🇺🇸 Platinum-Based Chemotherapy 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: 22 April 2025 – 22 April 2026
- Total reports: 15
Most-reported reactions
- Malignant Neoplasm Progression — 3 reports (20%)
- Death — 2 reports (13.33%)
- Drug Ineffective — 2 reports (13.33%)
- Nausea — 2 reports (13.33%)
- Abscess — 1 report (6.67%)
- Alopecia — 1 report (6.67%)
- Biliary Obstruction — 1 report (6.67%)
- Carbohydrate Antigen 125 Increased — 1 report (6.67%)
- Condition Aggravated — 1 report (6.67%)
- Decreased Appetite — 1 report (6.67%)
Other Oncology approved in United States
Frequently asked questions
Is Platinum-Based Chemotherapy approved in United States?
Platinum-Based Chemotherapy does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Platinum-Based Chemotherapy in United States?
Genprex, Inc. is the originator. The local marketing authorisation holder may differ — check the official source linked above.