🇺🇸 Org 36286 in United States

16 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.

• Window: 28 March 2025 – 28 March 2026
• Total reports: 16

Most-reported reactions

1. Ectopic Pregnancy — 6 reports (37.5%)
2. Drug Exposure Before Pregnancy — 2 reports (12.5%)
3. Abdominal Pain Lower — 1 report (6.25%)
4. Drug Exposure During Pregnancy — 1 report (6.25%)
5. Heterotopic Pregnancy — 1 report (6.25%)
6. Metrorrhagia — 1 report (6.25%)
7. Nausea — 1 report (6.25%)
8. Ruptured Ectopic Pregnancy — 1 report (6.25%)
9. Uterine Spasm — 1 report (6.25%)
10. Vaginal Haemorrhage — 1 report (6.25%)

Source database →

Frequently asked questions

Is Org 36286 approved in United States?

Org 36286 does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for Org 36286 in United States?

Organon and Co is the originator. The local marketing authorisation holder may differ — check the official source linked above.