🇺🇸 Chemotherapy in United States

1,190 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. Nausea — 156 reports (13.11%)
  2. Diarrhoea — 147 reports (12.35%)
  3. Drug Ineffective — 144 reports (12.1%)
  4. Dyspnoea — 118 reports (9.92%)
  5. Fatigue — 116 reports (9.75%)
  6. Death — 108 reports (9.08%)
  7. Vomiting — 105 reports (8.82%)
  8. Pyrexia — 104 reports (8.74%)
  9. Asthenia — 101 reports (8.49%)
  10. Pain — 91 reports (7.65%)

Source database →

Chemotherapy 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 Chemotherapy approved in United States?

Yes. FDA has authorised it.

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

Pfizer Inc. is the originator. The local marketing authorisation holder may differ — check the official source linked above.