Institute of Safe Medication Practices Report
According to an industry consumer watchdog, the Institute of Safe Medication Practices (ISMP), noted that the number of serious adverse events with Xarelto bleeding side-effects is significant and worse that for another new blood thinner, Pradaxa. Xarelto prescriptions increased to nearly 1 million prescriptions per quarter, according to ISMP. ISMP monitors and analyzes serious adverse drug events reported to the U.S. Food & Drug Administration (FDA).
Xarelto Increasd Adverse Reports
As the usage of Xarelto increases in the United States, many Xarelto uncontrollable bleeding lawsuits are being filed against Bayer AG, and Johnson and Johnson, the manufacturers and distributors of Xarelto. In the first quarter of 2013, ISMP found 680 serious adverse event reports associated with Xarelto, compared to 528 complaints for Pradaxa. According to ISMP the trend is mostly due to doctors changing prescriptions for their patients from Pradaxa to Xarelto.
Xarelto and Pradaxa: No Antidote
Warfarin, the traditional go to blodd thinner drug, was approved by the FDA in 1954 and marketed under the brand names of Coumadin. There is no approved antidote for oral anticoagulants, such as Xarelto and Pradaxa. If significant bleeding should occur in patients taking the blood thinners then this lack of an antidote means that patients who suffer seemingly minor injuries are at risk of uncontrolled bleeding that could be fatal.
Xarelto History
Xarelto is a Bayer drug that is marketed in the US by Johnson & Johnson and its subsidiary, Janssen Ortho LLC. Xarelto was initially approved by the FDA in July 2011 to reduce deep vein thrombosis and pulmonary embolism in patients who had knee or hip replacement surgery (preventive use). Xarelto use was expanded in November 2011 to reduce stroke and blood clot risks in patients with atrial fibrillation. Xarelto received FDA approval again in November 2013 to treat deep vein thrombosis and pulmonary embolism.
Xarelto Lawsuits
Hundreds of adverse event reports have been submitted to the FDA suggesting a link between Xarelto and bleeding injuries or death. Similar allegations have been raised in lawsuits, that the drug makers failed to adequately warn about the bleeding risk or lack of an effective Xarelto reversal agent. Xarelto was heavily marketed as superior to warfarin because it is easier to take and require no monitoring to maintain the correct dosage.
One Comment
Glenn Sedgwick
I chatted with a person in your firm. I now see the drug E er also was not in use till 2011. My aneurysm was in 2007, so disregard.
Glenn Sedgwick
Comments for this article are closed.