JARDIANCE (empagliflozin) by Boehringer Ingelheim is sodium-glucose transporter 2 inhibitors [moa]. Approved for sodium-glucose cotransporter 2 inhibitor [epc]. First approved in 2014.
Drug data last refreshed 20h ago · AI intelligence enriched 3w ago
JARDIANCE (empagliflozin) is an oral small-molecule sodium-glucose cotransporter 2 (SGLT2) inhibitor approved by the FDA in August 2014. It is indicated for the treatment of type 2 diabetes mellitus and works by inhibiting renal glucose reabsorption, promoting urinary glucose excretion to lower blood glucose levels. The drug has become a cornerstone therapy in diabetes management and is increasingly used for its cardiovascular and renal protective effects beyond glycemic control.
Sodium-Glucose Transporter 2 Inhibitors
Sodium-Glucose Cotransporter 2 Inhibitor
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
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Real-world Study to Describe the Effectiveness and Safety Outcomes of Jardiance in Chinese Patients With Heart Failure and Preserved Ejection Fraction
Effect of Empagliflozin in Patients With eGFR Between 10 and 20 ml/Min/1.73m2
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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JARDIANCE supports roles including brand managers, medical science liaisons, field sales representatives, and health economics specialists focused on diabetes and cardiorenal outcomes messaging. Professionals working on this product require expertise in type 2 diabetes pathophysiology, cardiovascular risk reduction, renal protection mechanisms, and payer/formulary strategy. Currently, zero open positions are linked to this product in the available job tracking data.