• Digitek
• Digitek Attorneys
• Digitek Arrhythmia
• Digitek Bradycardia
• Digitek Death
• Digitek Digoxin Tablets
• Digoxin Recall
• Digitek Injury
• Digitek Kidney Failure
• Digitek Medication
• Digitek Toxicity
• Digitek Lanoxin
• Digitek Overdose
• Digitek Recall
• Digitek Side Effects
• Digitek Alternatives
• Digitek Lawsuits
• Digitek MDL Lawsuit
• Digitek Litigation
• Digitek Class Action
• Digitek Lawyer

Find a Lawyer in Your State

Digitek, a medication prescribed in the treatment of arrhythmias, has been causing some patients to develop worsening heart conditions and other health problems due to the fact that some of these tablets contain two times the safe levels of the drug's active ingredient, digitalis. This news became public in April 2008 when Actavis Totowa, Digitek's manufacturer, publicly announced that it had been producing double-dosed Digitek for an unknown period of time.

With these double-dosed Digitek pills widely used across the nation, many have been consuming them and have, as a result, developed Digitek toxicity (the medical term for digitalis overdoses).

Symptoms of Digitek Injury

Depending on patients' ages, heart conditions and general health, they can experience any combination of the following symptoms of Digitek injury and/or toxicity:

• arrhythmias, particularly bradycardia (an abnormally slow heart rate that is less than 60 beats per minute)
• dizziness
• hypotension (abnormally low blood pressure)
• faintness
• kidney failure
• nausea
• vomiting

If patients continue taking this double-dosed medication and toxicity persists, Digitek injury can lead to death. Although there is no absolute way to determine how many double-dosed Digitek tablets reached patients, experts estimate that as many as half of all Digitek pills distributed were the harmful double-dosed drug.

Risk of Digitek Injury Prompts Recall

Immediately after Actavis Totowa's announcement of Digitek's defects, the Food and Drug Administration (FDA) issued a Class I recall of the medication on April 25, 2008. Class I recalls are the most imperative warnings the FDA releases and they are reserved for products or medications that have a high potential of causing serious injury and/or death.

While this recall has prevented some Digitek injury and death, for some patients, injury has already occurred and the impact is irreversible. If you or someone you love has suffered a Digitek injury, learn more about your legal options by consulting with an attorney. You may be entitled to money to help pay your medical expenses and other losses. Contact our digitek lawyer today for a free case evaluation.