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The most common adverse events included nausea, affecting 38.1% to 43.2% of treated patients compared to 10.7% with placebo, diarrhea in 33.1% to 34.7% versus 13.4% with placebo, and constipation in 21.8% to 25% compared to 8.7% with placebo

doi:10.1111/jocd.13177

Continuous, uninterrupted use beyond 8 weeks has not been characterized in any published model

The role of peroxisome proliferator-activated receptor gamma coactivator-1 beta in the pathogenesis of fructose-induced insulin resistance

Reduces post-meal glucagon secretion similarly to amylins native function

To lessen discomfort, we keep a careful eye on you and modify your dosage as necessary