Weitz & Luxenberg is no longer taking Digitek cases

Did your loved one received a defective double dosage of Digitek (generic digoxin)?

Digitek lawyer: "The public has a right to know what quality assurance measures have been in place and why tablets with double the approved dosage were being sold.”

A Class I recall was issued by Actavis Totowa LLC on April 25, 2008 for all lots of the heart drug Digitek (generic name digoxin) because some have been found to contain twice the approved levels of active ingredient than is appropriate.

Digitek is used to treat heart failure and abnormal heart rhythms. The existence of double strength tablets poses a risk of digoxin toxicity in patients with renal failure.

Digoxin toxicity can cause nausea, vomiting, dizziness, low blood pressure, cardiac instability and bradycardia. Death can also result from excessive intake of digoxin.

A number of families have already come forward to say the death of a loved one was caused by defective Digitek tablets. People who have been harmed by Digitek should complete the form below for a free legal review of their potential case.

see also:

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