Transcription of ADT Booster - Medsafe
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ADT Booster Data Sheet Version 7 Page 1 1. PRODUCT NAME ADT Booster . Diphtheria and Tetanus Vaccine (adsorbed) for re-vaccination. 2. QUALITATIVE AND QUANTITATIVE COMPOSITION ADT Booster is a suspension for intramuscular injection, containing aluminium-hydroxide-adsorbed diphtheria and tetanus toxoids. Each dose contains no less than 2 International Units (IU) of purified diphtheria toxoid and no less than 20 IU of purified tetanus toxoid. Each dose of ADT Booster also contains the following excipients: aluminium hydroxide (hydrated) corresponding to mg aluminium, sodium chloride (4 mg), sodium hydroxide to pH 7, and Water for Injections.
Following vaccination with ADT™ Booster, the most common adverse reactions are redness and swelling at the injection site and fever. These reactions most commonly start within 48 hours from the day of vaccination.
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National Immunisation Program Schedule, National Immunisation Program Schedule Queensland, Vaccination, WHO Package insert, World Health Organization, Immunisation, VACCINATION AND IMMUNISATION, VACCINATION AND IMMUNISATION PROGRAMMES 2016, New Zealand Data Sheet, Pertussis vaccines for Australians - NCIRS fact, Pertussis vaccines for Australians | NCIRS Fact, Asked Questions Measles-Rubella, Asked Questions Measles-Rubella Vaccination Campaign, Product Summary File, Immunisation Policy Link to National, Immunisation Policy_____ Link to National