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Thursday, 04 September 2008

Digitek MDL Established

The United States Judicial Panel on Multidistrict Litigation has ordered that all federal lawsuits related to defective, double strength Digitek (commonly known as Digitalis or Digoxin ) be moved to the U.S. District Court for the Southern District of West Virginia. This consolidation comes after an April 2008 recall on all lots of the prescription drug after discovery that some tablets twice as thick as normal contained double the appropriate amount of medication.

60+ Digitek Lawsuits Filed 
 
At least 60 Digitek lawsuits have been filed in federal courts across the country. Defendants include Actavis Totowa, LLC, Actavis, Inc., Actavis Elizabeth, LLC, Actavis US, Mylan, Inc., Mylan Pharmaceuticals, Inc., Mylan Laboratories, Inc., Mylan Bertek Pharmaceuticals and UDL Laboratories, Inc.
 
Seventeen of the pending federal suits have been filed in the Southern and Northern District of West Virginia. The other pending cases come from Cleveland, Ohio; New Orleans, La.; Chicago, Ill.; Philadelphia, Pa.; Ft. Myers, Fla.; and Kansas City, Mo.

Digitek Lawsuits - Contact a Lawyer

 

If you or a loved one have been seriously injured or a loved one has died as a result of this digitalis digoxin toxicity or an overdose of Digitek, please call us immediately for a Free Digitek Recall Lawsuit Evaluation at 1-800-883-9858 or learn more information on whether your case should be filed as a separate lawsuit or part of a global Digitek Class Action Lawsuit and more about the MDL formed recently as described above.

 

Nationwide Help is Available - Call us at 1-800-883-9858

 

POSTED BY: DW AT 09:33 am   |  Permalink   |  E-mail this
Digitek Digoxin Toxicity, Digitalis Toxicity Overdose Lawsuits and Digetek Recall Deaths - Digoxin / Digitalis Toxicity.


   

      

 

 

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Digoxin is used to treat congestive heart failure and atrial fibrillation, "A- Fib", atrial flutter (types of fast heartbeats). Digoxin helps the heart to beat more strongly and regularly. However double the prescribed amount of digoxin, the active ingredient in Digitec can cause a risk of digitalis toxicity in normal cardiac patients and especially in patients being treated for renal (kidney) failure. Digetek is a registered trademark of ActavisTotawa and distributed by Mylan Pharmaceuticals, Inc., with a "Bertek" label and by UDL Laboratories, Inc. with a "UDL" label. FDA digitech recall information and digetec recall news and updates. Talk to a Digitek Lawsuit Lawyer about filing a digitec recall Lawsuit or about the details of a possible digetek class action lawsuit. Free Case Evaluation

 

FDA warning Reglan may cause Tardive Dyskinesia (TD) a rare side effect of long time Reglan usage. Reglan has been linked to Tardive Dyskinesia. Tardive Dyskinesia is a disorder characterized by involuntary movements of the arms and legs as well as facial twitching, frowns twitching of the face and tongue similar to Parkinsons disease. See Metoclopramide and Tardive Dyskinesia TD for more information about reglan side effects. See Reglan Tardive Dyskinesia (TD) side effects lawsuits.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

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