🇺🇸 Coagulation Factor VIII in United States
488 US adverse-event reports
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.
- Window: 22 April 2025 – 22 April 2026
- Total reports: 488
Most-reported reactions
- Haemorrhage — 150 reports (30.74%)
- Drug Ineffective — 111 reports (22.75%)
- Haemarthrosis — 45 reports (9.22%)
- Factor Viii Inhibition — 40 reports (8.2%)
- Dyspnoea — 26 reports (5.33%)
- Anaphylactic Reaction — 25 reports (5.12%)
- Epistaxis — 23 reports (4.71%)
- Fall — 23 reports (4.71%)
- Pain — 23 reports (4.71%)
- Contusion — 22 reports (4.51%)
Other Hematology approved in United States
Frequently asked questions
Is Coagulation Factor VIII approved in United States?
Coagulation Factor VIII does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Coagulation Factor VIII in United States?
Beijing Children's Hospital is the originator. The local marketing authorisation holder may differ — check the official source linked above.