🇺🇸 Cisplatin, paclitaxel in United States
36 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: 36
Most-reported reactions
- Second Primary Malignancy — 6 reports (16.67%)
- White Blood Cell Count Increased — 6 reports (16.67%)
- Acute Monocytic Leukaemia — 4 reports (11.11%)
- Malignant Neoplasm Progression — 4 reports (11.11%)
- Hypoglycaemia — 3 reports (8.33%)
- Ill-Defined Disorder — 3 reports (8.33%)
- Metastases To Lymph Nodes — 3 reports (8.33%)
- Pain — 3 reports (8.33%)
- Acute Myeloid Leukaemia — 2 reports (5.56%)
- Acute Myelomonocytic Leukaemia — 2 reports (5.56%)
Other Oncology approved in United States
Frequently asked questions
Is Cisplatin, paclitaxel approved in United States?
Cisplatin, paclitaxel does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Cisplatin, paclitaxel in United States?
Karolinska University Hospital is the originator. The local marketing authorisation holder may differ — check the official source linked above.