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As of June 30, the FDA Adverse Event Reporting System (FAERS) has received 59 reports of suicidal ideation, six reports of attempted suicide, and four reports of suicide-related to Ozempic

Food and Drug Administration (FDA) for the management of blood sugar levels in type 2 diabetes

The inconsistencies observed may be attributed to factors such as limited sample sizes, insufficient paid to blood glucose fluctuations,and patient heterogeneity, including variations in islet function and single nucleotide polymorphisms (SNPs) within the incretin-related genes