🇺🇸 Human fibrinogen concentrate in United States

4 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. Drug Ineffective — 2 reports (50%)
  2. Confusional State — 1 report (25%)
  3. Musculoskeletal Disorder — 1 report (25%)

Source database →

Human fibrinogen concentrate 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 Human fibrinogen concentrate approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Human fibrinogen concentrate in United States?

University Children's Hospital, Zurich is the originator. The local marketing authorisation holder may differ — check the official source linked above.