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Adverse Event Reporting

Industry experts are proclaiming victory in getting a law passed that requires dietary supplement (and OTC drug) manufacturers to report all serious “adverse events” to their products to the FDA. With the obvious bias in the media against supplements, each reported (but not proven) “reaction” will likely be used to hammer dietary supplements.

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Pandering to FDA

What’s up with the supplement industry associations rolling over for FDA on ephedra? When the FDA announced the ban on ephedra, industry ‘thought leaders’ couldn’t jump fast enough to say what a wonderful thing it was. The industry line is that the FDA banning a plant that’s been in use for over 5,000 years, based […]

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