🇺🇸 Vitamin D3 in United States

114,754 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 — 18,634 reports (16.24%)
  2. Diarrhoea — 12,734 reports (11.1%)
  3. Nausea — 12,722 reports (11.09%)
  4. Headache — 11,740 reports (10.23%)
  5. Drug Ineffective — 11,116 reports (9.69%)
  6. Pain — 10,737 reports (9.36%)
  7. Off Label Use — 10,331 reports (9%)
  8. Dizziness — 9,078 reports (7.91%)
  9. Dyspnoea — 8,911 reports (7.77%)
  10. Arthralgia — 8,751 reports (7.63%)

Source database →

Vitamin D3 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 D3 approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Vitamin D3 in United States?

Prisma Health-Midlands is the originator. The local marketing authorisation holder may differ — check the official source linked above.