🇺🇸 Ropinirole (Requip) in United States
31 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: 31
Most-reported reactions
- Dizziness — 4 reports (12.9%)
- Arthralgia — 3 reports (9.68%)
- C-Reactive Protein Increased — 3 reports (9.68%)
- Diarrhoea — 3 reports (9.68%)
- Fatigue — 3 reports (9.68%)
- Malaise — 3 reports (9.68%)
- Muscle Spasms — 3 reports (9.68%)
- Nausea — 3 reports (9.68%)
- Pain — 3 reports (9.68%)
- Vomiting — 3 reports (9.68%)
Other Neurology approved in United States
Frequently asked questions
Is Ropinirole (Requip) approved in United States?
Ropinirole (Requip) does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Ropinirole (Requip) in United States?
St. Luke's-Roosevelt Hospital Center is the originator. The local marketing authorisation holder may differ — check the official source linked above.