🇺🇸 Prontosan in United States

37 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: 37

Most-reported reactions

1. Loss Of Consciousness — 5 reports (13.51%)
2. Sepsis — 5 reports (13.51%)
3. Neutropenia — 4 reports (10.81%)
4. Pyrexia — 4 reports (10.81%)
5. Suicidal Ideation — 4 reports (10.81%)
6. Acute Kidney Injury — 3 reports (8.11%)
7. Acute Psychosis — 3 reports (8.11%)
8. Agitated Depression — 3 reports (8.11%)
9. Anaphylactic Reaction — 3 reports (8.11%)
10. Confusional State — 3 reports (8.11%)

Source database →

Frequently asked questions

Is Prontosan approved in United States?

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

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

Consorci Sanitari de l'Alt Penedès i Garraf is the originator. The local marketing authorisation holder may differ — check the official source linked above.