🇺🇸 VONVENDI in United States

145 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.

Most-reported reactions

  1. No Adverse Event — 42 reports (28.97%)
  2. Drug Ineffective — 16 reports (11.03%)
  3. Haemorrhage — 15 reports (10.34%)
  4. Off Label Use — 14 reports (9.66%)
  5. Haemarthrosis — 11 reports (7.59%)
  6. Product Reconstitution Quality Issue — 11 reports (7.59%)
  7. Epistaxis — 10 reports (6.9%)
  8. Gastrointestinal Haemorrhage — 10 reports (6.9%)
  9. Product Dose Omission Issue — 9 reports (6.21%)
  10. Device Malfunction — 7 reports (4.83%)

Source database →

Other Hematology approved in United States

Frequently asked questions

Is VONVENDI approved in United States?

VONVENDI does not currently have US marketing authorisation in our dataset.

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

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