🇺🇸 polyethylene glycol powder in United States

30 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. Death — 6 reports (20%)
  2. Off Label Use — 5 reports (16.67%)
  3. Fall — 4 reports (13.33%)
  4. Dizziness — 3 reports (10%)
  5. Back Pain — 2 reports (6.67%)
  6. Face Injury — 2 reports (6.67%)
  7. Headache — 2 reports (6.67%)
  8. Intestinal Obstruction — 2 reports (6.67%)
  9. Nausea — 2 reports (6.67%)
  10. Pain — 2 reports (6.67%)

Source database →

polyethylene glycol powder 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 polyethylene glycol powder approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for polyethylene glycol powder in United States?

Children's Hospital of Philadelphia is the originator. The local marketing authorisation holder may differ — check the official source linked above.