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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 FoundHarmed by Digitek medicine? Free lawsuit review of your potential case
Caraco Digoxin Recall
Lots of Digoxin (Digitek) tablets recalled by Caraco PharmaceuticalsInjured by Digoxin (Digitek) made by Caraco? Get a FREE lawsuit review
Digitek Recall
FDA: Digitek Recall Due to Some Double Doses--Free Lawsuit ReviewSearching for lawsuit information on Digitek recall? Digitek Lawyers
