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Digitek Recall - Digoxin Toxicity
The FDA has accounced a Class I nationwide recall Digitek (digoxin tablets) recall due to defects and inconsistencies in the drugs production. It is alleged that Actavis Totowa LLC produced pills that contained double the normal dosage of the prescription. Digitek is used to treat heart related illnesses and problems such as failure or arrhythmia. The systematic overdosage of this drug can lead to a complication referred to as Digitalis toxicity. Digitalis toxicity can lead to cardiac problems such as heart attack, stroke, and arrhythmia as well as kidney failure, nausea, vomiting, and dizziness and death.
The Food & Drug Administration has received many cases already of confirmed digitalis toxicity in individuals taking Digitek prescriptions. More than a dozen cases have already required hospitalization and medical attention.
If you or someone you love has been injured as a result of taking this medication, please use the form below to contact an attorney. You may also contact Attorney Justin Cook directly at 617-227-7000.
Attorney Justin Cook
Sheff Law Offices 7th Floor Ten Tremont Street Boston, MA 02108 617-227-7000 x15
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