Digitek (digoxin tablets) Recalled Due to Potentially Deadly Manufacturing Defect

Digitalis

Digitalis Toxicity

All lots of Digitek have been recalled because it is suspected that they contain twice the amount of the approved level of active ingredient. The double strength pills may lead to digitalis toxicity in patients experiencing renal failure or in those patients with decreased tolerance to the drug.

Kidney patients may experience nausea, vomiting, dizziness, low blood pressure, and serious heart problems including cardiac instability and bradycardia (slow heart rate). Digitalis toxicity can occur when a patient continues to take too much of the drug over a period of time or from one overdose.

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