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Have You Been Harmed by Digitek? |
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Digitek / Digoxin Recalled by FDA On April 25, 2008 the FDA in conjunction with Actavis Totowa LLC issued a Class I recall for the heart medication Digitek (Digoxin)because some tablets have been found to contain twice the recommended amount of the active ingredient. |
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Read more... [Have You Been Harmed by Digitek?]
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Woman’s Estate Sues Mylan Over Digitek Overdose |
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 The administrix of the estate of Elizabeth Starr has filed a lawsuit against the Pennsylvania based Mylan Pharmaceuticals. The company was responsible...
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Read more... [Woman’s Estate Sues Mylan Over Digitek Overdose]
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Digitek Maker Recalls All Drugs Made at NJ Plant |
 Earlier this month generic drug maker, Actavis Totowa, announced a voluntary recall of all medications produced at their Little Falls, New Jersey facility. |
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Read more... [Digitek Maker Recalls All Drugs Made at NJ Plant]
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Class I Recall Issued for Digitek Tablets |
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Have You Been Harmed By Trasylol? |
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 Trasylol Pulled From the Market
Recently Trasylol was pulled from the world wide market after the Canadian BART Study had to be haulted when alarmingly disproportionate numbers of patient being treated with Trasylol died when compare to with those being treated with similar, less expensive medications. The manufacturer of Trasylol, Bayer, has suspended worldwide marketing of Trasylol due to these overwhelming concerns. Some experts estimate that the use of Trasylol could be responsible for as many as 1,000 deaths per month.
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Read more... [Have You Been Harmed By Trasylol?]
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Actavis Totowa LLC in conjunction with the FDA issued a 
