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On March 12, 2010, the U.S. Food and Drug Administration (FDA) announced a boxed warning that patients whose livers do not process Plavix may not receive the full benefits of the drug. As a result, for some patients Plavix has less of an ability to prevent heart related issues and stroke. According to Fox News on the very same day, a boxed warning is “the FDA’s most severe warning”. The FDA places this warning on drugs that may lead to death or serious injury.
If you or a loved one have suffered from heart problems, stroke, or excessive bleeding and have been using Plavix you may be entitled to compensation.
Plavix® is a registered trademark of Bristol-Myers Squibb and Sanofi-Aventis.
Note - Do not change medications without first consulting your doctor.
