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Digitek Drug

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All lots of Digitek heart drug recalled due to risk of double-strength tablets


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All lots of the heart drug Digitek (generic name digoxin) have been recalled because some have been found to contain twice the approved levels of active ingredient than is appropriate.

Unfortunately, this recall comes too late for the families whose loved ones ingested the potentially deadly dose.

According to the Food and Drug Administration, several reports of illnesses and injuries have been received.

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.

Patients taking Digitek should contact their physician immediately for medical advice.

People who have been harmed by Digitek and would like to be in touch with a Digitek lawyer may complete the form below for a free legal review. A representative of our firm will be in touch with you as soon as possible.


see also:

Digitek Medicine Lawyers: Digitek Medicine Recalled After Double-Strength Tablets Found
Harmed by Digitek medicine? Free lawsuit review of your potential case

Caraco Digoxin Recall Lots of Digoxin (Digitek) tablets recalled by Caraco Pharmaceuticals
Injured by Digoxin (Digitek) made by Caraco? Get a FREE lawsuit review

Digitek Recall FDA: Digitek Recall Due to Some Double Doses--Free Lawsuit Review
Searching for lawsuit information on Digitek recall? Digitek Lawyers

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