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When a biosimilar is approved based on a clinical program in one indication, the FDA may approve it for all indications held by the reference biologic without separate clinical trials in each, provided the mechanism of action is the same and there is no scientific reason to expect differential clinical behavior across the populations

Dietary measures are first implemented in individuals with significant side-effects

Children and adolescents are not small adults

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Here is the suggested 6-month Tirzepatide titration plan: The following chart shows the dosage schedule, and can be useful for your treatment plan