🇺🇸 Paclitaxel and carboplatin in United States
10 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: 10
Most-reported reactions
- Arthritis — 1 report (10%)
- Cervix Carcinoma Stage Iv — 1 report (10%)
- Chronic Obstructive Pulmonary Disease — 1 report (10%)
- Diabetes Mellitus — 1 report (10%)
- Gastrooesophageal Reflux Disease — 1 report (10%)
- Metastases To Lung — 1 report (10%)
- Migraine — 1 report (10%)
- Neutropenia — 1 report (10%)
- Neutrophil Count Decreased — 1 report (10%)
- Peripheral Vascular Disorder — 1 report (10%)
Other Oncology approved in United States
Frequently asked questions
Is Paclitaxel and carboplatin approved in United States?
Paclitaxel and carboplatin does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Paclitaxel and carboplatin in United States?
Chinese Academy of Medical Sciences is the originator. The local marketing authorisation holder may differ — check the official source linked above.