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A comprehensive safety and tolerability study evaluated approximately 900 participants across six trials with the following protocols: Subcutaneous/Intravenous Protocols: Single doses ranging from 25 to 400 mcg/kg body weight were tested
In addition, this was supplemented by Gastrointestinal Symptom Rating Scale (GSRS)-IBS before and 12 weeks after LFD
Talebizadeh Z, Butler MG
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Oltre alla significativa efficacia sullomeostasi glicemica, alcuni membri di questa categoria di farmaci trovano inoltre indicazione nel trattamento dellobesit
