🇺🇸 Doxorubicin hydrochloride liposome in United States
256 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: 256
Most-reported reactions
- Drug Ineffective — 39 reports (15.23%)
- Febrile Neutropenia — 37 reports (14.45%)
- Nausea — 36 reports (14.06%)
- Bone Marrow Failure — 26 reports (10.16%)
- Neutropenia — 26 reports (10.16%)
- Myelosuppression — 20 reports (7.81%)
- Disease Progression — 19 reports (7.42%)
- Vomiting — 19 reports (7.42%)
- Pancytopenia — 17 reports (6.64%)
- Thrombocytopenia — 17 reports (6.64%)
Other Oncology approved in United States
Frequently asked questions
Is Doxorubicin hydrochloride liposome approved in United States?
Doxorubicin hydrochloride liposome does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Doxorubicin hydrochloride liposome in United States?
Shanghai Fudan-Zhangjiang Bio-Pharmaceutical Co., Ltd. is the originator. The local marketing authorisation holder may differ — check the official source linked above.