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Congress requires "sound science" from FDA on ephedra proposal |
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| A May 13 addition to the House budget bill requires FDA to employ "sound science" and a rational analysis of adverse events, before proceeding with ephedra rulemaking. The amendment was offered by Rep. Sam Farr (D-CA). The FDA issued its proposed rule to limit per-serving and per-day intake of ephedrine alkaloids for supplements in June, 1997. | ||
| The Tan Sheet, May 17, 1999. | ||
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