Many patients assume that the maker of Pradaxa, the powerful blood-thinner that has been prescribed to thousands of patients, is only responsible for the production of the drug that caused their internal bleeding. This isn’t necessarily the case. In many defective drug or defective medical product lawsuits, the maker is not only legally responsible for the way a product was made, but also how it was designed and marketed.
If you’re like the thousands of Americans who have reported Pradaxa adverse events to the U.S. Food and Drug Administration (FDA), you may want to carefully explore the full scope of Pradaxa liability. By asking questions about design and marketing as well as production, you may find important answers to your case – and to the liability associated with your injury.
Want to learn more about your rights under the law? The attorneys at the Dallas law firm of Fears Nachawati have years of experience helping defective drug victims like you. Get started with your recovery by talking to us today. For your free consultation, call us at 1.866.545.8364 or email mn@fnlawfirm.com. We’re ready to help you.