Product image of Infanrix-Ipv (Poliovirus (Inactivated) Type 3 (Saukett Strain), Pertussis Filamentous Haemagglutinin Adsorbed On A) supplied by GNH India

Infanrix-Ipv

Active Ingredient:
Poliovirus (Inactivated) Type 3 (Saukett Strain), Pertussis Filamentous Haemagglutinin Adsorbed On A
Origin:
EU

Infanrix-Ipv (Poliovirus (Inactivated) Type 3 (Saukett Strain), Pertussis Filamentous Haemagglutinin Adsorbed On A)

Poliovirus type 3 (inactivated), the active ingredient in Infanrix-Ipv, is a vaccine presented as a sterile injectable for intramuscular use. It induces immunity to prevent poliomyelitis caused by poliovirus type 3 and protects against pertussis in infants and children. It is incorporated into routine childhood immunisation programmes to provide combined protection.

GNH India supplies Infanrix-Ipv as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies, and clinics worldwide, ensuring quality and regulatory compliance across global markets. The company adheres to stringent cold‑chain logistics to maintain vaccine potency during transport and storage.

Manufacturer / TM Owner

Glaxosmithkline, S.A.

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Indications & Clinical Uses

Infanrix-Ipv is a combination vaccine that targets viral and bacterial pathogens responsible for poliomyelitis type 3 and pertussis.

  • Poliomyelitis type 3: Provides active immunity to prevent infection with poliovirus type 3 in infants and young children.
  • Pertussis (whooping cough): Induces protective antibodies against pertussis filamentous haemagglutinin to reduce incidence of whooping cough.
  • Combined immunisation schedule: Facilitates inclusion in routine childhood vaccination programs, simplifying protection against both diseases.

How It Works

  • Infanrix-Ipv contains inactivated poliovirus type 3 particles and purified pertussis filamentous haemagglutinin adsorbed onto an adjuvant. After intramuscular injection, antigen‑presenting cells process the viral capsid proteins and bacterial haemagglutinin, presenting them to T‑cells. This stimulates B‑cell activation and production of neutralising antibodies against poliovirus and pertussis antigens, establishing active humoral immunity. The generated memory B‑cells enable rapid response upon future exposure, while helper T‑cells support the antibody response.

Side Effects

Infanrix-Ipv, like other injectable vaccines, may be associated with local and systemic reactions.

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Redness or swelling: localized erythema or edema that resolves within a few days.
  • Low‑grade fever: temperature rise up to 38 °C occurring within 24‑48 hours.
  • Irritability or fussiness: especially in infants after vaccination.
  • Headache: transient mild headache reported by some recipients.

Serious or Rare Side Effects

  • Anaphylactic reaction: severe allergic response requiring immediate medical attention.
  • Seizures: febrile seizures associated with high fever post‑vaccination.
  • Persistent high fever: temperature above 39 °C lasting more than 48 hours.
  • Apnea in young infants: brief pauses in breathing observed rarely.
  • Guillain‑Barré syndrome: extremely rare demyelinating neuropathy reported post‑immunisation.

Precautions & Warnings

Before administering Infanrix-Ipv, healthcare professionals should observe several precautionary measures.

  • Contraindication: Do not vaccinate individuals with a documented severe allergic reaction to any vaccine component.
  • Acute illness: Postpone vaccination if the patient has a moderate or severe febrile illness.
  • Immunocompromised status: Evaluate risks in severely immunocompromised patients, although the vaccine is inactivated.
  • Pregnancy: Use only if the benefit outweighs potential risk, following professional guidance.
  • Monitoring: Observe the patient for at least 15 minutes after injection for signs of anaphylaxis.
  • Store at 2-8°C: Keep refrigerated, protect from light, do not freeze or shake the vial.

Avoid Interactions

Infanrix-Ipv may interact with other medical products; awareness of potential interactions is important.

Major Interactions (Avoid)

  • Live viral vaccines: Avoid simultaneous administration with live attenuated vaccines such as measles‑mumps‑rubella, as it may reduce immune response.
  • Immunoglobulin therapy: Do not give within 2 weeks of immune globulin, which can interfere with antibody development.

Moderate Interactions (Monitor Closely)

  • Other inactivated vaccines: Co‑administration is generally acceptable but monitor for increased reactogenicity.
  • Antipyretics: Use of prophylactic acetaminophen may blunt antibody response; consider timing.
  • Corticosteroids: High‑dose steroids may diminish vaccine efficacy; assess patient’s steroid regimen.

Frequently Asked Questions

Infanrix-Ipv is a combination vaccine indicated for the prevention of poliomyelitis caused by poliovirus type 3 and for protection against pertussis (whooping cough) in infants and young children as part of routine immunisation schedules.

The inactivated poliovirus type 3 particles in Infanrix-Ipv are unable to cause disease but retain their antigenic structure. After intramuscular injection, they are taken up by antigen‑presenting cells, which trigger a T‑cell‑dependent immune response, leading to the production of neutralising antibodies that block future poliovirus infection.

The dosing schedule for Infanrix-Ipv is determined by the prescribing healthcare professional based on national immunisation guidelines and the patient’s age. The regimen typically involves a series of primary doses followed by booster(s), but exact timing and number of doses should be confirmed by the clinician.

Safety data for Infanrix-Ipv in pregnancy are limited; it should only be administered when the potential benefit to the mother or fetus outweighs any theoretical risk, following professional medical advice. Breastfeeding is not a contraindication, but mothers should discuss vaccination with their healthcare provider.

To order Infanrix-Ipv, 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 details, and necessary import documentation.

Infanrix-Ipv combines inactivated poliovirus type 3 and pertussis filamentous haemagglutinin into a single injection, reducing the number of visits and needle sticks compared with administering separate polio and pertussis vaccines. Immunogenicity and safety profiles are comparable, while the combined formulation offers logistical convenience for immunisation programmes.

Infanrix-Ipv must be stored at 2 °C to 8 °C in a refrigerator. The vial should be kept in its original packaging, protected from light, and must not be frozen or shaken. Maintaining the cold chain during transport and storage preserves vaccine potency.

Infanrix-Ipv is given by a single intramuscular injection, usually into the anterolateral thigh in infants or the deltoid muscle in older children. The injection should be performed by a qualified healthcare professional using aseptic technique, and the patient should be observed briefly after administration.

The most serious risks, although rare, include severe allergic reactions such as anaphylaxis, febrile seizures triggered by high fever, and, very rarely, neurological conditions like Guillain‑Barré syndrome. Immediate medical attention is required if any signs of a serious reaction appear after vaccination.

Infanrix-Ipv should not be given to individuals with a known severe allergy to any component of the vaccine, or to those who have experienced a previous anaphylactic reaction to a poliovirus or pertussis vaccine. It should also be deferred in patients with acute moderate or severe illness until recovery.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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