🇺🇸 Levonorgestrel IUS in United States

125 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. Drug Ineffective — 25 reports (20%)
  2. Pregnancy With Contraceptive Device — 20 reports (16%)
  3. Device Dislocation — 12 reports (9.6%)
  4. Device Expulsion — 12 reports (9.6%)
  5. Embedded Device — 12 reports (9.6%)
  6. Genital Haemorrhage — 10 reports (8%)
  7. Device Use Issue — 9 reports (7.2%)
  8. Procedural Pain — 9 reports (7.2%)
  9. Abdominal Pain — 8 reports (6.4%)
  10. Medical Device Pain — 8 reports (6.4%)

Source database →

Other Contraception / Gynecology approved in United States

Frequently asked questions

Is Levonorgestrel IUS approved in United States?

Levonorgestrel IUS does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for Levonorgestrel IUS in United States?

Oregon Health and Science University is the originator. The local marketing authorisation holder may differ — check the official source linked above.