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HSA Product

VAXIGRIPTETRA SUSPENSION FOR INJECTION IN PREFILLED SYRINGE

Product approved by Health Sciences Authority (SG)

Basic Information

VAXIGRIPTETRA SUSPENSION FOR INJECTION IN PREFILLED SYRINGE

INJECTION, SUSPENSION

Regulatory Information

SIN15477P

May 4, 2018

Prescription Only

Therapeutic

SUBCUTANEOUS, INTRAMUSCULAR

August 10, 2023

May 30, 2025

XJ07BB02

Company Information

SANOFI-AVENTIS SINGAPORE PTE. LTD.

SANOFI-AVENTIS SINGAPORE PTE. LTD.

Active Ingredients

Detailed Information

Contraindications

**4.3. Contraindications** Hypersensitivity to the active substances, to any of the excipients listed in section 6.1 – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_ or to any component that may be present as traces such as eggs (ovalbumin, chicken proteins), neomycin, formaldehyde and octoxinol-9. Vaccination should be postponed in case of moderate or severe febrile disease or acute disease.

Indication Information

**4.1. Therapeutic indications** VaxigripTetra is indicated for the prevention of influenza disease caused by the two influenza A virus subtypes and the two influenza B virus types contained in the vaccine for: - active immunisation of adults, including pregnant women, and children from 6 months of age. The use of VaxigripTetra should be based on official recommendations.

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