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HSA Product

TETAVAX single dose, suspension for injection in a prefilled syringe

Product approved by Health Sciences Authority (SG)

Basic Information

TETAVAX single dose, suspension for injection in a prefilled syringe

SUSPENSION, STERILE

Regulatory Information

SIN13657P

June 16, 2009

Prescription Only

Therapeutic

SUBCUTANEOUS, INTRAMUSCULAR

August 10, 2023

May 30, 2025

XJ07AM01

Company Information

SANOFI PASTEUR

SANOFI-AVENTIS SINGAPORE PTE. LTD.

SANOFI-AVENTIS SINGAPORE PTE. LTD.

Active Ingredients

Purified Tetanus Toxoid

Strength: 40 I.U. / 0.5ml dose

Detailed Information

Contraindications

**4.3 Contraindications** The lethal risk associated with tetanus excludes any potential contraindication and imposes post-wound exposure prophylaxis In other cases: - Hypersensitivity to one of the ingredients of the vaccine. - Usual contraindications for all vaccinations: vaccination should preferably be postponed in case of fever, acute disease or chronic progressive illness. - Hypersensitivity reaction or neurological disorder after a previous injection of vaccine.

Indication Information

**4.1 Therapeutic Indications** Tetanus prevention and, in particular: - Post-exposure tetanus prophylaxis for recent wounds that may have been contaminated with tetanus spores in subjects who have not had any primary vaccination or for whom primary vaccination is incomplete or uncertain, - Neonatal tetanus prophylaxis in non-immunised women either of childbearing age or pregnant in countries where neonatal tetanus is frequent, - Primary vaccination, - Booster injections.

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