ACTOS MDL Established

On December 29, 2011 the Judicial Panel on Multidistrict Litigation (JPML) established MDL No. 2299 for all federal claims alleging injury caused by the diabetes drug Actos.  Actos, manufactured by Takeda Pharmaceuticals America Inc., is the tenth best-selling medication in the U.S. and has been found to increase the risk of developing bladder cancer in…

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Warning renewed for Baby Acetaminophen

The FDA has renewed a warning about the potential for dosing errors with liquid acetaminophen products for infants. FDA advisory committees made recommendations in 2009 that all liquid acetaminophen be produced in a single concentration: 160mg/5mL. The recommendation was voluntary and not all manufacturers have followed it so there are still products with strengths of…

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Multaq Use Limited by FDA

A recent study showed Multaq doubled the risk of heart-related complications in patients with permanent atrial fibrillation. The study, conducted bythe drugmaker,  Sanofi, showed higher rates of heart attack, stroke and death in certain patients. While the FDA did not remove Multaq from the market, they recommended restricting the use of the drug to patients…

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FDA warns HCG diet products are illegal

The Food and Drug Administration last week posted a warning on its website against homeopathic products containing the hormone human chorionic gonadotropin (hCG) that are used for weight loss with severe 500-calories-per-day dieting. The agency also notes that a 500-calorie-a-day diet poses a variety of health risks, including malnutrition, gallstones, electrolyte imbalance and irregular heartbeat.…

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