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Adhering to a controlled dosage escalation, patients start at a lower dose, allowing healthcare providers to facilitate increases based on individual response

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While using SEMGLEE do not: drive or operate heavy machinery, until you know how SEMGLEE affects you

SELECT Trial Result: A primary cardiovascular end-point event occurred in 6.5% of semaglutide patients versus 8.0% of placebo patients a hazard ratio of 0.80, representing a statistically significant 20% reduction in major adverse cardiovascular events (MACE)

If you are in this space, you already know the zero-citation problem is real