🇺🇸 Vistusertib in United States
11 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: 20 April 2025 – 20 April 2026
- Total reports: 11
Most-reported reactions
- Pyrexia — 2 reports (18.18%)
- Anaemia — 1 report (9.09%)
- Dehydration — 1 report (9.09%)
- Hypoxia — 1 report (9.09%)
- Infarction — 1 report (9.09%)
- Lung Opacity — 1 report (9.09%)
- Nausea — 1 report (9.09%)
- Pneumonia — 1 report (9.09%)
- Psoriasis — 1 report (9.09%)
- Spinal Cord Compression — 1 report (9.09%)
Other Other approved in United States
Frequently asked questions
Is Vistusertib approved in United States?
Vistusertib does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Vistusertib in United States?
Pfizer Inc. is the originator. The local marketing authorisation holder may differ — check the official source linked above.