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| Have You Been Harmed by Digitek? |
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Digitek / Digoxin Recalled by FDA On April 25, 2008 the FDA in conjunction with Actavis Totowa LLC issued a Class I recall for the heart medication Digitek (Digoxin)because some tablets have been found to contain twice the recommended amount of the active ingredient. The tablets were distributed in the US by Mylan Pharmaceuticals Inc, under a “Bertek" label, and also by UDL Laboratories Inc, under “UDL” a label.Several injuries and illnesses associated with this recall have been reported to the FDA.An overdose of the medication can cause a potentially fatal condition known as digitalis toxicity. Digitalis toxicity can cause a patient’s blood pressure to drop to dangerously low levels resulting in death. Digitalis toxicity can also be associated with dizziness, nausea, vomiting, cardiac instability, hallucinations, and seizures.If you or a loved one has taken Digitek (Digoxin) and has experienced these symptoms you may have a claim. Contact Reich and Binstock today by filling out the form on this page or call us toll free at 1-800-622-7271. |
