The jury in an Actos bladder cancer lawsuit, last month, found Takeda Pharmaceuticals guilty of destroying documents that may have been crucial to hundreds of lawsuits involving its diabetes medication Actos. While the decision helped plaintiff Richard Myers recover a financial award in the case, … Full Story
Actos® is a prescription medication that is used to help control blood sugar levels in patients with type 2 diabetes. The U.S. Food and Drug Administration (FDA) has issued Actos® warnings due to the dangers of serious side effects. Actos® side effects include an increased risk of bladder cancer and heart failure in some patients.
If you or a family member has been diagnosed with bladder cancer or heart failure after long term use of this medication, you may be eligible to file a lawsuit against the manufacturer. Contact us for more information.
Actos® Drug Information
Takeda Pharmaceuticals is the manufacturer of Actos®. It has been on the market since 1999 and is used for the treatment of type 2 diabetes. It is not intended for the treatment of type 1 diabetes. Actos® works by helping the body make better use of the insulin it produces and stops the liver from producing too much sugar.
Actos® Heart Failure Information
Actos® has been linked to an increased risk of new or worsened heart failure in some patients. When evidence linked the medication to heart failure, the FDA required the manufacturer to include a black box warning about the risk. A black box is the strongest warning that the FDA mandates.
Actos® Bladder Cancer Information
Data has shown a potential risk of bladder cancer in patients who use the medication for long periods of time. The manufacturer is still conducting a study to determine the link between Actos® and bladder cancer. Initial studies which pointed to bladder cancer risks involved rats which developed tumors when given a high Actos® dosage.
Follow up studies have also shown that the risk increases as the level of Actos® dosage and the duration of treatment with the drug increases. The most comprehensive data will be developed during a 10-year study which is currently being conducted by the manufacturer. A 5-year review of the study in 2010 showed evidence of increased risk of bladder cancer in patients that used the medication for more than one year. This has led the FDA to add a warning to the packaging.
A few days before the FDA issued the warning, both France and Germany banned the sale of Actos®, based on a French study that showed the risk of bladder cancer.
Contact an Actos® Attorney
For more information about the risks associated with Actos®, contact an Actos® attorney today.
Despite defendants’ attempts to overturn, a judge has allowed a jury’s $9 billion punitive damage award to stand in an Actos bladder cancer lawsuit filed against Takeda Pharmaceutical Co Ltd and Eli Lilly & Co. Cited in an article featured by Reuters, U.S. District Judge … Full Story
A federal jury ordered Takeda Pharmaceuticals U.S.A. Inc. and Eli Lilly to pay a combined amount of $9 billion in punitive damages for a failure to disclose information about the risk of bladder cancer linked to the diabetes drug Actos. In addition to punitive damages, … Full Story
The number of lawsuit against the makers of the well-known diabetes drug Actos continues to grow as more patients come forward alleging injuries such as bladder cancer. The number of claims is still rising against Takeda Pharmaceuticals, alleging that the drug Actos used to treat … Full Story
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