Digitek Recall Lawsuit | Digitalis Digoxin Toxicity Lawyer - Actavis Standards for Quality Control

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Actavis Quality and compliance

Effective quality management is of paramount importance to Actavis' success.

Actavis has prepared a Corporate Manual that sets the standard of performance for all Actavis operations. The manual outlines Actavis' quality management system and environmental, health and safety (EHS) management system.

The implementation of an effective quality management system at each site according to the requirements in the Corporate Manual is supported by the Actavis Quality & Compliance team. The status and performance at each site is then closely monitored by the Actavis Quality Board.

Actavis has manufacturing operations in numerous different countries with diverse regulatory requirements. In order to ensure local compliance our manufacturing sites are all regularly assessed internally and inspected by authorities. Quality audits are undertaken as well, initiated by existing and potential customers.

STANDARDS & COMPLIANCE TO EXCELLENCE IN ACTAVIS' OWN WORDS

POSTED BY: dw AT 10:52 am | Permalink | E-mail this

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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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