🇺🇸 Moxifloxacin (Avelox) 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
- Abdominal Pain Upper — 1 report (10%)
- Cardiac Arrest — 1 report (10%)
- Central Nervous System Lesion — 1 report (10%)
- Clostridium Difficile Infection — 1 report (10%)
- Discomfort — 1 report (10%)
- Dizziness — 1 report (10%)
- Dyspnoea — 1 report (10%)
- Dyspnoea Exertional — 1 report (10%)
- Haemoglobin Decreased — 1 report (10%)
- Haemorrhage — 1 report (10%)
Other Infectious Disease approved in United States
Frequently asked questions
Is Moxifloxacin (Avelox) approved in United States?
Moxifloxacin (Avelox) does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Moxifloxacin (Avelox) in United States?
Connect Biopharma Australia Pty Ltd is the originator. The local marketing authorisation holder may differ — check the official source linked above.