🇺🇸 Fluticasone/Formoterol in United States
208 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: 208
Most-reported reactions
- Drug Ineffective — 34 reports (16.35%)
- Asthma — 33 reports (15.87%)
- Drug Intolerance — 24 reports (11.54%)
- Dyspnoea — 24 reports (11.54%)
- Bronchitis — 17 reports (8.17%)
- Obstructive Airways Disorder — 16 reports (7.69%)
- Asthma-Chronic Obstructive Pulmonary Disease Overlap Syndrome — 15 reports (7.21%)
- Breath Sounds Abnormal — 15 reports (7.21%)
- Bronchial Hyperreactivity — 15 reports (7.21%)
- Cardiac Disorder — 15 reports (7.21%)
Other Respiratory/Pulmonology approved in United States
Frequently asked questions
Is Fluticasone/Formoterol approved in United States?
Fluticasone/Formoterol does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Fluticasone/Formoterol in United States?
Mundipharma Korea Ltd is the originator. The local marketing authorisation holder may differ — check the official source linked above.