Call Our Experienced Dangerous Drug Lawyers in Indiana
If you or a loved one suffered severe side effects, including the development
of bladder cancer, after taking Actos, you may be able to seek compensation
for damages. Recent studies have revealed the severe health risks of Actos,
leading the FDA to release a black box warning for possible congestive
heart failure. Over the past few years, the drug manufacturer, Takeda,
has received thousands of lawsuits for failure to conduct adequate research
and for negligence.
What is Actos?
Actos, the brand name for the drug pioglitazone, is a medication prescribed
for the treatment of Type II Diabetes. Actos was designed to lower blood
sugar by decreasing insulin levels and reducing glucose production in
the liver. It is administered orally once a day, and in varying doses
in correlation to the need of the patient and the discretion of the prescribing doctor.
The FDA approved of distribution in 1999 and Actos has since been one of
the most popular diabetes medicines and best-selling diabetes drug in
the nation. Years later, the FDA began reviewing studies of individuals
who developed bladder cancer at an unusually high rate after taking Actos
for a period of more than one year.
Dangerous drug Actos has been linked to numerous dangerous side effects, most prominently
congestive heart failure, liver failure, and the increased risk of the
development of bladder cancer. Severe side effects of Actos include:
- Congestive heart failure
- Increased risk of bladder cancer
- Liver failure
- Chronic kidney disease
- Bone fractures, especially in the hands, feet, and ankles
- Upper respiratory infection
Warnings and Medical Studies
In 2011 the FDA issued a warning based upon these studies that Actos may
be linked to an increased risk of the development of bladder cancer for
individuals using the drug for one year or more. Since these warnings
have been released, health authorities in both German and France have
suspended all use and sale of Actos because of the increased risk of the
development of bladder cancer. The FDA has recommended that physicians
not use pioglitazone in patients with active bladder cancers or a history
of bladder cancers and urged that the benefits of the drug must be weighed
against these risk factors in such patients.
There is current litigation against the manufacturer of Actos, Takeda Pharmaceuticals,
filed by people who developed bladder cancer after taking Actos for an
extended period of time. When this drug was placed on the market, it is
alleged that insufficient warnings existed to inform patients of these
potential health risks and concerns.
If you or your loved one has been diagnosed with bladder cancer and has
taken the drug Actos for a period of more than one year prior to the diagnosis,
contact George & Farinas, LLP today to discuss your rights and how to file a product liability case.