🇺🇸 Liquid oxygen in United States

28 US adverse-event reports

Marketing authorisation

FDA

  • Status: approved

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. Accidental Exposure To Product — 5 reports (17.86%)
  2. Respiratory Fume Inhalation Disorder — 4 reports (14.29%)
  3. Malaise — 3 reports (10.71%)
  4. Off Label Use — 3 reports (10.71%)
  5. Respiratory Tract Infection — 3 reports (10.71%)
  6. Asthma — 2 reports (7.14%)
  7. Brain Injury — 2 reports (7.14%)
  8. Chest Discomfort — 2 reports (7.14%)
  9. Chest Pain — 2 reports (7.14%)
  10. Death — 2 reports (7.14%)

Source database →

Liquid oxygen in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Frequently asked questions

Is Liquid oxygen approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Liquid oxygen in United States?

Belfast Health and Social Care Trust is the originator. The local marketing authorisation holder may differ — check the official source linked above.