Diphtheria and Tetanus Toxoids Adsorbed (diphtheria and tetanus toxoid vaccine manufactured by Sanofi Pasteur.) (Discontinued by the manufacturer in 2023)
- Frequently Reported Adverse Events: In pre-licensure clinical trials, pain, redness, and swelling at the injection site, loss of appetite, crying, and fever. Adverse events were monitored for only 24 hours following vaccination.
- Serious Reported Adverse Events: After licensure (post marketing) adverse event reports have included injection site pain, swelling and hypersensitivity; syncope; convulsion; somnolence; headache; rash; pallor; itching; lymphadenopathy.
