🇺🇸 multivitamin in United States

39,953 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 — 6,087 reports (15.24%)
  2. Nausea — 5,179 reports (12.96%)
  3. Drug Ineffective — 4,487 reports (11.23%)
  4. Diarrhoea — 4,481 reports (11.22%)
  5. Headache — 4,207 reports (10.53%)
  6. Dizziness — 3,648 reports (9.13%)
  7. Dyspnoea — 3,201 reports (8.01%)
  8. Pain — 3,078 reports (7.7%)
  9. Asthenia — 2,900 reports (7.26%)
  10. Arthralgia — 2,685 reports (6.72%)

Source database →

multivitamin 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 multivitamin approved in United States?

Yes. FDA has authorised it.

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

New York State Institute for Basic Research is the originator. The local marketing authorisation holder may differ — check the official source linked above.