🇺🇸 VITAMIN K in United States

3,183 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 — 388 reports (12.19%)
  2. Drug Ineffective — 379 reports (11.91%)
  3. Diarrhoea — 362 reports (11.37%)
  4. Off Label Use — 357 reports (11.22%)
  5. Nausea — 354 reports (11.12%)
  6. Dyspnoea — 299 reports (9.39%)
  7. Headache — 278 reports (8.73%)
  8. Pain — 269 reports (8.45%)
  9. Vomiting — 258 reports (8.11%)
  10. Pyrexia — 239 reports (7.51%)

Source database →

VITAMIN K 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 K approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for VITAMIN K in United States?

Marketing authorisation holder not available in our data.