PPA
Phenylpropanolamine (PPA) was a widely used "active ingredient" in over-the-counter, and some prescription, cold and allergy products. PPA was also used as an "active ingredient" in many over-the-counter diet pills. In total, it is estimated that PPA was the active ingredient in over 400 products sold to the consuming public, in an estimated 6 billion doses sold annually.
On November 6, 2000, the Food and Drug Administration issued a Public Health Advisory concerning PPA, and its use as a nasal decongestant and for weight control. In doing so, the FDA began the process of having PPA-containing products removed from the market. The FDA's bold consumer protection action in having PPA removed from products was based on the association between phenylpropanolamine and hemorrhagic stroke that was established in the industry funded Yale Hemorrhagic Stroke Project, published in the prestigious New England Journal of Medicine.
If you or a loved one is in need of legal assistance, call The Law Offices of Alan R. Goodman at 1-413-736-1616 or submit an online questionnaire. The initial consultation is free of charge, and if we agree to handle your case, we will work on a contingency fee basis, which means we get paid for our services only if there is a monetary recovery of funds. In many cases, a lawsuit must be filed before an applicable expiration date, known as a statute of limitations. Please call right away to ensure that you do not waive your right to possible compensation.
|
Resources Center for Drug Evaluation and ResearchDoctor's GuideFDA U.S. Pharmacopia Medwatch |