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A morning dose aligns with the bodys natural detox cycle
Oral bioavailability for Dihexa has been estimated at 4060% in animal models, substantially higher than most peptides which typically show less than 5% oral absorption due to first-pass metabolism and enzymatic degradation in the gastrointestinal tract
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A review of GLP-1 agonist studies using the standard dose in high intracranial pressure reported: Patients should be counseled about the high likelihood of nausea and GI upset (diarrhea, vomiting, and constipation, delayed gastric emptying) especially in the first 48 weeks of therapy
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