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Pilot clinical studies and case reports describe nausea in 65% of subjects at doses above 0,5 mg (resolution 2-4 h post-injection), flushing in 55%, transient increases in blood pressure and tachycardia in 40-60% of subjects, with peak acute effects occurring 90-120 minutes post-dose
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Pediatric may result in elevated blood concentrations of vitamin E and potential vitamin E toxicity [see Warnings and Precautions (5.8)]
Diabetes Care 2025;48:S181206.
[1] In the SURMOUNT clinical trial program, which included over 5,000 participants across multiple studies, anxiety was not identified as a common or notable side effect
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