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The FDA could view the wide-scale manufacturing of custom medications as taking advantage of loopholes that ought to be closed: I suspect the FDA never contemplated that [its guidance] would be applied the way it's being applied, given the scale of the compounded GLP-1 phenomenon, he says

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Regulators update labeling on their own timelines as postmarketing data accumulate, so a safety subsection that has been revised or removed in one country's label may still stand in another's