🇺🇸 Dutasteride Capsules in United States

29 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.

Most-reported reactions

  1. Asthenia — 4 reports (13.79%)
  2. Drug Ineffective — 4 reports (13.79%)
  3. Asthma — 3 reports (10.34%)
  4. Blood Count Abnormal — 3 reports (10.34%)
  5. Platelet Count Decreased — 3 reports (10.34%)
  6. Pneumonia — 3 reports (10.34%)
  7. Wheezing — 3 reports (10.34%)
  8. Anaemia — 2 reports (6.9%)
  9. Atrial Fibrillation — 2 reports (6.9%)
  10. Brain Injury — 2 reports (6.9%)

Source database →

Other Urology approved in United States

Frequently asked questions

Is Dutasteride Capsules approved in United States?

Dutasteride Capsules does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for Dutasteride Capsules in United States?

UConn Health is the originator. The local marketing authorisation holder may differ — check the official source linked above.