Product image of Imovax Polio (Poliovirus (Inactivated) Type 3 (Saukett Strain), Poliovirus (Inactivated) Type 2 (Mef-1 Strain), Po) supplied by GNH India

Imovax Polio

Active Ingredient:
Poliovirus (Inactivated) Type 3 (Saukett Strain), Poliovirus (Inactivated) Type 2 (Mef-1 Strain), Po
Origin:
EU

Imovax Polio (Poliovirus (Inactivated) Type 3 (Saukett Strain), Poliovirus (Inactivated) Type 2 (Mef-1 Strain), Po)

Poliovirus (Inactivated) Type 3 (Saukett Strain), Poliovirus (Inactivated) Type 2 (Mef-1 Strain) and Poliovirus (Inactivated) Type 1 (Mahoney Strain), the active ingredients in Imovax Polio, are an inactivated viral vaccine presented as an injectable solution for intramuscular or subcutaneous use. It induces protective immunity against poliomyelitis caused by poliovirus types 1, 2, and 3 in infants, children and adults.

GNH India supplies Imovax Polio as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide with a focus on quality assurance and regulatory compliance.

Manufacturer / TM Owner

Sanofi Winthrop Industrie

1
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Indications & Clinical Uses

Imovax Polio is an inactivated poliovirus vaccine used to prevent poliomyelitis, a viral infection of the nervous system.

  • Poliomyelitis: Provides active immunity that reduces the risk of disease caused by poliovirus types 1, 2 and 3.
  • Travel to endemic areas: Protects travelers from acquiring poliovirus infection during international trips.
  • Outbreak control: Used in mass vaccination campaigns to interrupt transmission of poliovirus in affected communities.

How It Works

  • The inactivated poliovirus particles retain their capsid antigens but cannot replicate. After intramuscular or subcutaneous injection, antigen‑presenting cells process these proteins, activating B‑cells and helper T‑cells to generate serotype‑specific neutralising antibodies, thereby establishing active immunity against poliovirus types 1, 2 and 3.

Side Effects

Injection of Imovax Polio may be associated with a range of adverse reactions.

Common Side Effects

  • Injection site pain: Mild to moderate discomfort at the site of administration.
  • Redness or swelling: Localised erythema or edema that resolves within a few days.
  • Fever: Transient low‑grade temperature elevation within 24‑48 hours.
  • Headache or irritability: Generalised mild discomfort, especially in children.

Serious or Rare Side Effects

  • Anaphylaxis: Severe allergic reaction requiring immediate medical intervention.
  • Guillain‑Barré syndrome: Rare autoimmune neuropathy presenting with weakness.
  • Seizures or hypotension: Uncommon neurologic or cardiovascular events that need urgent care.

Precautions & Warnings

Prior to vaccination, certain safety considerations should be observed.

  • Screen for severe allergic reaction: Do not administer to individuals with known hypersensitivity to any vaccine component.
  • Observe after vaccination: Monitor for at least 15 minutes for immediate reactions.
  • Immunocompromised patients: Use with caution in persons with severe immune deficiency; consult a specialist.
  • Pregnancy considerations: Administer only if the potential benefit outweighs the theoretical risk.
  • Store at 2-8°C: Keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Imovax Polio may interact with other medical products, requiring attention to timing and monitoring.

Major Interactions (Avoid)

  • Live viral vaccines: Do not co‑administer with live attenuated vaccines within 4 weeks due to potential interference.
  • Immunoglobulin therapy: Concurrent administration may diminish vaccine immunogenicity.

Moderate Interactions (Monitor Closely)

  • Other inactivated vaccines: May be given concurrently but watch for increased local reactions.
  • Antipyretics: May mask post‑vaccination fever; use as needed.
  • Blood products: May affect antibody response if given within 2 weeks of vaccination.

Frequently Asked Questions

Imovax Polio is an inactivated poliovirus vaccine indicated to prevent poliomyelitis caused by poliovirus types 1, 2 and 3 in children, adolescents and adults. It works by stimulating the immune system to produce protective antibodies before exposure to the virus.

The inactivated poliovirus particles cannot replicate but retain their surface antigens. After intramuscular or subcutaneous injection, antigen‑presenting cells process the viral proteins, leading to activation of B‑cells and production of neutralising antibodies that block infection by each poliovirus serotype.

The dosing schedule is determined by the prescribing health professional based on age, vaccination history and local immunisation guidelines. Typically, a series of injections is given at specific intervals, but the exact amount and timing must be set by the clinician.

Safety data in pregnant or lactating women are limited. The vaccine may be administered if the potential benefit outweighs any theoretical risk, and the decision should be made by a qualified health‑care provider after evaluating the individual’s situation.

Submit an enquiry on the product page at gnhindia.com, specifying 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 options and necessary import documentation.

Imovax Polio is an inactivated poliovirus vaccine (IPV) whereas oral polio vaccine (OPV) contains live attenuated virus. IPV cannot cause vaccine‑derived poliovirus infection and is administered by injection, offering a safer profile in settings where OPV‑related risks are a concern.

The vaccine must be stored refrigerated at 2 °C to 8 °C, protected from light, and must never be frozen or shaken. Vials should be kept in the original packaging until use and inspected for particulate matter before administration.

Imovax Polio is given as an intramuscular or subcutaneous injection, usually in the deltoid muscle of the upper arm or the anterolateral thigh in infants. The injection should be performed by a trained health‑care professional using aseptic technique.

Rare but serious adverse events include severe allergic reactions such as anaphylaxis, Guillain‑Barré syndrome, seizures, and hypotension. Any signs of a serious reaction require immediate medical attention and reporting to pharmacovigilance authorities.

Individuals with a known severe allergy to any component of the vaccine, including the inactivated virus or excipients, should not be vaccinated. Caution is also advised for persons with severe immunodeficiency, and vaccination decisions should be made in consultation with a specialist.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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