🇺🇸 parenteral nutrition in United States

661 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: 661

Most-reported reactions

1. Nausea — 83 reports (12.56%)
2. Abdominal Pain — 82 reports (12.41%)
3. Device Related Infection — 73 reports (11.04%)
4. Drug Dose Omission — 72 reports (10.89%)
5. Pyrexia — 70 reports (10.59%)
6. Diarrhoea — 67 reports (10.14%)
7. Vomiting — 66 reports (9.98%)
8. Dehydration — 58 reports (8.77%)
9. Weight Decreased — 46 reports (6.96%)
10. Pneumonia — 44 reports (6.66%)

Source database →

Frequently asked questions

Is parenteral nutrition approved in United States?

parenteral nutrition does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for parenteral nutrition in United States?

Hospices Civils de Lyon is the originator. The local marketing authorisation holder may differ — check the official source linked above.