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→ Most participants in trials reached 8–12 mg weekly, which delivered the strongest results → Dosing protocols may be refined in Phase 3 and post-approval, but gradual titration will remain the standard
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mg:10mg x 10 vials
Further, the FDA criticizes the loophole created by the “ adequate provision ” requirement (1997), a provision requiring drug advertisements for TV and radio to direct consumers to separate sources for complete drug risks and safety facts
