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This is risky because supplements are not regulated with the same rigor as prescription drugs, making it difficult to know exactly how much active compound you are receiving

FDA is aware of some instances in which patients have been given syringes that are significantly larger than the prescribed volume of semaglutide (see example in Figure 1)

The providers gather this information during the patients consultation appointment, allowing them to assess the patient and ensure their eligibility

In a trial enrolling overweight diabetics, hypoglycemia occurred in 4.2% of tirzepatide-treated patients and 1.3% of placebo-treated patients, with tirzepatide-treated patients taking insulin secretagogues having the greatest risk (10.3%)

Torres A, Blasi F, Dartois N, Akova M

The GLP-1 class continues to expand, with even more effective medications expected