Drug Landscape ›
Empagliflozin Tablets ›
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: 11
Most-reported reactions
Diarrhoea — 2 reports (18.18%) Blood Glucose Fluctuation — 1 report (9.09%) Blood Glucose Increased — 1 report (9.09%) Cardiac Failure — 1 report (9.09%) Gastritis Erosive — 1 report (9.09%) Gastrooesophageal Reflux Disease — 1 report (9.09%) Glycosylated Haemoglobin Increased — 1 report (9.09%) Lipase Increased — 1 report (9.09%) Magnetic Resonance Imaging Abnormal — 1 report (9.09%) Oesophagitis — 1 report (9.09%)
Source database →
Empagliflozin Tablets 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 Empagliflozin Tablets approved in United States?
Yes. FDA has authorised it.
Who is the marketing authorisation holder for Empagliflozin Tablets in United States?
Kobe University is the originator. The local marketing authorisation holder may differ — check the official source linked above.