🇺🇸 duvie in United States

11 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. Diarrhoea — 2 reports (18.18%)
  2. Abdominal Pain — 1 report (9.09%)
  3. Acute Kidney Injury — 1 report (9.09%)
  4. Asthenia — 1 report (9.09%)
  5. Back Pain — 1 report (9.09%)
  6. Drug Ineffective — 1 report (9.09%)
  7. Gastrointestinal Haemorrhage — 1 report (9.09%)
  8. Ligament Sprain — 1 report (9.09%)
  9. Melaena — 1 report (9.09%)
  10. Myositis — 1 report (9.09%)

Source database →

duvie in other countries

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

Other Metabolic approved in United States

Frequently asked questions

Is duvie approved in United States?

Yes. FDA has authorised it.

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

Pusan National University Hospital is the originator. The local marketing authorisation holder may differ — check the official source linked above.