Usage of the Diabetes Drug, Actos, Sparks Lawsuits Across the Country
Earlier this week, we brought you news regarding the diabetes drug, Actos, and how Americans were becoming more aware of a very dangerous potential side effect – bladder cancer. Well, things don’t appear to be looking up for Japanese Manufacturer, Takeda Pharmecutical Industries Limited (“Takeda”).
Whistle Blower Lawsuit
Earlier this year, U.S. District Judge F. Dennis Saylor reportedly issued an order to unseal a whistleblower case (Case 1:10-cv-11043-FDS) by a former medical reviewer in Takeda’s pharmacovigiliance division. Medical reviewer, Dr. Helen Ge, alleged that Takeda told medical reviewers to “change their professional opinion” regarding assessing certain reports of bladder cancer for FDA reporting. Apparently Takeda’s database for adverse events for Actos held more than 100 bladder cancers reported to the company; however, only 72 were reported to the FDA. Dr. Ge says she was fired when she raised the question about the discrepancies and Takeda’s general reporting practices.
Products Liability Lawsuits
To further add fuel to the fire, last week the US Drug Watchdog sent out an urgent call to individuals who were diabetics, took Actos, and were diagnosed with bladder cancer. This knowledge has since sparked some 10,000 lawsuits across the country.
The Western District of Louisiana is currently handling the multidistrict litigation for all federal claims alleging injury caused by Actos (In Re: Actos (Pioglitazone) Products Liabilty Litigation No. 6:11-md-2299). However, other cases have sprung up around the country as well.
Takeda’s Profits Take a Hit
In 2010, Actos ranked number nine in the top 10 selling prescription drugs in the country with sales of $3.5 billion.
These lawsuits, coupled with generic versions of Actos now being manufactured and sold by other companies, prompted sales of Actos to decrease 46.2 percent in 2012 from the previous year. From 2011 to 2012, Takeda estimated that sales of Actos will decline 67 percent. This loss is significant as Actos sales reportedly contributed up to 20 percent of Takeda’s 2011 revenue. In July 2012, the company’s stock fell to an 11-year low.
Remember to discuss your medication options with your health-care provider before stopping any current medications. But, if you’ve taken Actos and have experienced serious ailments, such as bladder cancer, you should seriously consider talking to an attorney about your condition.
The information on this page is meant to provide a general overview of the law. The laws in your state and/or city may deviate significantly from those described here. If you have specific questions related to your situation you should speak with a local attorney.
Additional Actos Articles
- Dangerous Drugs and Product Liability Law
- Drug Actos Under Fire for Allegedly Increasing Risk of Bladder Cancer
- Defective Drug Warning Labels and Off-Label Use
- What Is Actos?
- Why Are There Problems With Actos?
- Are there other drugs like Actos?
- What Is Type 2 Diabetes?
- Why was there an FDA recall of Actos?
- Are People Who Take Actos At A Higher Risk Of Broken Bones Or Fractures?
- Is It True That Someone Who Took Actos Has A Higher Rate Of Heart Attack Or Heart Failure?
- Has there been an FDA review of Actos?
- Has There Been An Actos Recall?
- Is Actos associated with serious side effects?
- Why did the FDA require Actos to update their label?
- Is it true that bladder cancer has been associated with using Actos?
- What are the results of FDA’s safety review of Actos?
- Should I settle my Actos lawsuit?
- How can you get an Actos settlement?
- How long do I have to file a lawsuit against Takeda Pharmaceuticals?
- What is a black box warning?