**Overview** The Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS) data package contains information on medication errors, quality complaints a
This is a multicenter, double-blind, placebo controlled, randomized, outpatient, multiple dose study in male and female patients ages 50 to less than 89 years with mild to moderate AD. Approximately 2
ADE = adverse drug event; CI = confidence interval. aAs one person could have multiple ADEs, the combined prevalence is lower than the sum of the prevalences of the ADE categories. bSelf-reported use