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Migratory fate and differentiation of blood monocyte subsets

If liver risk appears more advanced, additional testing or specialist involvement may be recommended

Pre-Approval Clinical Trial Data The clinical trials that led to FDA approval showed: High rates of nausea, vomiting, and abdominal pain among participants Documented cases of severe gastrointestinal issues requiring medical treatment Evidence that slowed gastric emptying persisted in some patients Reports of adverse event reports related to digestive system paralysis Despite this significant evidence from clinical trials, Novo Nordisks labeling focused on common, temporary side effects while failing to warn patients about the risk of permanent gastroparesis

However, the authors were unable to assess the incidence of FG or whether SGLT2 inhibitors were causative

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The following information is based on the company's published terms and website as of December 26, 2025