🇺🇸 Salmeterol MDI 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: 23 April 2025 – 23 April 2026
- Total reports: 10
Most-reported reactions
- Anger — 1 report (10%)
- Asthenia — 1 report (10%)
- Atrophy — 1 report (10%)
- Dysstasia — 1 report (10%)
- Excitability — 1 report (10%)
- Guillain-Barre Syndrome — 1 report (10%)
- Incontinence — 1 report (10%)
- Movement Disorder — 1 report (10%)
- Neuropathy Peripheral — 1 report (10%)
- Palatal Oedema — 1 report (10%)
Other Respiratory approved in United States
Frequently asked questions
Is Salmeterol MDI approved in United States?
Salmeterol MDI does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Salmeterol MDI in United States?
Sumitomo Pharma America, Inc. is the originator. The local marketing authorisation holder may differ — check the official source linked above.