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Although the drugs are similar and both had FDA warnings in 2007, Takeda's Actos has been perceived to be safer for the treatment of type 2
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In 2007, the FDA ordered Takeda Pharmaceuticals, the manufacturer of Actos, to include a black-box warning on its product. The warning explained that Actos
The FDA first mandated that Actos should carry a black box warning in June of 2007. The FDA cannot dictate such a warning, which is then
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In June 2007 the FDA required the manufacturers of Actos and a similar-acting drug, Avandia, to add a "black box" warning to the drugs'
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Actos® is in the thiazolidinedione class of drugs, which have been found to cause, or worsen, heart failure. Since 2007, the warning label containing the
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A black box warning of the danger of congestive heart failure that may be exacerbated or caused by Actos® was added to the drug's label in August 2007.
Although Actos first hit the prescription drug market in 1999, there is mounting evidence of a link between Actos and bladder cancer. Since 2007, it has been the
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