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This limited oversight and lack of FDA approval exposes patients to several clinical risks: Contamination and impurities: Federal regulators and manufacturers documented critical sterility failures in compounded formulations during laboratory testing
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This launch is expected to improve affordability and access, allowing broader patient adoption and giving payers a cost-effective alternative amid rising demand for obesity treatments
The transcriptomic datasets used for the study were obtained from NCBI Gene Expression Omnibus (GEO)
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