
THE LAW FIRM OF ALLEN L. ROTHENBERG

RECALL ALERT

We can help. If you or a loved one have suffered from the side effects of Digitek® Digoxin please fill out the form on this page or call 1-800-624-8888.

FDA Issues Safety Alert on Digitek Digoxin
The products are distributed by Mylan Pharmaceuticals Inc., under a “Bertek” label and by UDL Laboratories, Inc. under a “UDL” label.
The product is being recalled due to the possibility that tablets with double the appropriate thickness may contain twice the approved level of active ingredient.
The existence of double strength tablets poses a risk of digitalis toxicity in patents with renal failure. With double the prescribed amount of digoxin, the active ingredient in Digitek can cause a risk of digitalis toxicity in patients being treated for renal (kidney) failure. This Digitek overdosage can be fatal. Those Digitek users suffering from renal failure are at risk of Digitek digitalis toxtcity because they cannot excrete digitalis from their bodies like healthy people.
Symptoms of Digitalis Toxicity include: Nausea, Confusion, Seizures, Vomiting, Hallucinations, Vision problems, Dizziness, Low blood pressure, Irregular heartbeats, Abnormally fast heartbeats & Slow heartbeat and Death. Several reports of illnesses and injuries have been reported. |
Dangerous effects of Digitek® Digoxin may include: |
| Vomiting |
Cardiac Instability |
| Dizziness |
Hallucinations |
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Low Blood Pressure
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If you or a loved one has taken Digitek® Digoxin and developed any of the dangerous related issues
listed above, please
contact an expert injury attorney at
The Law Firm of Allen L. Rothenberg
1-800-624-8888 or 1-800-ROTHENBERG
for a free consultation or submit a free online case evaluation.
The case evaluation is free, and remember, we charge no fee unless we get you money. |
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