FDA and Drug Litigation |
Article: Study Shows Rapamune May Increase Risk Of Death In Liver Transplant PatientsA new study released by Wyeth about its anti-organ transplant rejection drug, Rapamune, says that the drug may increase the risk of death when used after a liver transplant. The U.S. Food & Drug Administration (FDA) has issued a warning to doctors about the study's results.
What is Rapamune? Rapamune is an anti-organ transplant rejection drug manufactured by Wyeth Laboratories which has been approved by the FDA for for the management of hemolytic-uremic syndrome (HUS) following kidney transplantation. However, doctors routinely prescribe it off-label to those who have undergone liver transplants – although it already contains a “black box” warning which advises doctors not to use it after liver transplants. Details of the Wyeth study Wyeth's study revealed that patients who use Rapamune (sirolimus), an immunosuppressant used to prevent the body from rejecting an organ after transplant, had a greater chance of liver rejection and a possible increased risk of death among liver transplant patients who were using a calcineurin inhibitor (CNI)-based immunosuppressive treatment and then switched to Rapamune. The study also found that:
The study's results prompted the FDA to send a warning letter to doctors on June 11, 2009 about the new findings, but the Administration says that it will investigate further to determine whether other actions are necessary. Unfortunately, liver patients aren't the only ones at risk. Risk of diabetes increased in kidney patients A study published in the Journal of the American Society of Nephrology in July of 2008 found that kidney transplant patients who used Rapamune as directed had a 36% higher chance of contracting diabetes. If you've been injured by Rapamune, consult with an experienced products liability attorney to discuss your situation and evaluate your options. Articles & Information:Proposed FDA Warning Requirements Not Consumer Friendly Study Finds Drug Makers Not Reporting All Trial Results Consumer Group Claims Botox Injections Linked To 16 Deaths FDA Gets More Money – But Will It Really Help Consumers? View all articles |