AGREES TO SETTLE A LARGE NUMBER OF INVOKANA® LAWSUITS
Many of those who were prescribed Invokana® or other SGLT2 inhibitor for the treatment of their Type 2 diabetes have suffered severe adverse side effects as a result of taking the drug. Because Invokana® functions through the kidneys, patients who take the drug may experience significant dehydration, which can lead to dangerous consequences especially in those with diabetes.
This dehydration can compromise blood flow to the arms, legs, and feet. For many patients suffering from diabetes, limited blood flow could lead to amputations. In 2016, the FDA responded to these adverse effects by issuing a warning regarding the effects of the drug through research that was conducted.
FDA APPROVES INVOKANA® FOR TYPE 2 DIABETES TREATMENT –
FDA IS NOTIFIED OF 450 ADVERSE EVENTS LINKED TO INVOKANA® –
WARNING ISSUED BY FDA TO THE PUBLIC REGARDING INVOKANA® –
FDA ISSUES "BLACK BOX" WARNING FOR INVOKANA® –
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