🇺🇸 Enteral nutrition in United States

74 US adverse-event reports

Marketing authorisation

FDA

  • Status: approved

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.

Most-reported reactions

  1. Pyrexia — 14 reports (18.92%)
  2. Diarrhoea — 9 reports (12.16%)
  3. Alanine Aminotransferase Increased — 7 reports (9.46%)
  4. Aspartate Aminotransferase Increased — 7 reports (9.46%)
  5. Crohn'S Disease — 7 reports (9.46%)
  6. Drug Ineffective — 7 reports (9.46%)
  7. Anaemia — 6 reports (8.11%)
  8. Intestinal Obstruction — 6 reports (8.11%)
  9. Platelet Count Decreased — 6 reports (8.11%)
  10. Abdominal Pain — 5 reports (6.76%)

Source database →

Enteral nutrition in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Frequently asked questions

Is Enteral nutrition approved in United States?

Yes. FDA has authorised it.

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

Sichuan Cancer Hospital and Research Institute is the originator. The local marketing authorisation holder may differ — check the official source linked above.