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             Drug Effectiveness Review Project













                                       29% of TAC treated patients had three times the upper limit of normal (120 U/L)














                                              Significantly higher rate of  ALT elevations in TAC group
                                                                                          placebo      11%
                                    54% of TAC treated patients had elevated ALT levels
                                           90% of elevations occurred within the first 12 weeks











                                                           Post randomization exclusions:
                                                                                   Overall loss to follow-up: 58%






                                                                                          tacrine  Loss to follow-up differential high:       55%    Primary reason: ALT   elevations; also gastrointestinal   symptoms (16%)






                                                        ITT: Yes                                                    Poor




                                                               Yes      NR   Yes














             Final Report Update 1     Authors: Knapp et al.   Year: 1994   ADVERSE EVENTS:            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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