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Consumer OTC Drugs

FDA Considering "Numerous" Ephedra Adverse Events In Rulemaking

This article was originally published in The Tan Sheet

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Executive Summary

FDA will take the "numerous adverse events" related to ephedra that continue to be reported to the agency into consideration as it develops rulemaking on the substance, FDA Commissioner Jane Henney, MD, said at a budget hearing of the House Agriculture Appropriations subcommittee Feb. 23.

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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