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If you experience persistent vomiting or diarrhoea while taking GLP-1 medications, seek medical advice as this could lead to dehydration and electrolyte disturbances

In 2018, FDA published guidance to 503A pharmacies on what will be considered unauthorized compounding of a product that is essentially a copy of an FDA-approved product, with an exception available when the prescriber documents on the prescription that the compounded drug product produces a significant difference for the identified individual patient. Under the 2018 guidance, FDA generally does not intend to question prescriber determinations that are documented in a prescription or notation. To date, patient-specific GLP-1 compounding activities have often included adding supplemental ingredients to combat side effects of the GLP-1 products or customizing doses, with a significant percentage of prescriptions for customization written by telehealth prescribers

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GLP-1RA significantly reduced the risk of heart failure by 10% and all-cause mortality by 12%

If you are not losing weight on tirzepatide at your current dose, discuss options with your provider rather than self-adjusting

Why is my pharmacy's label more authoritative than the ranges I read online