Friday, July 10, 2009

Defects Leads to Heart Medication Digitek Recall

Did you or a loved one use Digitek?

A great number of patients who were prescribed the heart medicine Digitek have suffered significant and probably lethal complications as a consequence of producing defects with the drug. As a consequence of these Digitek complications cases, the drug's manufacturer issued a national Digitek recall on April 25, 2008.

Digitek is a type of the heart medication digitalis; it is also known generically as digoxin. Digitek and other digoxin drugs operate by accelerating the quantity of calcium in the heart in order to strengthen the heart beat. Digitek is prescribed to treat sufferers with an irregular heartbeat or congestive heart failure.

According to a public relations release issued at the time of the recall, some pills of the drug were incorrectly made at twice their normal thickness. As a result, some patients were getting a hefty dose of the drug, which could cause significant Digitek complications as a consequence of a digoxin overdose.

In the most serious cases, patients who have experienced a digoxin overdose may suffer a cardiac arrest, stroke or, probably, death. Some of the other Digitek complications suffered by patients include low blood pressure, an unstable pulse, fainting, misunderstanding, revulsion, barfing or other symptoms.

Some patients who had a Digitek overdose have recently made contact with a attorney about filing a Digitek lawsuit. These patients have alleged that defectively manufactured Digitek tabs put patients at an elavated likelihood of a digoxin overdose and major and potentially deadly Digitek side effects.

If you or a loved one have been hurt as a consequence of a Digitek overdose, you may with to speak with a Digitek lawyer about filing a suit. You may be entitled to financial compensation for your loss and injuries.

Please visit this website to review your case for free.

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