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Why Hydroxycut Had to Kill Someone Before the FDA Could Act

By Jim Edwards | May 4, 2009

The FDA has moved to ban diet aid Hydroxycut after it received 23 reports of serious health problems and one death due to liver failure.

The recall points out the ridiculous position of federal law as it relates to diet supplements: Even though the FDA has sweeping powers to ensure the safety of drugs and food through its approval and inspection process, it has almost no power over the “diet supplement” industry.

The Dietary Supplement Health and Education Act of 1994 specifically removes FDA authority over the pills sold by GNC, Vitamin Shoppe, Herbalife, et al. It says:

… the Federal Government should not take any actions to impose unreasonable regulatory barriers limiting or slowing the flow of safe products and accurate information to consumers … [unless a product] presents a significant or unreasonable risk of illness or injury …

Thus — unlike with meat, eggs, spinach, tomatoes or Lipitor – the FDA is limited to waiting until people actually die before the law permits it to inspect and ban a product. Which is exactly what has happened in the Hydroxycut case. The FDA said:

The FDA has received 23 reports of serious health problems ranging from jaundice and elevated liver enzymes, an indicator of potential liver injury, to liver damage requiring liver transplant. One death due to liver failure has been reported to the FDA. Other health problems reported include seizures; cardiovascular disorders; and rhabdomyolysis, a type of muscle damage that can lead to other serious health problems such as kidney failure.

Note that Hydroxycut was not on the list of banned/dangerous diet drugs that the FDA wanted pulled from shelves back in January, thus proving how little power the FDA has over diet supplements.

The diet supplement industry’s lobby group, the Council for Responsible Nutrition, wants the law to become even more relaxed. It is currently lobbying the FTC to give it the right to make false statements in ads so long as nobody could be expected to believe those statements. Its official position is:

An advertising claim that you don’t believe can’t hurt you.

Meanwhile, with the diet supplement industry an official wild west of dubious claims and big profits, big drug companies such as Bayer and Wyeth.

Jim Edwards, a former managing editor of Adweek, has covered drug marketing at Brandweek for four years, and is a former Knight-Bagehot fellow at Columbia University's business and journalism schools. Follow him on Twitter or send him an email.

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Web Buzz:
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    WASHINGTON ? Supermarkets and other retail outlets that sell dietary supplements have begun accepting returns of various Hydroxycut products, following a voluntary recall announced Friday by the manufacturer. The recall of the popular weight-loss/energy-enhancement aids were implemented after the Food and Drug Administration determined the...

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    Ever since news broke about a US recall of weight loss products called Hydroxycut, the one-man industry regulator Dr Ken Harvey has been on a campaign to get some action in Australia. The Food and Drug Administration says the supplements have been associated with serious side effects, including liver toxicity. InCanada, a class action law...

  • Warning against Hydroxycut diet pill

    Sky News - 190 days 2 hours 28 minutes ago

    Dieters who use the weight loss and energy-boosting Hydroxycut supplements should immediately stop, the US drug regulator says after reports of liver injuries and one death. One person had died from liver failure, the US Food and Drug Administration (FDA) said. The agency has received 23 reports of liver problems linked with use of the products,...

 

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