Lawyers for Digitek / Digoxin Patients

Digitek (Digoxin) tablets are being recalled because they may contain a dangerous double dose of their active ingredient. Digitek is distributed by Mylan Pharmaceuticals and sold under the labels "Bertek" or "UDL." If you or someone you love were injured by Digitek or Digoxin, please contact our Digitek lawyers for a free consultation. Call 1-866-468-8631 or click here to contact us online.

Digitek (Digoxin), also known as Cardoxin, Lanoxicaps or Lanoxin, was recalled in a nationwide recall announced in April 2008. Actavis Totowa LLC (formerly known as Amide Pharmaceutical, Inc.), manufactures Digitek for distributors Mylan Pharmaceuticals Inc. and UDL Laboratories.

Digitek Overdose

Digitek (digoxin) is prescribed to treat heart failure and irregular heartbeat (arrhythmia). If you took Digitek, Cardoxin, Lanoxin or Lanoxicaps and suffered from overdose, it may be due to taking tablets that contained twice the active ingredient as approved. Symptoms of a digoxin overdose include any of the following:

• Nausea
• Vomiting
• Decreased appetite
• Diarrhea
• Confusion
• Seizures
• Hallucinations
• Fatigue
• Irregular heartbeats
  

SimmonsCooper has represented thousands of pharmaceutical clients and recovered more than $100 million in verdicts and settlements.*  We have experience in litigating complex medical matters. We have taken a leadership role in standing up for individuals who have been injured by dangerous or defective drugs.

If you or someone you love were injured by Digitek, please contact our Digitek lawyers for a free consultation. Call 1-866-468-8631 or click here to contact us online.

^{* Please note that recovery results vary per client. The recovery amounts in each case reflect the specific facts of that case. Further, recovery amounts in past cases are not a guarantee of future results.}
 

Representative Matters

Resources for Clients

Digitek Tablets Recalled

Digitek FDA Warning