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A total of 31% of Exelon-treated patients developed at least one episode of vomiting (compared with 6% for placebo). 35 units for 1-4 mg and 6-12 mg of Exelon, respectively. The CIBIC-Plus used in the Exelon trials was a structured instrument based on a comprehensive evaluation at baseline and subsequent time-points of three domains: patient cognition, behavior and functioning, including assessment of activities of daily living. The annualized rate of decline in the placebo patients participating in Exelon trials was approximately 3-8 units per year. At 26 weeks of treatment, the mean differences in the ADAS-cog change scores for the Exelon-treated patients compared to the patients on placebo were 0. They should be urged to read this sheet prior to administering Exelon Oral Solution.

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