🇺🇸 Curare in United States

16 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. Death — 6 reports (37.5%)
  2. Completed Suicide — 2 reports (12.5%)
  3. Acute Respiratory Distress Syndrome — 1 report (6.25%)
  4. Adverse Drug Reaction — 1 report (6.25%)
  5. Adverse Event — 1 report (6.25%)
  6. Anaesthetic Complication — 1 report (6.25%)
  7. Anaphylactic Shock — 1 report (6.25%)
  8. Blood Bilirubin Increased — 1 report (6.25%)
  9. Blood Urea Increased — 1 report (6.25%)
  10. Cerebrovascular Accident — 1 report (6.25%)

Source database →

Other Rare Disease approved in United States

Frequently asked questions

Is Curare approved in United States?

Yes. FDA has authorised it.

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

Centre Hospitalier Universitaire, Amiens is the originator. The local marketing authorisation holder may differ — check the official source linked above.