Avandia Information Center: __________________ Avandia Alert FDA’s Evaluation of AVANDIA Injured by Avandia? 'Black Box' Warning for Avandia

The American Heart Association and American Diabetes Association have issued recommendations to guide the use of Avandia. Diabetics who have mild heart disease or any problems with their kidneys may be at an increased risk of developing congestive heart failure if they take certain diabetes medications. The study, published in the September 9, 2003 issue of the Mayo Clinic Proceedings, reported on 6 cases of congestive heart failure in people taking Avandia. The researchers studied the records of six men, between the ages of 66 and 78 years, with Type-II diabetes. All six patients complained of shortness of breath, swelling of their feet, and weight gain, which are symptoms of congestive heart failure and pulmonary edema (fluid buildup in the lungs). Congestive heart failure occurs when the heart can no longer pump enough blood to maintain adequate circulation. Because the heart doesn't pump properly, fluid often builds up in the lungs.

Four of the six people in this study had chronic renal insufficiency, which means that their kidneys weren't functioning normally. Only two had any previous signs of heart disease. Four of the six had high blood pressure. They had been on the diabetes medications for between one month and 16 months. Three people developed symptoms within one to three months after the dose of their diabetes drug had been increased. 

The FDA and GlaxoSmithKline said on January 5, 2006 that patients who have taken Avandia reported blurry vision and swelling of the feet and legs. More than 6 million people worldwide have been prescribed Avandia. GlaxoSmithKline stated they received very rare reports of new or worsening diabetic macular edema in diabetic patients who took Avandia. The swelling of the retina can cause blurry or distorted vision. Additionally, most of those patients also reported peripheral edema, or swelling of the legs, ankles and feet, according to a letter GlaxoSmithKline sent during December 2005 to doctors. In some situations, stopping treatment or reducing the dose eliminated or improved the condition, the letter added.

If you or a loved one took Avandia and suffered a heart attack - call us toll free at 1-800-862-1260.