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. 2021 Mar 26;21(5):535–543. doi: 10.1007/s40256-021-00464-y

Table 2.

Summary of death, dropout, and cardiovascular-related hospitalization visits

Event Placebo (n = 177) Tafamidis 20 mg (n = 88) Tafamidis 80 mg (n = 176) Pooled tafamidis (n = 264) All patients (n = 441)
All-cause mortality 76 (42.9) 24 (27.3) 54 (30.7) 78 (29.5) 154 (34.9)
Dropouta 50 (28.3) 14 (15.9) 32 (18.2) 46 (17.4) 96 (21.8)
CV-related hospitalizations
 0 70 (39.5) 46 (52.3) 80 (45.5) 126 (47.7) 196 (44.4)
 1 53 (29.9) 22 (25.0) 46 (26.1) 68 (25.8) 121 (27.4)
 2 23 (13.0) 10 (11.4) 28 (15.9) 38 (14.4) 61 (13.8)
 3 16 (9.0) 5 (5.7) 15 (8.5) 20 (7.6) 36 (8.2)
 4 4 (2.3) 2 (2.3) 4 (2.3) 6 (2.3) 10 (2.3)
 5 3 (1.7) 2 (2.3) 1 (0.6) 3 (1.1) 6 (1.4)
 6 4 (2.3) 0 1 (0.6) 1 (0.4) 5 (1.1)
 7 3 (1.7) 0 1 (0.6) 1 (0.4) 4 (0.9)
 8 1 (0.6) 1 (1.1) 0 1 (0.4) 2 (0.5)

Data are presented as n (%)

CV cardiovascular

aDropout is only related to the recording of hospitalizations; there were no dropouts in the recording or follow-up on death