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The most commonly reported adverse events (observed in greater than 5% of clinical trial participants) were nausea, diarrhea, vomiting, constipation, abdominal pain, dyspepsia, injection-site reactions, fatigue, hypersensitivity reactions, eructation, hair loss and gastroesophageal reflux disease

Current medicinal chemistry , 31 (29), 4579-4601

After the first month or two of introductory lower doses, hunger seriously abates or becomes non-existent

In addition to the key trends detailed in the report, MedOne outlines additional market changes that have had a significant impact on the prescription benefit landscape

Minna Kim (www.stamfordnaturopathic.com)