The Food and Drug Administration has given a whistle-blower scientist permission to publish data indicating that as many as 139,000 people had heart attacks that may be linked to Vioxx, the scientist’s lawyer said Monday.
Dr. David Graham, who works in the FDA’s office of drug safety, has said he was not allowed to publish his data questioning the safety of Vioxx, a pain medication principally used to treat osteoarthritis. Additionally, an FDA official sent e-mail messages to the medical journal Lancet trying to persuade the journal not to publish the data.
Citing its own safety concerns, manufacturer Merck & Co. voluntarily pulled Vioxx from the market in late September.
Graham testified in November before a Senate committee that the FDA fumbled in its handling of safety concerns about Vioxx and had mishandled concerns about five other widely used drugs. He contended that FDA has an inherent conflict of interest that triggers “denial, rejection and heat” when safety questions emerge about products it has approved. The FDA denies the allegations, and controversy over the agency’s role continues.
The report will be resubmitted to The Lancet, a British medical journal, which is expected to publish it, said Tom Devine, Graham’s attorney.