🇺🇸 Penthotal 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: 28 March 2025 – 28 March 2026
• Total reports: 11

Most-reported reactions

1. Convulsion — 2 reports (18.18%)
2. Acute Kidney Injury — 1 report (9.09%)
3. Agranulocytosis — 1 report (9.09%)
4. Akinesia — 1 report (9.09%)
5. Alanine Aminotransferase Increased — 1 report (9.09%)
6. Aspartate Aminotransferase Increased — 1 report (9.09%)
7. Assisted Suicide — 1 report (9.09%)
8. Bradycardia — 1 report (9.09%)
9. Cytolytic Hepatitis — 1 report (9.09%)
10. Drug Interaction — 1 report (9.09%)

Source database →

Frequently asked questions

Is Penthotal approved in United States?

Penthotal does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for Penthotal in United States?

Rennes University Hospital is the originator. The local marketing authorisation holder may differ — check the official source linked above.