Digoxin Recall Info
Digitek Recall & Lawsuit Information - Digoxin Side Effects
Digoxin Overdose & Recall, Digitek Lawsuit & Side Effects Information
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Information about the Digoxin Toxicity Recall and Lawsuit
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An Experienced Attorney Can Help

Drugmaker Actavis Totowa issued a Digitek recall on April 25, 2008 because some tablets of the heart drug were improperly manufactured at twice the normal dose. As a result, some patients have suffered serious and potentially fatal Digitek side effects, including heart attack, stroke or other symptoms of digoxin toxicity.

Since the digoxin recall attorneys have already filed lawsuits on behalf of dozens of these patients over the Digitek side effects and injuries they suffered. These Digitek lawsuits have alleged that the heart drug was defectively manufactured because of violations of "Good Manufacturing Practices" at the plant where Digitek was produced.

If you were injured as a result of a Digitek overdose and are considering filing a lawsuit, contacting a lawyer is the first step in receiving compensation for your injuries.

An experienced pharmaceutical attorney understands the complexities of filing a Digitek lawsuit and can give you the advice you need to go forward with your case.

If you were injured after using Digitek attorneys can also assist you in the process of gathering the necessary medical information needed to prove your case.

To speak with an experienced pharmaceutical attorney about your case, contact the law office of Hissey Kientz by calling toll-free at (866) 275-4454, or by filling out a free case evaluation form to the right of this page.
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