Product image of Pandemic Influenza Vaccine H5n1 Astrazeneca (A/Vietnam/1203/2004 (H5n1) Strain (A/Vietnam/1203/2004, Medi 0141000136)) supplied by GNH India

Pandemic Influenza Vaccine H5n1 Astrazeneca

Active Ingredient:
A/Vietnam/1203/2004 (H5n1) Strain (A/Vietnam/1203/2004, Medi 0141000136)
Origin:
EU

Pandemic Influenza Vaccine H5n1 Astrazeneca (A/Vietnam/1203/2004 (H5n1) Strain (A/Vietnam/1203/2004, Medi 0141000136))

A/Vietnam/1203/2004 (H5N1) influenza vaccine, the active ingredient in Pandemic Influenza Vaccine H5n1 Astrazeneca, is a vaccine presented as a lyophilized powder for nasal administration. It is intended to induce immunity against the H5N1 avian influenza virus in adults and at‑risk populations, and can be used in seasonal vaccination campaigns under appropriate public health guidance.

GNH India supplies Pandemic Influenza Vaccine H5n1 Astrazeneca 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 import and distribution.

Manufacturer / TM Owner

Astrazeneca Ab

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Indications & Clinical Uses

Pandemic Influenza Vaccine H5n1 Astrazeneca is used within the influenza vaccine family to prevent infection by the H5N1 avian influenza virus.

  • Pandemic H5N1 influenza: Provides prophylactic immunity against infection with the H5N1 virus in adults.
  • High‑risk occupational exposure: Protects healthcare workers and laboratory personnel who may encounter H5N1.
  • Travel to endemic regions: Reduces risk of acquiring H5N1 for travelers to areas with confirmed avian influenza activity.
  • Outbreak control: Supports public‑health measures during H5N1 outbreaks by immunising at‑risk populations.
  • Vaccination of close contacts: Helps limit spread among family members of infected individuals.

How It Works

  • The vaccine contains inactivated A/Vietnam/1203/2004 (H5N1) virus particles that present hemagglutinin antigens to the nasal mucosa. Upon administration, antigen‑presenting cells capture the viral proteins and stimulate B‑cell and T‑cell responses, leading to the production of neutralising antibodies that block viral attachment and entry, thereby conferring protective immunity. The mucosal route also induces local IgA antibodies, enhancing barrier protection in the respiratory tract.

Side Effects

Administration of the nasal H5N1 vaccine may be associated with a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Nasal congestion: mild blockage or stuffiness in the nose.
  • Sore throat: irritation or discomfort in the throat.
  • Low‑grade fever: temperature rise up to 38 °C.
  • Headache: mild to moderate head pain.
  • Runny nose: watery nasal discharge.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Guillain‑Barré syndrome: rare neurologic disorder causing muscle weakness.
  • Severe respiratory distress: difficulty breathing or wheezing.
  • High fever: temperature above 39 °C persisting more than 24 hours.
  • Neurologic events: seizures or altered consciousness.

Precautions & Warnings

Before prescribing Pandemic Influenza Vaccine H5n1 Astrazeneca, healthcare professionals should consider the following precautions.

  • Pregnancy: safety not established; use only if potential benefits justify the risk.
  • Breastfeeding: limited data; evaluate risk‑benefit before administration.
  • Immunocompromised patients: may exhibit reduced immune response to the vaccine.
  • Known hypersensitivity: avoid in individuals allergic to any vaccine component.
  • Age restrictions: not recommended for children under 18 years of age.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

The nasal H5N1 vaccine can interact with other medicines or vaccines; relevant interactions are listed below.

Major Interactions (Avoid)

  • Live attenuated vaccines: concurrent use may diminish effectiveness of either product.
  • Immunosuppressive therapy: may markedly reduce vaccine‑induced immunity.
  • Antiviral agents (e.g., oseltamivir): can interfere with the development of protective antibodies.

Moderate Interactions (Monitor Closely)

  • Antipyretic medications: may mask post‑vaccination fever, obscuring assessment.
  • Other inactivated influenza vaccines: schedule at least 14 days apart to avoid immune interference.
  • Allergy medications (antihistamines): generally safe but monitor for altered local reactions.

Frequently Asked Questions

Pandemic Influenza Vaccine H5n1 Astrazeneca is a nasal influenza vaccine designed to protect individuals from infection with the H5N1 avian influenza virus. It is employed in public‑health programs to prevent pandemic influenza outbreaks, especially in adults and populations at increased risk of exposure.

The A/Vietnam/1203/2004 strain provides inactivated viral antigens that are recognized by the immune system when delivered to the nasal mucosa. This triggers both systemic and mucosal immune responses, leading to the production of neutralising antibodies and cellular immunity that block the virus from attaching to host cells.

The specific dosing regimen is determined by the prescribing clinician based on regulatory guidelines and patient characteristics. Typically, a single dose administered intranasally is used for primary immunisation, with any booster doses prescribed as needed by the healthcare provider.

Safety data for use in pregnancy and lactation are limited. The vaccine should only be administered when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision should be made in consultation with a qualified healthcare professional.

To place an order, submit an enquiry on the product page at gnhindia.com indicating the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, cold‑chain shipping details and the necessary import documentation.

Compared with alternative H5N1 vaccines, such as those from Sanofi, the Astrazeneca product is administered nasally, which can improve patient acceptance and stimulate mucosal immunity. Efficacy and safety profiles are generally comparable, but specific differences in antigen content, adjuvant use and storage requirements may influence selection.

The vaccine must be stored at 2‑8 °C in a refrigerator, protected from light. It should not be frozen or shaken. Vials should remain in their original packaging until use to maintain stability and potency.

The product is supplied as a lyophilized powder that is reconstituted with the provided diluent. The reconstituted vaccine is then administered as a single intranasal dose, typically using a calibrated nasal spray device, by a trained healthcare professional.

Serious adverse events, although rare, include anaphylactic reactions, Guillain‑Barré syndrome, severe respiratory distress, high fever persisting beyond 24 hours, and neurologic complications such as seizures. Immediate medical attention is required if any of these symptoms occur after vaccination.

The vaccine is contraindicated in individuals with a known hypersensitivity to any component of the formulation, in children under 18 years of age, and in persons with severe immunodeficiency where a reduced immune response is anticipated. Consultation with a physician is essential before administration.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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