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[1] [2] The European Medicines Agency's European Public Assessment Report (EPAR) for Ozempic does not specifically highlight dysgeusia as a common adverse event in clinical trials

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Maintaining the protocols nutritional framework even after side effects resolve is essential for maximizing the 48-week trajectory

There is interest in their use in non-alcoholic fatty liver disease (NASH), as they have shown improvements in liver enzymes and histology in trials (e.g., semaglutide in NASH)

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