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These include a limited sample size (N = 64), the lack of statistically significant differences in primary outcome measures, a narrow efficacy profile, a brief treatment duration, and the inability to isolate independent therapeutic effects due to its adjuvant nature
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When microdosing is discussed outside this sequence, it becomes a tactic without a strategy
But its a game of whack-a-mole: New sites pop up all the time, and neither the NABP nor the FDA has reviewed them all
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