Xarelto’s most serious complication is uncontrollable internal bleeding, a life threatening injury. Xarelto has also been reported to cause the following injuries:
If you or a loved one were injured or died due to any of the above complications you may qualify for legal representation.
Pharmaceutical giants Bayer Healthcare and Johnson & Johnson are facing multiple lawsuits for wrongful deaths and Internal Bleeding Injuries related to Xarelto®. A growing number of victims and families have pursued justice by finding legal representation willing to take on these pharmaceutical giants .
Drug manufacturers can be held accountable for any injuries caused by undisclosed but known risks associated with the use of the medication. When a family member is injured or dies because of adverse side effects associated with Xarelto®, the drug companies might be liable for damages including medical bills, lost earnings, pain and suffering prior to death and other forms of compensation.
It is Free to have your Case reviewed by an attorney the process is simple either contact us or call (888) 508-0836. You may be entitled to Financial Compensation for your pain and suffering.
Free Case Review The FDA (Food and Drug Administration) has received numerous complaints regarding individuals suffering uncontrollable internal bleeding after taking Xarelto®. In 2013 the FDA formally issued a warning to Johnson and Johnson regarding the misleading advertisements they marketed to the public. In this warning the FDA clearly states that their Ads where false or misleading because it minimized the risks associated with Xarelto®.
Xarleto was manufactured by Bayer and marketed by Janssen Pharmaceuticals a Johnson and Johnson company. 
The FDA originally approved Xarelto® for treatment of patients who have hip or knee replacement surgery. The role of the drug is to mitigate the risk of blood clots in patients with atrial fibrillation (AF). Later, the drug was approved for treatment of pulmonary embolism (PE) and deep vein thrombosis (DVT) based on a “fast-track regulatory review”.
In May of 2012 the FDA ultimately declined to recommend Xarelto® for expanded use citing “concerns over dangerous bleeding outweighed evidence that the drug helped reduce the risk of blood clots in patients with serious heart problems.” These lawsuits accuse the manufacturer of insufficient drug testing and negligence prior to taking Xarleto onto the market. If you or a loved one suffered from bleeding or other side effects caused by Xarelto®, may be eligible to take legal action.
Xarelto® has recently come under fire for failure to warn consumers of the drug’s potential adverse side effects, which include uncontrolled internal bleeding. In January, an FDA report disclosed 593 incidents of uncontrolled bleeding associated with the anticoagulant. Xarelto® was associated with 151 deaths as well as 2,081 serious incidents in 2012 alone. This was reported in a study released in 2013 by the Institute of Medication Practices and warns of the dangers this drug can cause.
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