Aromatase Inhibitors in Products Marketed as Dietary Supplements
Free Diet Drug Recall Case Evaluation: If you or a loved one has been injured by a dietary supplement containing ADT, you should contact our law firm immediately. You may be entitled to compensation by filing a lawsuit and we can help.
What’s the problem?
September 20, 2010 - The FDA has concluded that products containing aromatase inhibitors (commonly known as ‘ADT’) have a reasonable probability of resulting in permanent impairment of a body structure or function in at-risk consumers.
FDA has notified manufacturers that these products do not meet the definition of a dietary ingredient and therefore are in violation of provisions of the Food, Drug and Cosmetic Act. Many of these products are or had been sold nationwide, both in retail stores and via the Internet directly to consumers. Some have been discontinued but some online retailers may still have remaining inventory that they are offering for sale.
Adverse Events Associated with ATD
Products marketed as dietary supplements contain ATD. Adverse events associated with the use of aromatase inhibitors could include the following:
- decreased rate of bone maturation and growth
- decreased sperm production
- aggressive behavior
- adrenal insufficiency
- kidney failure
- liver dysfunction
Consumers with liver, kidney, adrenal, or prostate abnormalities are at higher risk for developing adverse events. Consumers who have any of these products in their possession should stop using it immediately. If consumers experience any adverse side effects due to its consumption they should contact a physician.
Do I have a Dangerous Diet Drug Recall Lawsuit?
The Defective Drug & Products Liability Litigation Group at our law firm is an experienced team of trial lawyers that focus on the representation of plaintiffs in ADT diet drug recall lawsuits. We are handling individual litigation nationwide and currently accepting new cases in all 50 states.