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Xarelto Lawsuit: Philadelphia Court orders for mass tort docket

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A Xarelto lawsuit multi-district litigation (MDL) has been set up in Pennsylvania following a January 21, 2015 Order of the Philadelphia Court of Common Pleas. At least 75 litigations are filed in the state claiming irreversible bleeding and fatal side effects linked to ingestion of the blood thinner. The establishment of the mass tort means all present and future claims submitted by a Xarelto attorney in the state will be centralized for consolidated pre-trial proceedings at the court of Judge Kevin Dougherty.

Janssen and Bayer Healthcare are named as defendants in over two-dozen Xarelto bleeding side effect litigations. The numbers of lawsuits are expected to amplify significantly considering the fact that the FDA received reports of over 200 deaths and about 700 bleeding injuries associated with the blood thinner between January and May 2013. Actual figures (unreported) may run into thousands. The 2012 figures, 151 died and 2,081 hospitalized, led the Institute for Safe Medication Practices to name Xarelto as one of the “10 most frequently named” drugs for side effects.

Our firm has filed a Xarelto related lawsuit in Tennessee Federal Court.

Xarleto Lawsuit Blames Manufacturer

A recent Xarelto lawsuit filed in a West Virginia federal court alleges that the manufacturers ignored research reports highlighting greater “risk of gastrointestinal bleeding and even the need for blood transfusion to eliminate irreversible side effects” associated with the blood thinner and marketed the drug despite potential threats to users.

The plaintiff, a woman, was prescribed the drug after she was diagnosed with atrial fibrillation. She had gastrointestinal bleed that did not stop with any antidote and ultimately she required blood transfusion to prevent fatal conditions. According to the Xarleto attorney representing her, “the Institute for Safe Medication Practices noted that, even during the approval process, ‘FDA (reviewers) also questioned the convenient once-a-day dosing scheme … (saying) blood level studies had shown peaks and troughs that could be eliminated by twice-a-day dosing…’ and in the event of hemorrhagic complications there is no available reversal agent.”

The Xarleto product liability lawsuit seeks damages based on “negligence, fraudulent misrepresentation, fraudulent concealment, negligent misrepresentation, fraud and deceit, violation of the West Virginia Consumer Credit & Protection Act and loss of consortium.”

Study Rejects Xarleto Superiority Over Warfarin

A Japanese study reported in the Journal of Cardiology has negated the manufacturer claim that using Xarelto does not require blood monitoring, which is an essential requirement for those on Warfarin. Researchers examined 136 patients administered the blood thinner under observation and discovered that “, the drug caused a prolonged “thinning” effect, making them more likely to experience serious bleeding events” within two weeks. They advised for blood monitoring as in the case of Warfarin to prevent the bleeding risk caused by prolonged “thinning” effect from leading to fatal hemorrhage in patients and hospitalization of users.

Xarelto Bleeding Side Effect

  • Death due to irreversible internal bleeding
  • Gastrointestinal hemorrhage
  • Stomach bleeding
  • Stroke due to hemorrhage
  • Adrenal hemorrhage
  • Cerebral hemorrhage
  • Intracranial hematoma in brain

Xarelto blood thinner was approved in 2011. Despite carrying a significant internal bleeding risk, the manufacturers promoted the drug as a next-generation anticoagulant with significant benefit over Warfarin, another blood thinner extensively used for decades. While positive results were advertised, the drug makers kept negative clinical findings away from public domain, which has been cited in most Xarleto lawsuits. Again, Bayer and Janssen introduced it and engaged in aggressive marketing efforts without suggesting any effective antidote to reverse serious bleeding effects, if happens.

If you have a potential Xarelto lawsuit related to the blood thinner side effects, please contact us or call on 1-800-632-1404 for a free consultation with our experienced Xarelto attorney.

Contact a Xarelto Injury Lawyer Today.

If you or a loved one was injured or died after ingesting Xarelto, please contact us immediately.

For a Free Case Evaluation:

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    NOTE: Our team of attorneys will review potential cases for all fifty states, including Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin and Wyoming.

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    Xarelto Lawsuit: Plaintiffs Allege Life-Threatening Bleeding Linked to Blood Thinner

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    FREE CASE EVALUATION: 1-800-632-1404

    A Xarelto lawsuit filed by an 87-year-old man claims that he experienced life-threatening internal bleeding caused by the blood thinner. The litigation filed in a California northern district federal court in October 2014 cites gastrointestinal hemorrhage as one of the blood thinner side effects. The plaintiff was treated with the anticoagulant drug for some months until October 2014, when he suffered from uncontrolled hemorrhage in the absence of any antidote to the drug, the Xarelto attorney representing the man claims.

