🇺🇸 inert tablet in United States

39 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: 22 April 2025 – 22 April 2026
• Total reports: 39

Most-reported reactions

1. Drug Ineffective — 6 reports (15.38%)
2. Nausea — 5 reports (12.82%)
3. Pregnancy On Oral Contraceptive — 5 reports (12.82%)
4. Abortion Induced — 4 reports (10.26%)
5. Vomiting — 4 reports (10.26%)
6. Alanine Aminotransferase Increased — 3 reports (7.69%)
7. Deep Vein Thrombosis — 3 reports (7.69%)
8. Drug Interaction — 3 reports (7.69%)
9. Metrorrhagia — 3 reports (7.69%)
10. Unintended Pregnancy — 3 reports (7.69%)

Source database →

Frequently asked questions

Is inert tablet approved in United States?

inert tablet does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for inert tablet in United States?

CMC Ambroise Paré is the originator. The local marketing authorisation holder may differ — check the official source linked above.