Pradaxa Lawyers Meeting To Review Litigation Over Bleeding Problems

Lawyers representing individuals throughout the United States who are pursuing a Pradaxa lawsuit, after experiencing severe bleeding problems allegedly caused by the newer anticoagulant, will be meeting on Wednesday in Baltimore to discuss the developing litigation.

The American Association for Justice (AAJ) is holding a member’s seminar for Pradaxa lawyers representing plaintiffs-only, which will take take place at the Baltimore Sheraton Inner Harbor Hotel on April 11, 2012.

The seminar is designed to help lawyers representing plaintiffs and those who are considering taking cases. Information will be shared about Boehringer Ingelheim, the manufacturer of the drug, and presenters will explain the science behind the side effects of Pradaxa, which have been linked to an increased risk of serious and potentially fatal hemorrhages and other complications.

Did You Know?

Ticketmaster Data Breach Impacts Millions of Customers

A massive Ticketmaster data breach exposed the names, addresses, phone numbers, credit card numbers and other personal information of more than 560 million customers, which have now been released on the dark web. Lawsuits are being pursued to obtain financial compensation.

Pradaxa (dabigatran) was just introduced by Boehringer Ingelheim in the United States in October 2010, and it has already been linked to hundreds of deaths, mostly from bleeding events.

Concerns over deaths linked to Pradaxa have sparked safety investigations in the U.S., Europe and Canada, as well as a number of lawsuits over Pradaxa filed on behalf of individuals who allegely experienced problems on the medication.

Although Pradaxa was promoted as a superior alternative to Coumadin (warfarin) for prevention of strokes among individuals with atrial fibrillations, complaints allege that Boehringer Ingelheim failed to adequately warn that there is no reversal agent for Pradaxa, which may increase the consequences of bleeding that can occur while on the drug.

Pradaxa was the first approved anticoagulant from a new class of medications, known as “direct thrombin inhibitors,” which inhibit the enzyme in the blood that causes blood to clot. The medications have quickly grown in popularity, because they are easier to use than Coumadin, which requires more frequent monitoring. However, while users of Coumadin who suffer internal bleeding can be treated with Vitamin K to counter the blood thinning effects, Pradaxa and the other newer blood thinners in the same class do not have a quick fix.

The first federal Pradaxa bleeding lawsuit was filed last month, and dozens of additional claims have been brought in courts throughout the United States since then. In addition, the litigation is expected to continue to grow as Pradaxa lawyers continue to evaluate and file claims on behalf of individuals who experienced bleeding problems.

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

Ozempic MDL Court To Evaluate Need for Gastroparesis Diagnostic Testing in GLP-1 Lawsuits
Ozempic MDL Court To Evaluate Need for Gastroparesis Diagnostic Testing in GLP-1 Lawsuits (Posted 2 days ago)

A federal judge has agreed to divide lawsuits over gastroparesis injuries linked to drugs like Ozempic and Mounjaro into multiple phases, examining how the condition is diagnosed and whether plaintiffs' claims are preempted by federal laws.

Adult Woman Files Similac Lawsuit Over NEC Injuries Experienced as a Newborn
Adult Woman Files Similac Lawsuit Over NEC Injuries Experienced as a Newborn (Posted 3 days ago)

Lawsuit alleges that Abbott Laboratories failed to provide families and the medical community with adequate warnings about the risks associated with it’s cow’s milk-based Similac formula, which a now adult woman indicates has left her with life-long NEC injuries.

Amended Lawsuit Over BioZorb Implant Side Effects Outlines Problems Caused By Tissue Marker Design Defects
Amended Lawsuit Over BioZorb Implant Side Effects Outlines Problems Caused By Tissue Marker Design Defects (Posted 4 days ago)

Six breast cancer patients have asked a federal judge for permission to amend a complaint filed in March 2024, which describes problems linked to the device and painful side effects experienced when the tissue marker migrated out of position or shattered inside their bodies.