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Incidence in Controlled Clinical Trials The table that follows enumerates adverse events that occurred at a frequency of 1% or more among BuSpar (buspirone hydrochloride) patients who participated in 4-week, controlled trials comparing BuSpar with placebo

Both are set by Eli Lilly and apply uniformly across all dose strengths (2.5, 5, 7.5, 10, 12.5, 15 mg)

This integrated approach allows researchers to study greater and more sustained weight-loss mechanisms compared to therapies that focus only on appetite suppression

Wirth PJ, Shaffrey EC, Bay C, Rao VK

Clear documentation of medical necessity and patient education about realistic weight loss expectations strengthens prescribing decisions