🇺🇸 vitamin A and E in United States

11 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. Infection — 2 reports (18.18%)
  2. Application Site Pain — 1 report (9.09%)
  3. Back Pain — 1 report (9.09%)
  4. Bone Pain — 1 report (9.09%)
  5. Cataract — 1 report (9.09%)
  6. Chronic Sinusitis — 1 report (9.09%)
  7. Constipation — 1 report (9.09%)
  8. Dizziness — 1 report (9.09%)
  9. Dyskinesia — 1 report (9.09%)
  10. Ear Pain — 1 report (9.09%)

Source database →

vitamin A and E 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 A and E approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for vitamin A and E in United States?

Cairo University is the originator. The local marketing authorisation holder may differ — check the official source linked above.