By Steve Levine
This page describes a drug recall and the related lawsuits. The statements below are unproven allegations. No manufacturer has been found liable, there is no certified class or approved settlement, and the litigation has largely wound down. This page is informational and is not legal or medical advice.
In February 2020, the FDA requested the withdrawal of Belviq and Belviq XR (lorcaserin) from the U.S. market after a five-year safety trial of about 12,000 patients found that more people taking lorcaserin were diagnosed with cancer than those on placebo. The FDA reported a range of cancer types, including pancreatic, colorectal, and lung cancer.
Generally, adults who took Belviq, Belviq XR, or another brand of lorcaserin and were later diagnosed with cancer, or families of those who died, may have had a claim. Eligibility always depended on the diagnosis, the exposure history, and the facts of each case.
In 2021, the Judicial Panel on Multidistrict Litigation declined to consolidate Belviq cases into a federal MDL, so claims have proceeded as individual cases in state and federal courts. As of 2026, the litigation has largely wound down and many firms are no longer accepting new Belviq cases. State statutes of limitations may now bar many new claims.
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