🇺🇸 drug administration in United States

10 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. Abdominal Pain — 1 report (10%)
  2. Anaemia — 1 report (10%)
  3. Aplasia — 1 report (10%)
  4. Asthenia — 1 report (10%)
  5. Colorectal Cancer Recurrent — 1 report (10%)
  6. Death — 1 report (10%)
  7. Dehydration — 1 report (10%)
  8. Depressed Level Of Consciousness — 1 report (10%)
  9. Dermatitis Acneiform — 1 report (10%)
  10. Diarrhoea — 1 report (10%)

Source database →

drug administration 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 drug administration approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for drug administration in United States?

Centre hospitalier de l'Université de Montréal (CHUM) is the originator. The local marketing authorisation holder may differ — check the official source linked above.