🇺🇸 Air/Oxygen in United States

10 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: 10

Most-reported reactions

1. Abdominal Pain — 1 report (10%)
2. Anaphylactic Reaction — 1 report (10%)
3. Apnoea — 1 report (10%)
4. Bradycardia — 1 report (10%)
5. Diarrhoea — 1 report (10%)
6. Epistaxis — 1 report (10%)
7. Hyperaesthesia — 1 report (10%)
8. Intestinal Perforation — 1 report (10%)
9. Nausea — 1 report (10%)
10. Pneumoperitoneum — 1 report (10%)

Source database →

Frequently asked questions

Is Air/Oxygen approved in United States?

Air/Oxygen does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for Air/Oxygen in United States?

Air Liquide Santé International is the originator. The local marketing authorisation holder may differ — check the official source linked above.