Drug Landscape ›
valsartan plus hydrochlorothiazide ›
Regulatory · United States
Marketing authorisation
FDA
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: 20 April 2025 – 20 April 2026
Total reports: 10
Most-reported reactions
Back Pain — 1 report (10%) Bladder Cancer — 1 report (10%) Bladder Transitional Cell Carcinoma — 1 report (10%) Bladder Transitional Cell Carcinoma Recurrent — 1 report (10%) Dehydration — 1 report (10%) Drug Interaction — 1 report (10%) Drug Level Increased — 1 report (10%) Erythema — 1 report (10%) Feeling Hot — 1 report (10%) Foetal Exposure During Pregnancy — 1 report (10%)
Source database →
valsartan plus hydrochlorothiazide in other countries
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Frequently asked questions
Is valsartan plus hydrochlorothiazide approved in United States?
Yes. FDA has authorised it.
Who is the marketing authorisation holder for valsartan plus hydrochlorothiazide in United States?
Novartis is the originator. The local marketing authorisation holder may differ — check the official source linked above.