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Through the FDA Adverse Event Reporting System (FAERS), healthcare providers and patients can report suspected adverse events, including potential malignancies, enabling the agency to detect safety signals that may not have been apparent in pre-approval clinical trials
However, with the lack of data on bone condition, including BMD, microarchitecture, bone quality, calcium, and phosphorus levels at baseline in this study, the results should not be taken as definitive
(B) Schematic diagram of a GLP-1 tandem-repeat construct (6mGLP-1)