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Prescribing Information

Before administering TENIVAC vaccine, please see full Prescribing Information.

Reimbursement Information


Tetanus and Diphtheria Toxoids Adsorbed
(Persons 7 years of age and older)

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About TENIVAC Vaccine


TENIVAC vaccine is contraindicated in persons with a known severe allergic reaction (eg, anaphylaxis) after a previous dose of TENIVAC vaccine or any other tetanus- or diphtheria toxoid-containing vaccine or any other component of TENIVAC vaccine. Because of uncertainty as to which component of the vaccine may be responsible, none of the components should be administered.

The tip caps of the prefilled syringes may contain natural rubber latex, which may cause allergic reactions in latex-sensitive individuals.

Persons who experienced an Arthus-type hypersensitivity reaction following a prior dose of tetanus toxoid-containing vaccine should not receive TENIVAC vaccine less than 10 years since the last dose of tetanus toxoid-containing vaccine, even for tetanus prophylaxis as part of wound management.

If Guillain-Barré syndrome has occurred within 6 weeks following previous vaccination with a tetanus toxoid-containing vaccine, the decision to give TENIVAC vaccine should be based on careful consideration of the potential benefits and possible risks.

The most common local and systemic adverse reactions to TENIVAC vaccine include pain, redness, and swelling at the injection site; headache, malaise, muscle weakness, and pain in joints. Other adverse reactions may occur. Vaccination with TENIVAC vaccine may not protect all individuals.


TENIVAC vaccine is indicated for active immunization for prevention of tetanus and diphtheria in persons 7 years of age and older.

Before administering TENIVAC vaccine, please see accompanying full Prescribing Information.


CDC VIS Sheets

Vaccine Information Statement

Guides, Materials, & Brochures


Safety Data Sheet (SDS)

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