🇺🇸 dexamedetomidine in United States
12 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: 28 March 2025 – 28 March 2026
- Total reports: 12
Most-reported reactions
- Burkholderia Test Positive — 2 reports (16.67%)
- Recalled Product — 2 reports (16.67%)
- Acinetobacter Test Positive — 1 report (8.33%)
- Acute Respiratory Failure — 1 report (8.33%)
- Atrial Fibrillation — 1 report (8.33%)
- Atrioventricular Block First Degree — 1 report (8.33%)
- Bacteraemia — 1 report (8.33%)
- Blood Creatine Phosphokinase Increased — 1 report (8.33%)
- Blood Culture Positive — 1 report (8.33%)
- Blood Pressure Decreased — 1 report (8.33%)
Other Other approved in United States
Frequently asked questions
Is dexamedetomidine approved in United States?
dexamedetomidine does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for dexamedetomidine in United States?
Assiut University is the originator. The local marketing authorisation holder may differ — check the official source linked above.