🇺🇸 Propess in United States

241 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. Caesarean Section — 44 reports (18.26%)
  2. Foetal Exposure During Pregnancy — 30 reports (12.45%)
  3. Drug Exposure During Pregnancy — 28 reports (11.62%)
  4. Postpartum Haemorrhage — 26 reports (10.79%)
  5. Small For Dates Baby — 25 reports (10.37%)
  6. Premature Separation Of Placenta — 20 reports (8.3%)
  7. Uterine Hypertonus — 19 reports (7.88%)
  8. Exposure During Pregnancy — 17 reports (7.05%)
  9. Foetal Death — 17 reports (7.05%)
  10. Death Neonatal — 15 reports (6.22%)

Source database →

Other Other approved in United States

Frequently asked questions

Is Propess approved in United States?

Propess does not currently have US marketing authorisation in our dataset.

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

Ain Shams University is the originator. The local marketing authorisation holder may differ — check the official source linked above.