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Actos - Dangerous Drug Report

Actos - Dangerous Drug Report

The product liability attorneys at SHOOP | A PROFESSIONAL LAW CORPORATION warn again of the dangers and side effects associated with prolonged usage/ingestion of the prescription drug, Actos. This is a drug that was typically prescribed to individuals suffering complications from Diabetes.

For numerous of those individuals who have been prescribed this medication, it has also been associated with severe and/or fatal side-effects. If you or anyone in your family has suffered illnesses more particularly described below, or if any family member or loved one has died after prolonged ingestions of the diabetes drug Actos, please contact the attorneys at SHOOP | A PROFESSIONAL LAW CORPORATION to discuss your legal rights.

Side Effects Associated with Actos

The side effects associated with the use and ingestion of Actos are numerous, and include, but are not limited to, the following medical issues:

1. Renal (Kidney) Failure

The United States Food and Drug Administration "FDA" has reported potential safety issues and medical complications with regard to renal failure subsequent to prolonged, Actos usage. This has been linked to a condition known as "Rhabdomyolysis" which is a physical condition that brings about deterioration of muscle tissue and fibers, which, in turn, causes a release and introduction of myoglobin into the bloodstream. Symptom-otology associated with this condition include:

  • muscle weakness;
  • fever;
  • fatigue; as well as
  • pain, nausea and vomiting.

As these symptoms are associated with and indicative of potential renal failure as well as other, related issues, it is of prime importance that you contact your doctor ASAP should you experience these symptoms while on Actos.

2. Heart Attack Risk

Helen Ge, M.D., a former Pharmaceutical Consultant for the drug manufacturer, Takeda Pharmaceuticals, is a whistleblower that reported the company's failure to address Actos issues related to heart attacks, and the allegations that the company failed to report, as required by federal law, adverse events to the FDA Maude database.

3. Cancer of the Bladder

The FDA has further issued medical reports linking Actos use as causative of increased risk of bladder cancer to individuals on Actos. This risk increases exponentially when the drug has been ingested for more than a year (or more). It is expected that this will be added to a black box warning within the near term. Several European nations have already suspended sales of the drug.

The product liability attorneys at SHOOP | A PROFESSIONAL LAW CORPORATION continue to accept Actos cases. If you or anyone in your family has suffered an Actos-related injury or side effects, you need experienced legal counsel with significant experience in drug and device matters. Contact SHOOP | A PROFESSIONAL LAW CORPORATION today to speak with an experienced attorney.

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