🇺🇸 Enfortumab Vedotin-Ejfv in United States
320 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: 23 April 2025 – 23 April 2026
- Total reports: 320
Most-reported reactions
- Death — 38 reports (11.88%)
- Fatigue — 38 reports (11.88%)
- Inappropriate Schedule Of Product Administration — 35 reports (10.94%)
- Rash — 34 reports (10.62%)
- Diarrhoea — 33 reports (10.31%)
- Nausea — 32 reports (10%)
- Neuropathy Peripheral — 32 reports (10%)
- Decreased Appetite — 31 reports (9.69%)
- Pruritus — 24 reports (7.5%)
- Alopecia — 23 reports (7.19%)
Other Oncology approved in United States
Frequently asked questions
Is Enfortumab Vedotin-Ejfv approved in United States?
Enfortumab Vedotin-Ejfv does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Enfortumab Vedotin-Ejfv in United States?
Mirati Therapeutics Inc. is the originator. The local marketing authorisation holder may differ — check the official source linked above.