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Produced by Actavis Totowa LLC, Digitek is a medication prescribed to those with congestive heart failure and/or arrhythmias. While proper amounts of Digitek medication can improve heart function and blood flow for some, excess amounts of digitalis, the medication's active ingredient, can result in Digitek toxicity and possibly death.

Digitek Recall

Initial reports of the dangers of Digitek were first made public in April 2008 when Actavis Totowa, an Icelandic pharmaceutical manufacturer, announced that some of its Digitek pills were made with double the safe amounts of digitalis. Although Actavis Totowa's announcement triggered an immediate Class I FDA recall of this medication, many people have already suffered significant injury and/or death due to the double-dosed Digitek.

Digitek Can Cause Arrhythmia

Digitek, a medication used to treat arrhythmias, can ironically result in more severe arrhythmias if taken in excess. In fact, if double-dosed Digitek is taken for significant periods of time, patients will develop Digitek toxicity, a condition in which continual digitalis overdoses cause serious health complications.

Along with new or worsened arrhythmias, other symptoms of Digitek toxicity can include:

• dizziness or feelings of faintness
• lowered blood pressure
• nausea and/or vomiting
• renal (kidney) failure
• fatality, if Digitek toxicity remains untreated

Despite the difficulty in knowing exactly how much of the Digitek in circulation contains two times as much digitalis, experts estimate that as much as 50 percent of all Digitek tablets produced are the harmful, double-dosed version.

If you are currently taking Digitek…

See your doctor immediately if you suspect you are taking the double-dosed Digitek or if you start experiencing symptoms of Digitek toxicity. Do not abruptly stop taking Digitek, as immediate cessation can result in further health problems, particularly for those with more serious heart conditions.

With the guidance and supervision of your doctor, you can slowly decrease your dosage of Digitek and replace it with a safer substitute. Similarly, your doctor can help you pursue the best courses of treatment for any Digitek side effects you may have developed.

Digitek Arrhythmia Lawsuits

Upon the 2008 announcement of the manufacturing errors that resulted in double-dosed Digitek, the FDA mandated a Class I recall of Digitek, alerting the public of the significant dangers and risks of death associated with this medication. Although this recall successfully took large amounts of Digitek out of circulation, for some patients, the damage has already been done.

If you have suffered arrhythmia due to Digitek treatment, contact an experienced digitek lawyer today to discuss your legal options. You may be entitled to compensation for your losses.