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"Edward Kennedy, September 10,1997,at Senate hearings on the fda reform Bill More than three decades ago, consumer advocate Ralph Nader made one of the first public declarations about how thoroughly the cosmetics safety deck is stacked in favor of manufacturers and against the buying public. "The FDA claims to see great advantages in voluntary [industry] actions ?flexibility, speed, and low costs to the FDA," Nader wrote in a chapter about cosmetics safety for the 1974 book Consumer Health and Product Hazards, published by MIT Press (a book I co-edited). "
- Samuel S. Epstein, Randall Fitzgerald, Toxic Beauty: How Cosmetics and Personal Care Products Endanger Your Health . . . And What You Can Do about It (Get the book.)

"Reputation of the FDA in Shambles after Vioxx Scandal; Calls for Wholesale fda reform, , 11/10/2004. • American Consumers Suffering as More New Drugs Debut in US, Analysis Shows, Pugh and Borenstein, Knight-Ridder, 12/18/2004. • FDA Delays Response to Drug Suit, , Associated Press, 11/4/2004. • "Risk-Free" Drugs Don't Exist, Business Week Online, 2/23/2005. • Testimony of Barbara Atkinson, MD on House Bill 2355, KUMC Campus News, 3/17/2005. • FDA to Review "Missing" Drug Company Documents, Jeanne Lenzer, , 1/1/2005."
- Brent Hoadley, Ph.D., Too Profitable to Cure
(Get the book.)

"Horton was outraged and called for FDA reform: "In the case ofVioxx, the FDA was urged to mandate further clinical safety testing after a 2001 analysis suggested a 'clear-cut excess number of myocardial infarctions.' It did not do so. This refusal to engage with an issue of grave clinical concern illustrates the agency's in-built paralysis, a predicament that has to be addressed through fundamental organizational reform." But Dr. Horton didn't stop there. He also explained, "...with Vioxx, Merck and the FDA acted out of ruthless, short-sighted, and irresponsible self-interest."
- Mike Adams, Natural Health Solutions (Get the book.)

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