🇺🇸 Levodopa/carbidopa/entacapone in United States
161 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: 161
Most-reported reactions
- Fall — 23 reports (14.29%)
- Drug Ineffective — 21 reports (13.04%)
- Dyskinesia — 21 reports (13.04%)
- Parkinson^S Disease — 20 reports (12.42%)
- Hallucination, Visual — 14 reports (8.7%)
- Gait Disturbance — 13 reports (8.07%)
- Weight Decreased — 13 reports (8.07%)
- Mobility Decreased — 12 reports (7.45%)
- On And Off Phenomenon — 12 reports (7.45%)
- Pneumonia — 12 reports (7.45%)
Other Neurology approved in United States
Frequently asked questions
Is Levodopa/carbidopa/entacapone approved in United States?
Levodopa/carbidopa/entacapone does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Levodopa/carbidopa/entacapone in United States?
Novartis is the originator. The local marketing authorisation holder may differ — check the official source linked above.