Januvia Class Action Lawsuits vs. Januvia MDL

Januvia, a drug approved in 2006 by the FDA to be used in the treatment of Type 2 diabetes, has been found to bring a risk of pancreatitis, pancreatic cancer and thyroid cancer among users. Reports of 88 serious cases of pancreatitis were sent to the FDA between the time Januvia was approved and 2009. Of these 88 cases, over half resolved when Januvia was discontinued. At least one-fifth of the patients had only been taking Januvia for a month or less and 75% of the patients required hospitalization. 

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Pradaxa (Dabigatran) and the FDA Safety Review

Although only on the market for a relatively short period of time, Pradaxa, the blood-thinning drug manufactured by Boehringer Ingelheim—has already suffered under the weight of threatened recalls, lawsuits and warnings by the FDA. Pradaxa is the first FDA-approved drug of its type since the drug Warfarin was approved in 1954.
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Actos Discussions: Dangers of the Drug

Links to higher heart disease rates have been associated with the use of Actos, and, in fact, Actos may cause as many heart problems as GlaxoSmithKline’s drug, Avandia. The American Heart Association reported that studies showed patients taking either diabetes drug were at least four times as likely to experience heart attacks, heart failure or even death.
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Actos Discussions: Your Actos Case

Hundreds of thousands of patients who have taken the drug Actos over the past few years—believing the drug to be safe—have been very disillusioned to find that the drug can have some potentially very serious side effects. Actos is a drug which was developed for the treatment of Type 2 diabetes and works by helping the body restore its normal response to insulin, effectively lowering blood sugar.
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