🇺🇸 Frozen plasma in United States

2,647 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. Renal Failure — 329 reports (12.43%)
  2. Pain — 328 reports (12.39%)
  3. Injury — 304 reports (11.48%)
  4. Unevaluable Event — 296 reports (11.18%)
  5. Anxiety — 273 reports (10.31%)
  6. Fear — 254 reports (9.6%)
  7. Renal Impairment — 240 reports (9.07%)
  8. Renal Injury — 219 reports (8.27%)
  9. Emotional Distress — 210 reports (7.93%)
  10. Stress — 194 reports (7.33%)

Source database →

Frozen plasma 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 Frozen plasma approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Frozen plasma in United States?

Ottawa Hospital Research Institute is the originator. The local marketing authorisation holder may differ — check the official source linked above.