🇺🇸 Mitozantrone in United States
15 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: 28 March 2025 – 28 March 2026
- Total reports: 15
Most-reported reactions
- Myelodysplastic Syndrome — 3 reports (20%)
- Neutropenia — 2 reports (13.33%)
- Neutropenic Sepsis — 2 reports (13.33%)
- Pancytopenia — 2 reports (13.33%)
- Acute Leukaemia — 1 report (6.67%)
- Ascites — 1 report (6.67%)
- Ataxia — 1 report (6.67%)
- Atrial Fibrillation — 1 report (6.67%)
- B-Cell Lymphoma — 1 report (6.67%)
- Bone Marrow Failure — 1 report (6.67%)
Other Oncology approved in United States
Frequently asked questions
Is Mitozantrone approved in United States?
Mitozantrone does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Mitozantrone in United States?
US Department of Veterans Affairs is the originator. The local marketing authorisation holder may differ — check the official source linked above.