Digitalis Toxicity Caused By Digitek Recalled Tablets

Digitek was recalled in 2008 due to the production of tablets with twice the approved amount of digoxin in them. Digoxin, the active ingredient in Digitek, is toxic when taken in large doses. The condition caused by over consumption of Digitek (digoxin) is called digitalis toxicity, and it can be fatal.

Digitalis toxicity occurs when digoxin accumulates in the body at a quick rate, and the body is unable to rid itself of the excess digoxin. Digitalis toxicity is also more likely to occur in patients who have an existing kidney disease or kidney failure, and in those taking diuretics.

Digitek is frequently prescribed to patients suffering from irregular heart beats or heart failure. Unfortunately, patients suffering from heart failure are also commonly prescribed diuretics. Diuretics typically cause potassium loss in patients, and low potassium levels increase the risk of developing digitalis toxicity.

Digitek (digoxin) recall tablets greatly increase the risk of developing digitalis toxicity. Digitalis toxicity symptoms include slowed heartbeat, vision problems, hallucinations, seizures, and many more serious symptoms. Digitalis toxicity can also result in death.

If you have taken recalled Digitek (digoxin) tablets and developed digitalis toxicity, or if you have lost a loved one due to digitalis toxicity contact McEwen Law Firm today. Our digitalis toxicity attorneys undertand the terrible side effects recalled Digitek tablets cause and are dedicated to helping provide you with legal compensation.

McEwen Law Firm provides free, no obligation, consultations. If you have any questions about the Digitek recall or would like to go forward with your case please contact us at (800) 732-3070 or use our online contact form.