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Journal of Physiology-Paris, 94(2), 139151

Simple answer, Yes

And so FDA is going to need to use a different lens. Unlike FDA approval of a new drug, which requires years of clinical trials demonstrating safety and effectiveness, placement on the 503A Bulks List answers a different regulatory question

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DHEA is a hormonal supplement that should only be taken under medical supervision

The examination reveals the bilateral, symmetrical nature of nodules and helps distinguish them from other lesions such as polyps, cysts, or edema