Weight loss supplements under Hydroxycut banner withdrawn: death, liver failure – where will this end?

FDA and the New York Times are reporting today 23 cases of adverse reactions to various Hydroxycut weight loss supplements. (FDA Consumer PDF here).
Above and beyond whether the stuff actually helps with weight loss, it is clear that the products contain some compound(s) that cause idiosyncratic cases of liver damage.

According to the law governing dietary supplements, the F.D.A. is empowered to act only in cases when it identifies a harmful or adulterated product that is already on sale.
“Part of the problem as you know is that F.D.A. looks at dietary supplements from a post-market perspective, so that an isolated incident is often difficult to follow,” Dr. Linda Katz, interim chief medical officer of the agency’s Center for Food Safety and Applied Nutrition, said Friday during a conference call with reporters.

And this is what gets my goat about the 1994 Dietary Supplement Health and Education Act (DSHEA) and something that the new FDA chief (and consumers) should really try to cultivate Congressional support to change:

In March, the federal General Accounting Office issued a report (77 page PDF) that criticized federal oversight of dietary supplements. The report, commissioned by the House Committee on Energy and Commerce, concluded that the F.D.A. had insufficient knowledge of the dietary supplement industry, insufficient resources dedicated to overseeing the industry, and insufficient ability to identify and recall problem products.

Enough already.

8 thoughts on “Weight loss supplements under Hydroxycut banner withdrawn: death, liver failure – where will this end?

  1. I urge anyone that has been using this product to A: contact your physician B: contact a good attorney, these mutts at Hydroxicut have been hyping this product while all along knowing that the product was not only bogus in it’s claims but harmful to consumers and deserve to be sued by any consumer who was effected by their product.

  2. Isn’t that (more or less) what Congress asked for? If you allow people to claim the sun and moon for their products (without evidence) and you don’t provide the resources or authority to deal with the makers of drugs you have told the FDA to regulate, then where are you expecting the FDA to come up with the attention, authority, or cash to deal with supplements?
    This isn’t even an unintended consequence of the law, but a pretty easily anticipatable one.

  3. I just got another FDA warning that over 30 ‘weight loss’ agents from universal ABC beauty supply international, NY, have been pulled because they all contain sibutramine.
    The law has to be changed on this. It is a multi-billion dollar industry; why shouldn’t they have to follow the same rules as the pharmaceutical industry does?

  4. The FDA has a tough line to walk to try and get medications to people that can receive benefit, but not so early as to miss major problems. When side effects occur only in 0.1% of the subjects, you need to have 10s of thousands of subjects to really see it become statistically significant from placebo. Yes, it is sad that this happens, but there is just no way to prove that drugs are conclusively safe before they are approved.

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