🇺🇸 Amlodipine+Benazepril in United States
680 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: 680
Most-reported reactions
- Fatigue — 104 reports (15.29%)
- Drug Ineffective — 89 reports (13.09%)
- Nausea — 87 reports (12.79%)
- Diarrhoea — 83 reports (12.21%)
- Dizziness — 59 reports (8.68%)
- Headache — 57 reports (8.38%)
- Completed Suicide — 54 reports (7.94%)
- Dyspnoea — 54 reports (7.94%)
- Pain — 47 reports (6.91%)
- Arthralgia — 46 reports (6.76%)
Other Cardiovascular approved in United States
Frequently asked questions
Is Amlodipine+Benazepril approved in United States?
Amlodipine+Benazepril does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Amlodipine+Benazepril in United States?
TSH Biopharm Corporation Limited is the originator. The local marketing authorisation holder may differ — check the official source linked above.