🇺🇸 Losartan and Amlodipine in United States
12 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: 12
Most-reported reactions
- Intentional Overdose — 2 reports (16.67%)
- Shock — 2 reports (16.67%)
- Cataract — 1 report (8.33%)
- Extra Dose Administered — 1 report (8.33%)
- Headache — 1 report (8.33%)
- Hip Fracture — 1 report (8.33%)
- Limb Injury — 1 report (8.33%)
- Nervousness — 1 report (8.33%)
- Product Quality Issue — 1 report (8.33%)
- Radiculopathy — 1 report (8.33%)
Other Cardiovascular approved in United States
Frequently asked questions
Is Losartan and Amlodipine approved in United States?
Losartan and Amlodipine does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Losartan and Amlodipine in United States?
Centro Universitario de Ciencias de la Salud, Mexico is the originator. The local marketing authorisation holder may differ — check the official source linked above.