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Disparities in the quantity and percentage of the documented psychiatric AEs among different GLP-1 RAs could potentially be associated with factors such as their duration in the market (e.g., more time for AEs to be reported into FAERS for medications that have been available for longer), clinical utilization, and specific drug characteristics

These overlapping effects not only inhibit tumour initiation and early progression but also render conventional therapies more efficacious sensitizing tumour cells to chemotherapy-mediated apoptosis, protecting normal tissues against radiation-induced oxidative damage, dampening chemotherapy-associated inflammation (e.g

doi: 10.1016/j.cell.2022.02.011

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