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             Drug Effectiveness Review Project






























                                 placebo      72.0%   4.5%   9.4%   5.9%                            placebo      16%   6.9%








                          Authors and Year: Tariot et al. 2000; Cummings et al. 2004; Galasko et al., 2004












                                 galantamine   8; 16; 24 mg/d   75.5%; 73.8%; 80.2%   5.7%; 13.3%; 16.5%   15%;10%; 8.1%   5%; 12%; 5.5%   Post randomization exclusions:  NR   Overall loss to follow-up: 20.7%  Loss to follow-up differential high:  Yes   galantamine   8; 16; 24 mg/d   22.8%; 21.5%; 22.3%   6.4%; 6%; 9.8%












                                                          NR       ITT: Yes   Yes      Yes    Yes                       Fair
















             Final Report Update 1        ADVERSE EVENTS:      Overall adverse effects reported:   Nausea   •   Agitation   •   Diarrhea   •     Significant differences in adverse   events:      ANALYSIS:    ADEQUATE RANDOMIZATION:   ADEQUATE ALLOCATION   CONCEALMENT:  BLINDING OF OUTCOME   ASSESSORS:   ATTRITION (overall):     ATTRITION (treatment specific):      Loss to follow-up:   Withdrawals due to adverse events:        QUALITY RATING:      *primary outcome measures     Alzheimer's Drugs
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