MILLIONS IN CORPORATE PROFITS MADE BY RISKING CONSUMER SAFETY
Why Belviq® Is Off Store Shelves
First approved by the FDA in 2012, Belviq® was sold as a prescription weight loss drug that helped give users the feeling of being "full". However, a 5-year study that examined 12,000 patients found that Belviq® and its long-acting form, Belviq® XR, may lead to an increased risk of developing certain cancers.
The FDA soon announced that Belviq's® manufacturer, Eisai Inc.®, has agreed to withdraw Belviq® and Belviq® XR from the marketplace. Now, many consumers allege that Belviq's® manufacturer knew of the dangers behind their drug, but failed to warn the public or health officials.
THE FDA ISSUES A BELVIQ® RECALL DUE TO CANCER RISK –
FDA STATEMENT RELEASED STATING INCREASED CANCER RISK –
CLINICAL FOLLOW-UP STUDIES ON BELVIQ® BEGIN –
BELVIQ® BECOMES FDA APPROVED –
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