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Published online 2 April 2004 | Nature | doi:10.1038/news040329-17

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Experts rethink vitamin safety

Manufacturers should report ill-effects of herbal supplements report says.

The makers of dietary supplements should be forced to notify the US Food and Drug Administration (FDA) of adverse events, according to a new report.

The report is designed to tackle growing unease in the United States about the safety of certain herbs, vitamins and other products often taken as tonics.

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