🇺🇸 Physioneal 35 in United States

89 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: 89

Most-reported reactions

1. Death — 33 reports (37.08%)
2. Peritonitis Bacterial — 11 reports (12.36%)
3. Cardiac Failure — 9 reports (10.11%)
4. Peritonitis — 9 reports (10.11%)
5. Sepsis — 6 reports (6.74%)
6. Cardiac Arrest — 5 reports (5.62%)
7. Peritoneal Cloudy Effluent — 5 reports (5.62%)
8. Malaise — 4 reports (4.49%)
9. Peritoneal Dialysis Complication — 4 reports (4.49%)
10. Abdominal Pain — 3 reports (3.37%)

Source database →

Frequently asked questions

Is Physioneal 35 approved in United States?

Physioneal 35 does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for Physioneal 35 in United States?

University of Erlangen-Nürnberg Medical School is the originator. The local marketing authorisation holder may differ — check the official source linked above.