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We present a case of a 48-year-old woman with type 2 diabetes, who developed persistent nausea and vomiting after resuming semaglutide at 2 mg subcutaneously once weekly without following the recommended stepwise titration schedule (typically initiated at 0.25 mg weekly with gradual escalation)

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Are the problems a coincidence or related to the drug?

This suggests that no dose adjustments should be required when semaglutide is administered concomitantly with these medications.

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