A class I recall is being issued on all Digitek (digoxin) tablets, which may contain twice the approved level of digoxin.The existence of double-strength pills pose a risk of digitalis toxicity, which can result in nausea, vomiting, low blood pressure, cardiac instability, bradycardia and even death.
Digitek is a registered trademark of Actavis Totowa (formerly Amide Pharmaceutical, Inc.) for their digoxin tablets, which are prescribed to treat heart failure and abnormal heart rhythms. The drug is distributed by Mylan Pharmaceuticals Inc., under a “Bertek” label and by UDL Laboratories, Inc. under a “UDL” label.
Patients taking Digitek should contact their physician immediately for medical advice. Retailers who carry Digitek should return the product to the place of purchase.
Story plus a pic of the recalled drug at
http://www.usrecallnews.com/2008/04/urgent-digitek-digoxin-recall.htmlPosted as a public service, since digoxin is a first line drug for congestive heart failure and a lot of folks here are probably on it.
If you are on this particular drug and have had problems with very slow heart rate, dizziness, nausea, or yellowish vision, please call your doctor NOW. If you can't get through, go to an ER.