🇺🇸 multivitamins in United States

17,017 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. Fatigue — 2,727 reports (16.03%)
  2. Diarrhoea — 2,130 reports (12.52%)
  3. Drug Ineffective — 2,069 reports (12.16%)
  4. Nausea — 2,015 reports (11.84%)
  5. Headache — 1,661 reports (9.76%)
  6. Dizziness — 1,494 reports (8.78%)
  7. Pain — 1,354 reports (7.96%)
  8. Dyspnoea — 1,242 reports (7.3%)
  9. Rash — 1,178 reports (6.92%)
  10. Pneumonia — 1,147 reports (6.74%)

Source database →

multivitamins in other countries

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

Other Other approved in United States

Frequently asked questions

Is multivitamins approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for multivitamins in United States?

Faculdade de Medicina do ABC is the originator. The local marketing authorisation holder may differ — check the official source linked above.