🇺🇸 TETANUS TOXOID in United States

799 US adverse-event reports

Marketing authorisation

FDA

  • Status: approved

Safety signals — FAERS

Adverse reaction reports describe suspected side effects. A report does not mean the drug caused the event — co-medications, underlying disease and coincidence all contribute.

Most-reported reactions

  1. Drug Hypersensitivity — 181 reports (22.65%)
  2. Pain — 81 reports (10.14%)
  3. Fatigue — 73 reports (9.14%)
  4. Maternal Exposure During Pregnancy — 69 reports (8.64%)
  5. Pyrexia — 69 reports (8.64%)
  6. Diarrhoea — 68 reports (8.51%)
  7. Foetal Exposure During Pregnancy — 67 reports (8.39%)
  8. Arthralgia — 65 reports (8.14%)
  9. Drug Ineffective — 63 reports (7.88%)
  10. Nausea — 63 reports (7.88%)

Source database →

TETANUS TOXOID in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Frequently asked questions

Is TETANUS TOXOID approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for TETANUS TOXOID in United States?

Marketing authorisation holder not available in our data.