🇺🇸 Medicinal air in United States

13 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: 23 April 2025 – 23 April 2026
• Total reports: 13

Most-reported reactions

1. Foot Fracture — 2 reports (15.38%)
2. Intentional Product Misuse — 2 reports (15.38%)
3. Product Quality Issue — 2 reports (15.38%)
4. Accidental Exposure To Product Packaging — 1 report (7.69%)
5. Cyanosis — 1 report (7.69%)
6. Device Alarm Issue — 1 report (7.69%)
7. Device Connection Issue — 1 report (7.69%)
8. Device Issue — 1 report (7.69%)
9. Fall — 1 report (7.69%)
10. Fibula Fracture — 1 report (7.69%)

Source database →

Frequently asked questions

Is Medicinal air approved in United States?

Medicinal air does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for Medicinal air in United States?

Assistance Publique - Hôpitaux de Paris is the originator. The local marketing authorisation holder may differ — check the official source linked above.