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) and Poliovirus (Inactivated) Type 2 (Mef-1 Strain), the active ingredient in Imovax Polio, is a vaccine presented as an injectable solution for intramuscular or subcutaneous use. It prevents poliomyelitis by inducing immunity against poliovirus types 2 and 3.

GNH India supplies Imovax Polio as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Sanofi Winthrop Industrie

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Indications & Clinical Uses

Imovax Polio is an inactivated poliovirus vaccine used in the prevention of poliomyelitis.

  • Poliomyelitis: Provides active immunity that protects against infection with poliovirus types 2 and 3.
  • Travel to endemic regions: Reduces the risk of acquiring poliovirus during international travel.
  • Outbreak response: Supports mass‑immunisation campaigns aimed at controlling poliovirus outbreaks.

How It Works

  • Imovax Polio contains chemically inactivated poliovirus antigens of types 2 and 3. After intramuscular or subcutaneous injection, the antigens are taken up by antigen‑presenting cells, which display them to helper T cells. This triggers B‑cell activation and the production of neutralising antibodies that specifically bind poliovirus, preventing viral replication and disease.

Side Effects

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the site of administration.
  • Redness or swelling: localized erythema or edema that resolves within a few days.
  • Low‑grade fever: transient elevation of body temperature.
  • Headache: mild headache occurring within 24 hours.
  • Fatigue: temporary tiredness after vaccination.
  • Muscle aches: mild myalgia at the injection site.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Guillain‑Barré syndrome: rare neurological disorder presenting with muscle weakness.
  • Seizures: uncommon convulsive episodes.
  • Severe hypotension: marked drop in blood pressure post‑injection.
  • Extensive rash or urticaria: widespread skin eruption.
  • Encephalitis: extremely rare inflammation of the brain.

Precautions & Warnings

Before administering Imovax Polio, consider the following precautions:

  • Allergy screening: avoid use in individuals with severe hypersensitivity to any vaccine component.
  • Pregnancy: consult a healthcare provider; limited safety data are available.
  • Immunocompromised patients: vaccine may elicit a reduced immune response.
  • Concomitant vaccines: follow recommended immunisation schedules to avoid interference.
  • Post‑vaccination observation: monitor for immediate adverse reactions for at least 15 minutes.
  • Store at 2‑8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Imovax Polio may interact with other agents as follows:

Major Interactions (Avoid)

  • Live viral vaccines: avoid simultaneous administration to prevent immune interference.
  • Immunoglobulin therapy: may diminish vaccine‑induced antibody response.
  • Blood products: can reduce immunogenicity if given shortly before or after vaccination.

Moderate Interactions (Monitor Closely)

  • Antipyretics (e.g., acetaminophen, ibuprofen): may mask fever, a sign of reaction.
  • Immunosuppressive drugs: may lower the effectiveness of the vaccine and require serologic monitoring.

Frequently Asked Questions

Imovax Polio is an inactivated poliovirus vaccine indicated for the prevention of poliomyelitis. It is administered to individuals to develop protective immunity against poliovirus types 2 and 3, reducing the risk of infection and disease.

The vaccine contains chemically inactivated poliovirus antigens that cannot cause disease. When injected, these antigens are processed by the immune system, prompting the production of neutralising antibodies that specifically target poliovirus, thereby preventing viral replication if exposure occurs.

The dosage and schedule of Imovax Polio are determined by the prescribing healthcare professional based on age, vaccination history, and local immunisation guidelines. The prescriber will set the appropriate dose and timing for each patient.

Safety data for Imovax Polio in pregnancy are limited. Healthcare providers should weigh the potential benefits against any unknown risks. The vaccine is not known to be excreted in breast milk, but a clinician’s advice is recommended before vaccination during lactation.

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

Imovax Polio is an inactivated (killed) poliovirus vaccine, whereas oral polio vaccine (OPV) contains live attenuated virus. Inactivated vaccines cannot cause vaccine‑derived poliovirus infection and are preferred in settings where OPV‑related risks must be avoided, such as in immunocompromised individuals.

Imovax Polio must be stored at 2‑8 °C (refrigerated). Keep the vials in the original packaging, protect them from light, and do not freeze or shake the solution. Follow cold‑chain procedures during transport to maintain potency.

The vaccine is given by a healthcare professional as an intramuscular or subcutaneous injection, typically in the deltoid muscle or the anterolateral thigh in infants. The injection site should be cleaned with an antiseptic before administration.

Serious adverse events are rare but may include anaphylactic reactions, Guillain‑Barré syndrome, seizures, severe hypotension, extensive rash, or encephalitis. Immediate medical attention is required if any of these symptoms develop after vaccination.

Individuals with a known severe allergy to any component of the vaccine should not receive it. Those who have experienced a previous severe reaction to an inactivated poliovirus vaccine should also avoid it. Consultation with a healthcare provider is essential for other special populations.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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