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In the agencys own words, it does not have the authority to approve dietary supplements for safety and effectiveness, or to approve their labeling, before the supplements are sold to the public.3 This means that its up to supplement manufacturers to take the necessary steps to ensure consumer safety

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These reports reflect controlled laboratory conditions only and do not translate to dosing, treatment, or applications in any other context

That study could also determine biomarkers such as cortisol, coagulation, KP metabolites and the cytokines elevated in PCS, both before and during SSRI use

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The LID-specific elevation of certain PUFA-containing GPLs positively correlated with LID scores, as well as with L-DOPA and dopamine levels