    The litigation followed a similar Xarelto internal bleeding lawsuit filed by a California woman in August 2014. Shirley Boynton began using the blood thinner in April 2012. She had life-threatening bleeding within six months that resulted in debilitating and permanent injuries. Had she been aware of such potential side effects or read about hemorrhaging risk on its label, the plaintiff would have avoided it, according to her Xarelto lawsuit filed in a New York district court.

    The two lawsuits have named Bayer and Johnson and Johnson as defendants and seek $10 million in damages.

    Xarelto Lawsuit: Blood Thinner Side Effects Research

    The FDA approved Bayer’s oral anticoagulant Xarelto, which contains rivaroxaban, in July 2011. Marketed by Janssen, the drug is prescribed to people with knee surgery or others at the higher risk of blood clotting. It inhibits factor Xa, which in turn “interrupts the intrinsic and extrinsic pathway of the blood coagulation cascade.” In November 2011, the drug was allowed to treat patients suffering from atrial fibrillation or clots in blood arteries, a possible indication of stroke.

    However, researchers have questioned the efficacy of the drug advertised by the manufacturers. Though the impact is slated to last 8 to 12 hours, the anticougaltion properties in the body continue to remain subdued for 24 hours. The absence of any readily available antidote makes the Xarelto blood thinner even more dangerous and may lead to excessive, life-threatening bleeding, as cited by many product liability lawsuits.

    According to the American Heart Association, Xarelto is likely to cause the three-time higher risk of internal bleeding acute ill patients. The risk is four-time more in those with preexisting Acute Coronary Syndrome, asserts one of its reports presented in November 2013.

    The German newsmagazine Der Spiegel carried a report in 2013 that linked Xarelto blood thinner to 72 deaths and 896 hemorrhage events between January and October 2013. The figures for 2012 were 58 deaths and 692 internal bleeding complaints.

    A comparative study by Johnson & Johnson conducted in April 2011 discovered that patients treated with oral anticoagulant Xarelto for more than 35 days twice more prone to developing bleeding adverse events compared to Lovenox, an injectable blood thinner with enoxaparin as the main ingredient.

    The ROCKET AF clinical trial results reported the Journal of the American College of Cardiology in December 2013 also demonstrated bleeding or hemorrhage as the most common Xarelto side effect. Funded by the manufacturers, the study covered 14,000 patients treated with Xarelto and Warfarin blood thinners over a two-year period. While both drugs were found to cause identical side effects, Xarelto was not superior to Warfarin, the researchers concluded.

    It was also discovered that Xarelto-induced hemorrhage has less impact in the brain, but had significant bleeding rate for stomach and intestine.

    Xarelto Blood Thinner Side Effects

    • Cerebral hemorrhage
    • Gastrointestinal bleeding
    • Stroke
    • Wrongful death
    • Stomach and adrenal bleeding
    • Subarachnoid, subdural, and extradural hemorrhages
    • Swelling leads to intracranial hematoma in brain

    Xarelto Lawsuit

    A motion was filed early October 2014 to centralize all Xarelto hemorrhage lawsuits filed in different states. At that time about two dozen such litigations citing bleeding injuries were pending at the federal judicial system spread over 10 states. The plaintiffs have sought MDL pretrial consolidation at the Southern District Court of Illinois presided by David R. Herndon. The U.S. JPML planned to meet in Charleston, SC, on December 4 or in Miami, FL, on January 29 is expected to take a look at consolidation.

    Meanwhile, there has been a noticeable increase in the filing of Xarelto lawsuits claiming wrongful death, fatal and non-fatal internal bleeding, coma, cerebral hemorrhage, and other types of injuries. The actual litigation numbers may run in hundreds as many affected individuals contacting Xarelto lawyers to examine the product liability claims.

    For a free consultation with our experienced Xarelto attorneys, please contact us or call on 1-800-632-1404.

    Contact a Xarelto Injury Lawyer Today.

    If you or a loved one was injured or died after ingesting Xarelto, please contact us immediately.

    For a Free Case Evaluation:

    TOLL FREE: 1-800-632-1404

    EMAIL: click here

    FILL OUT THIS FORM:

      Your Name (required)

      Your Email (required)

      Your Telephone Number

      What year was your child born?

      Where do you live (state)?

      NOTE: Our team of attorneys will review potential cases for all fifty states, including Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin and Wyoming.