GNH USA

Europe — EMA

Infanrix Tetra

GNH USA supplies Infanrix Tetra (DTaP‑IPV), a preventive vaccine for diphtheria, tetanus, pertussis and poliomyelitis. Request a quote for global supply.

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

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What is Poliovirus (Inactivated) Type 3 (Saukett Strain), Pertussis Filamentous Haemagglutinin Adsorbed On A?

Diphtheria‑tetanus‑acellular pertussis‑inactivated poliovirus vaccine, the active ingredient in Infanrix Tetra, is a preventive vaccine presented as an injectable solution for intramuscular use. It provides immunization against diphtheria, tetanus, pertussis (whooping cough) and poliomyelitis in infants and young children, following national immunisation schedules. GNH USA supplies Infanrix Tetra as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Poliovirus (Inactivated) Type 3 (Saukett Strain), Pertussis Filamentous Haemagglutinin Adsorbed On A used for?

Infanrix Tetra is a combination vaccine used to prevent bacterial and viral infections targeted by the diphtheria, tetanus, pertussis and poliovirus antigens. - Diphtheria: induces immunity that prevents diphtheria infection and its complications. - Tetanus: stimulates protective antibodies against tetanus toxin, reducing risk of tetanus. - Pertussis (whooping cough): provides immunity to Bordetella pertussis, decreasing incidence of whooping cough. - Poliomyelitis: generates antibodies against poliovirus types, preventing poliomyelitis.

What are the side effects of Poliovirus (Inactivated) Type 3 (Saukett Strain), Pertussis Filamentous Haemagglutinin Adsorbed On A?

Infanrix Tetra, 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. - Fever: low‑grade temperature rise occurring within 24‑48 hours. - Irritability: increased fussiness or crying in infants.

Serious or Rare Side Effects: - Severe allergic reaction (anaphylaxis): rapid onset of hives, airway swelling, or hypotension. - Seizures: rare neurologic events possibly linked to fever. - High‑grade fever: persistent fever above 39°C lasting more than 48 hours.

What precautions apply to Poliovirus (Inactivated) Type 3 (Saukett Strain), Pertussis Filamentous Haemagglutinin Adsorbed On A?

When using Infanrix Tetra, consider the following precautions: - Age restriction: administered only to infants and children according to approved immunisation schedule. - Contraindication: avoid in individuals with known severe allergy to any vaccine component. - Prior reaction: postpone if the child experienced a serious reaction to a previous dose of this vaccine. - Immunocompromised status: consult healthcare provider before vaccinating immunodeficient patients. - Fever or acute illness: defer vaccination until the child has recovered from moderate or severe illness. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Poliovirus (Inactivated) Type 3 (Saukett Strain), Pertussis Filamentous Haemagglutinin Adsorbed On A interact with?

Infanrix Tetra may interact with other medicines or vaccines as follows:

Major Interactions (Avoid): - Live viral vaccines: avoid co‑administration with live attenuated vaccines within 4 weeks due to potential immune interference.

Moderate Interactions (Monitor Closely): - Immunoglobulin therapy: may reduce vaccine immunogenicity; schedule at least 2 weeks apart. - Corticosteroids: high‑dose systemic steroids may blunt antibody response; monitor serology. - Blood products: transfusions may affect vaccine efficacy; consider timing. - Antipyretics: prophylactic use of acetaminophen may slightly diminish antibody titers; use only for symptom relief.

Frequently asked questions

What is Infanrix Tetra used for?+
Infanrix Tetra is a combination vaccine designed to protect infants and young children against four serious diseases: diphtheria, tetanus, pertussis (whooping cough) and poliomyelitis. It is administered as part of routine childhood immunisation programmes to establish long‑term immunity.
How does the active ingredient in Infanrix Tetra work?+
The vaccine contains inactivated diphtheria and tetanus toxoids, acellular pertussis antigens and inactivated poliovirus type 3. After intramuscular injection, these antigens are taken up by antigen‑presenting cells, which trigger B‑cell and T‑cell responses, leading to the production of protective antibodies against each pathogen.
What is the usual dose of Infanrix Tetra?+
The dose and schedule of Infanrix Tetra are determined by the prescribing healthcare professional in accordance with national immunisation guidelines. Typically, the vaccine is given as a series of intramuscular injections during early childhood, but the exact timing is set by the prescriber.
Is Infanrix Tetra safe during pregnancy or breastfeeding?+
Infanrix Tetra is not routinely recommended for use in pregnant women because safety data are limited. Women who are pregnant should receive the vaccine only if the benefits outweigh potential risks, as assessed by a healthcare provider. Limited data suggest that the vaccine is compatible with breastfeeding, but consultation with a clinician is advised.
How do I order Infanrix Tetra from GNH USA?+
To order Infanrix Tetra, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, cold‑chain shipping details and any necessary import documentation.
How does Infanrix Tetra compare with other combination vaccines?+
Infanrix Tetra is comparable to other DTaP‑IPV vaccines such as Pentaxim or Pediacel, offering protection against the same four pathogens. Differences may lie in the specific pertussis antigen composition, the poliovirus strain included, and regulatory approvals. Clinicians choose based on local licensing, supply availability and immunisation schedule preferences.
What are the storage and handling requirements for Infanrix Tetra?+
Infanrix Tetra must be stored refrigerated at 2 °C to 8 °C. It should be kept in the original packaging, protected from light, and must not be frozen or shaken. Maintaining the cold chain during transport and storage is essential to preserve vaccine potency.
How is Infanrix Tetra administered?+
The vaccine is given as an intramuscular injection, usually into the anterolateral thigh of infants or the deltoid muscle of older children. Administration is performed by a qualified healthcare professional using aseptic technique and the appropriate needle size.
What are the most serious risks associated with Infanrix Tetra?+
The most serious adverse events reported are severe allergic reactions (anaphylaxis), seizures, and high‑grade fever persisting beyond 48 hours. These events are rare, but immediate medical attention is required if they occur after vaccination.
Who should not receive Infanrix Tetra?+
Infanrix Tetra should not be given to individuals with a known severe allergy to any component of the vaccine, or to those who have experienced a serious reaction to a previous dose. It should also be deferred in children with moderate or severe acute illness until recovery.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Poliovirus (Inactivated) Type 3 (Saukett Strain), Pertussis Filamentous Haemagglutinin Adsorbed On A
Route
Intramuscular Use
Manufacturer
Glaxosmithkline Biologicals S.A.
Origin
EU

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