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However, many of these articles primarily provide descriptive overviews of phytochemicals or focus predominantly on preclinical mechanistic findings without systematically integrating translational, clinical, pharmacokinetic, and safety dimensions within a single framework

Additionally, the study found that resmetirom was safe and well-tolerated, with no significant difference in the primary endpoint of incidence of treatment-emergent adverse events between the groups

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Following the release of a drug, the FAERS database collects adverse events reports from providers and patients that are witnessed in-market (i.e., in the real world practice of medicine rather than during a clinical trial or drug testing process)