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 2 and Type 3, the active ingredient in Imovax Polio, is a vaccine presented as an unspecified strength/vial for intramuscular, subcutaneous use. It prevents poliomyelitis caused by poliovirus types 1, 2, and 3 in individuals at risk.

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 to induce protective immunity against poliovirus infection.

  • Poliomyelitis (polio): Provides active immunity to prevent infection by poliovirus types 1, 2, and 3 in children and adults.
  • Travel to endemic regions: Reduces the risk of poliovirus exposure for travelers visiting areas with ongoing transmission.
  • Outbreak response: Supports mass immunization campaigns to control and eradicate poliovirus spread during public health emergencies.

How It Works

  • Imovax Polio contains chemically inactivated poliovirus antigens of types 1, 2 and 3. After intramuscular or subcutaneous injection, the antigens are taken up by antigen‑presenting cells, processed, and displayed to T‑lymphocytes, which stimulate B‑cell production of neutralising antibodies. The resulting humoral response confers active immunity that blocks viral replication upon future exposure.

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.
  • Fever: low‑grade temperature elevation occurring within 24‑48 hours.
  • Headache: transient headache reported after vaccination.
  • Fatigue: temporary feeling of tiredness.
  • Myalgia: mild muscle aches.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Guillain‑Barré syndrome: rare autoimmune neuropathy that may develop weeks after vaccination.
  • Seizures: infrequent neurologic events, especially in children with pre‑existing conditions.
  • Severe hypotension: marked drop in blood pressure post‑injection.
  • Acute allergic edema: swelling of face, lips, or airway.

Precautions & Warnings

Before administering Imovax Polio, consider the following precautions:

  • Severe allergy: Do not vaccinate individuals with known hypersensitivity to any vaccine component.
  • Acute illness: Postpone vaccination in persons with moderate or severe febrile illness.
  • Immunocompromised status: Evaluate immune function; vaccine may be less effective.
  • Pregnancy: Discuss risk‑benefit with a healthcare professional before use.
  • Breastfeeding: Weigh potential benefits against unknown risks.
  • 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 as follows:

Major Interactions (Avoid)

  • Live attenuated vaccines: Avoid co‑administration within four weeks to prevent interference.
  • Immunoglobulin therapy: May reduce vaccine efficacy if given within two weeks before or after vaccination.
  • Blood products: Concurrent transfusion can impair immune response.

Moderate Interactions (Monitor Closely)

  • Antipyretics (e.g., acetaminophen, ibuprofen): May mask fever but do not affect immunogenicity.
  • Immunosuppressive drugs: May diminish antibody production; monitor serologic response.

Frequently Asked Questions

Imovax Polio is an inactivated poliovirus vaccine indicated for the prevention of poliomyelitis caused by poliovirus types 1, 2, and 3. It is administered to individuals at risk, including children, travelers to endemic areas, and populations targeted in outbreak control campaigns.

The vaccine contains chemically inactivated poliovirus antigens that cannot cause disease. After injection, the antigens are processed by the immune system, prompting B‑cells to produce neutralising antibodies. These antibodies provide active immunity that blocks infection if the person later encounters live poliovirus.

The specific dosing schedule for Imovax Polio is determined by the prescribing healthcare professional based on age, vaccination history, and public health guidelines. The prescriber will set the appropriate number of doses, intervals, and route of administration.

Safety data for Imovax Polio in pregnancy and lactation are limited. Healthcare providers should evaluate the potential benefits against any unknown risks before vaccinating pregnant or breastfeeding individuals. Consultation with a medical professional is essential.

To place an order, submit an enquiry on the Imovax Polio 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 details, and necessary import documentation.

Imovax Polio is an inactivated (killed) poliovirus vaccine, whereas some alternatives are live‑attenuated oral polio vaccines (OPV). Inactivated vaccines cannot cause vaccine‑derived poliovirus infection and are preferred in settings where OPV‑related risks are a concern. Both types aim to induce protective immunity but differ in administration route and storage requirements.

Imovax Polio must be stored refrigerated at 2‑8 °C. Keep the vials in their original packaging, protect them from light, and avoid freezing or shaking. If the cold chain is broken, the vaccine should not be used.

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

Serious adverse events are rare but may include anaphylactic reactions, Guillain‑Barré syndrome, seizures, severe hypotension, and acute allergic edema. Immediate medical attention is required if any of these symptoms occur after vaccination.

Individuals with a known severe allergy to any component of the vaccine, those who have experienced a previous anaphylactic reaction to an inactivated poliovirus vaccine, or persons with acute moderate‑to‑severe febrile illness should not be vaccinated until the condition resolves.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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