
FDA approves Synjardy for type 2 diabetes
FDA has approved empagliflozin and metformin hydrochloride (Synjardy, Boehringer Ingelheim Pharmaceuticals, Inc. and Eli Lilly and Company) tablets for the treatment of adults with type 2 diabetes.
FDA has approved empagliflozin and metformin hydrochloride (Synjardy,
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Diabetes is a metabolic condition that occurs because of the body’s inability to either produce or use the hormone, insulin, which leads to high blood glucose levels. An estimated 29 million Americans currently have type 1 diabetes (T1D) or T2D. T2D, a condition in which the body does not utilize insulin properly, is the most common type, accounting for approximately 90% to 95% of all diagnosed adult diabetes patients in the United States.
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Synjardy is indicated as an adjunct to diet and exercise to improve glycemic control in adults with T2D who are not adequately controlled on a regimen containing empagliflozin or metformin, or in patients already being treated with empagliflozin and metformin as separate medications. The FDA approval of Synjardy was based on results from multiple clinical trials examining the co-administration of empagliflozin and metformin, alone or in combination with a sulfonylurea, in the treatment of T2D.
"Synjardy is now the fifth FDA-approved medicine to emerge from the
The most common side effects associated with the use of Synjardy include stuffy or runny nose and sore throat, urinary tract infections, diarrhea, headache, nausea and vomiting. Synjardy’s label does contain a boxed warning as metformin can cause lactic acidosis, a rare but potentially fatal metabolic complication. Synjardy is not for the treatment of T1D or diabetic ketoacidosis.
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