Both providers work with 503B outsourcing facilities that operate under FDA oversight, meaning the medication quality standards are comparable between platforms
Additionally, CREDENCE amended their protocol to mandate that participants who developed an active foot lesion were required to interrupt use of the study drug until the lesion resolved (as presented at the American Diabetes Association Scientific Sessions in 2019) (92)
In the SURMOUNT-1 study, in fact, over 95% of participants with prediabetes were able to achieve normalization of blood glucose after 72 weeks of treatment with tirzepatide, the first GIP/GLP-1 receptor co-agonist representing this new class of drugs, compared to 62% of the control group [57]
Patients should avoid injecting into areas with scarring, bruising, inflammation, or skin conditions
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glycaemic control) often play a role in determining the best choice
