🇺🇸 Vitamin E, Vitamin C in United States

14 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. Atrial Fibrillation — 2 reports (14.29%)
  2. Death — 2 reports (14.29%)
  3. Diarrhoea — 2 reports (14.29%)
  4. Headache — 2 reports (14.29%)
  5. Asthenia — 1 report (7.14%)
  6. Chest Discomfort — 1 report (7.14%)
  7. Chills — 1 report (7.14%)
  8. Colitis — 1 report (7.14%)
  9. Cough — 1 report (7.14%)
  10. Dizziness — 1 report (7.14%)

Source database →

Vitamin E, Vitamin C 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 Vitamin E, Vitamin C approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Vitamin E, Vitamin C in United States?

Sir Takhtasinhji General Hospital is the originator. The local marketing authorisation holder may differ — check the official source linked above.