

B/Phuket/3073/2013, B/Austria/1359417/202, the active ingredient in Influvac Tetra, is a vaccine presented as a sterile suspension for intramuscular or subcutaneous use. It is designed to stimulate immunity against the specified influenza B virus strains and is indicated for prevention of influenza B infection in eligible populations.

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 an influenza B vaccine used to prevent infection caused by the included viral strains. - Influenza B (B/Phuket/3073/2013): reduces the risk of seasonal influenza caused by this lineage. - Influenza B (B/Austria/1359417/202): reduces the risk of seasonal influenza caused by this lineage. - Seasonal influenza B overall: contributes to community protection against circulating 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 increase in body temperature. - Headache: mild headache occurring 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 with muscle weakness. - Severe allergic reaction: urticaria, angioedema, or respiratory distress. - Seizures: uncommon neurologic event. - High‑grade fever: persistent fever above 39 °C. - Thrombocytopenia: low platelet count observed in rare cases.

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

Before vaccination, consider the following precautions: - Allergy assessment: avoid if the patient has a known severe allergy to any vaccine component. - Egg allergy: evaluate risk, as the vaccine may contain trace egg protein. - Post‑vaccination observation: monitor the patient for at least 15 minutes for immediate reactions. - Immunocompromised patients: weigh benefits against potential reduced efficacy. - Pregnancy and breastfeeding: discuss with a healthcare professional before administration. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake the vial.

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

Influvac Tetra may interact with other medical products as follows: Major Interactions (Avoid): - Live attenuated vaccines: avoid simultaneous administration to prevent interference. - Immunoglobulin therapy: may diminish vaccine‑induced immunity. - Antiviral agents (e.g., oseltamivir) given within 48 hours: could reduce vaccine effectiveness. Moderate Interactions (Monitor Closely): - Immunosuppressive drugs: monitor antibody response after vaccination. - Systemic corticosteroids: may lower immunogenicity, consider timing of dose.

Frequently asked questions

What is Influvac Tetra used for?+
Influvac Tetra is an influenza B vaccine indicated to prevent seasonal influenza caused by the B/Phuket/3073/2013 and B/Austria/1359417/202 virus strains. It is administered to individuals at risk of flu infection to stimulate protective immunity against these specific influenza B lineages.
How does the active ingredient in Influvac Tetra work?+
The vaccine contains inactivated influenza B virus particles that act as antigens. When injected, they are taken up by antigen‑presenting cells, which trigger B‑cell activation and the production of strain‑specific antibodies. These antibodies neutralise the virus, preventing infection if the person is later exposed.
What is the usual dose of Influvac Tetra?+
The dosing regimen for Influvac Tetra is determined by the prescribing healthcare professional based on age, health status, and local immunisation guidelines. Typically, a single dose is administered intramuscularly or subcutaneously, but the exact volume and schedule are set by the clinician.
Is Influvac Tetra safe during pregnancy or breastfeeding?+
Safety data for Influvac Tetra in pregnancy and lactation are limited. Healthcare providers should evaluate the potential benefits and risks before vaccinating pregnant or breastfeeding individuals. Consultation with a medical professional is recommended to make an informed decision.
How do I order Influvac Tetra from GNH USA?+
To place an order, 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 formulation that specifically includes two influenza B strains, offering broader protection against B lineages compared with some trivalent vaccines that contain only one B strain. Its efficacy and safety profile are comparable to other licensed influenza vaccines, but the exact choice depends on regional strain circulation and clinical guidelines.
What are the storage and handling requirements for Influvac Tetra?+
Influvac Tetra must be stored refrigerated at 2‑8 °C. Keep the vial in its original packaging, protect it from light, and avoid freezing or shaking. Before use, allow the product to reach room temperature if required, and discard any vial that has been exposed to temperatures outside the recommended range.
How is Influvac Tetra administered?+
The vaccine is given by a single intramuscular or subcutaneous injection, usually into the deltoid muscle of the upper arm. Administration should be performed by a qualified healthcare professional following aseptic technique and standard vaccination protocols.
What are the most serious risks associated with Influvac Tetra?+
The most serious adverse events reported include severe allergic reactions such as anaphylaxis and rare neurological conditions like Guillain‑Barré syndrome. Immediate medical attention is required if symptoms of a severe reaction appear after vaccination.
Who should not receive Influvac Tetra?+
Individuals with a documented severe allergy to any component of the vaccine, or those who have experienced a previous severe reaction to an influenza B vaccine, should not receive Influvac Tetra. Contra‑indications should be confirmed by a healthcare professional 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
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 Limited
Origin
EU

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