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Then, on April 30, 2026, FDA proposed excluding tirzepatide, semaglutide, and liraglutide from the 503B bulks list because FDA did not identify a clinical need for large-scale outsourcing facilities to compound them from bulk substances

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The primary risks include hypoglycaemia (low blood sugar), especially in people with diabetes, and intensified gastrointestinal side effects such as nausea, diarrhoea, and abdominal discomfort

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LAURA: So, since it's a new pen, I need to check the flow