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Hydroxycut(R) Litigation Focus of July 28 Conference in San Francisco
Date:6/12/2009

mas Clark said during a recent HB teleconference that from January to October 2007, there were 298 adverse event reports made to the FDA regarding dietary supplements. That number grew to 948 for the same period in 2008. Of those reports, Clark said, 596 were mandatory reports by the industry. The FDA estimates that there are 50,000 adverse events from dietary supplements each year, but less than 5% of these are being reported, Clark explained. "This rises to a whole new level of under-reporting," he said, in part because individual consumers either do not connect their symptoms with the supplements or do not tell their doctors they are taking them.

Dr. Andrew Klein, MD, FACS, MBA, director of the Comprehensive Transplant Center at Cedars-Sinai in Los Angeles and David Vermont of Ashcraft & Gerel in Washington, D.C., will provide a review of the medical and scientific aspects of liver, kidney and cardiovascular injuries, alleged to be caused by these supplements.

Lori Andrus of Andrus Anderson in San Francisco and Robert Gordon of Weitz & Luxenberg in New York will provide a perspective on case screening, client retention, case management, and medical record review and testing.

Iovate itself says that it has more than 750 items sold in more than 70 countries, and they "undertake extensive medical, scientific and toxicological literature reviews on the safety of the ingredients during the development stage of each product. Additionally," a May 1 statement from the company continues, "third-party experts from the leading independent scientific firm specializing in ingredient assessment, toxicology and product safety for the nutritional and pharmaceutical industry review the safety of Iovate's ingredients and formulas before products are introduced in the marketplace. Only after this external review is completed does Iovate release a formula."

An article written for Calliope Media
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SOURCE HB Litigation Conferences
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