Xarelto Lawsuit Ends In $27.8M Verdict Over Gastrointestinal Bleeding Injury

A Philadelphia jury has ordered Bayer and Johnson & Johnson to pay $28 million to a woman who suffered severe gastrointestinal bleeding due to the side effects of Xarelto, a controversial anticoagulant that is the subject of nearly 20,000 other cases that raise similar claims that the drug makers failed to adequately warn consumers and the medical community about the bleeding risks. 

Xarelto (rivaroxoaban) was introduced in 2011, as the second member of a new class of drugs known as novel oral anticoagulants. The drugs were were marketed as easier to use than warfarin, which had been the go-to anti-clotting treatment for decades. However, as an alarming number of adverse event reports involving severe and often fatal bleeding problems began to emerge, a mounting number of Xarelto lawsuits began to be filed against the drugs manufacturers.

The trial was the first to take place in Pennsylvania state court, where about 1,500 claims have been filed. However, more than 18,000 more Xarelto cases are pending in the federal court system, where centralized pretrial proceedings have been established.

Did You Know?

AT&T Data Breach Impacts Millions of Customers

More than 73 million customers of AT&T may have had their names, addresses, phone numbers, Social Security numbers and other information released on the dark web due to a massive AT&T data breach. Lawsuits are being pursued to obtain financial compensation.

Learn More

Each of the claims raise similar allegations involving uncontrollable gastrointestinal bleeding, brain bleeds or other injuries that occurred after doctors were unable to stop hemorrhaging among users of Xarelto. Plaintiffs claim that the drug makers provided false and misleading information for consumers and the medical community, failing to adequately warn about the risks associated with their medication.

The jury awarded Lynn Hartmann $1.8 million in compensatory damages, but added an additional $26 million in punitive damages designed to punish the companies for recklessly disregarding the health and safety of patients.

The verdict is the first victory for plaintiffs, after three prior federal trials resulting in defense verdicts. However, additional bellwether trials are expected to help the parties gauge how different juries may respond to certain evidence and testimony that is likely to be repeated throughout the litigation.

While the outcomes of these early bellwether trials are not binding on other plaintiffs with claims bending, they are closely watched by the parties, and may influence Xarelto settlements, which would be necessary to avoid the need for thousands of individual trials nationwide.

0 Comments

Share Your Comments

I authorize the above comments be posted on this page*

Want your comments reviewed by a lawyer?

To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.

NOTE: Providing information for review by an attorney does not form an attorney-client relationship.

This field is for validation purposes and should be left unchanged.

More Top Stories

Novo Nordisk Fails To Warn About Risk of Gastroparesis from Wegovy, Lawsuit Alleges
Novo Nordisk Fails To Warn About Risk of Gastroparesis from Wegovy, Lawsuit Alleges (Posted 2 days ago)

A Wegovy gastroparesis lawsuit filed by a Pennsylvania couple accuses the manufacturer, Novo Nordisk, of failing to provide adequate warnings about the true risks of the injectable weight loss drug.

Lawyers
Lawyers "Optimistic" Suboxone Tolling Agreement Will Be Reached For Tooth Decay Lawsuits (Posted 3 days ago)

Plaintiffs and defendants involved in Suboxone tooth decay lawsuits say they are close to a deal that would allow the filing of federal complaints after some state statue of limitation laws would have disqualified plaintiffs from filing.

Lawsuit Indicates Tepezza Hearing Impairment Warnings Were Delayed By Horizon Therapeutics, Disregarding Safety of Users
Lawsuit Indicates Tepezza Hearing Impairment Warnings Were Delayed By Horizon Therapeutics, Disregarding Safety of Users (Posted 4 days ago)

New Jersey man indicates he has been left with permanent hearing impairment from Tepezza, alleging that Horizon Therapeutics failed to instruct doctors about the importance of conducting hearing tests on patients using the thyroid eye disease drug.