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Additional warnings in the FDA prescribing information include: severe gastrointestinal adverse reactions, acute kidney injury, acute gallbladder disease, acute pancreatitis, serious hypersensitivity reactions, hypoglycemia risk when used with insulin or insulin secretagogues, diabetic retinopathy complications and vision changes in patients with type 2 diabetes, depression or mood changes requiring clinical monitoring, and pulmonary aspiration risk during general anesthesia or deep sedation

and change from baseline to week 104 in pulse, amylase, lipase and calcitonin

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This chart shows clinical trial protocols from published studies

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