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. 2020 Mar 4;24:74. doi: 10.1186/s13054-020-2792-z

Table 2.

Incidence of adverse events per treatment arm

IC43 100 μg (n = 393)No. (%) Placebo (n = 403)No. (%) P value Total (N = 796)No. (%)
Patients with ≥ 1 AE 366 (93.1) 389 (96.5) .0365 755 (94.8)
Most frequently reported AEs by preferred term (> 10%)a
 Diarrhea 57 (14.5) 52 (12.9) .5371 109 (13.7)
 Pyrexia 43 (10.9) 62 (15.4) .0747 105 (13.2)
 Urinary tract infection 53 (13.5) 52 (12.9) .8346 105 (13.2)
 Decubitus ulcer 53 (13.5) 49 (12.2) .5971 102 (12.8)
 Pneumonia 47 (12.0) 50 (12.4) .9138 97 (12.2)
Treatment-related AEs 27 (6.9) 23 (5.7) .5599 50 (6.3)
Severe AEs 236 (60.1) 235 (58.3) .6653 471 (59.2)
Treatment-related severe AEs 2 (0.5) 2 (0.5) 1.0000 4 (0.5)
Serious AEs 227 (57.8) 232 (57.6) 1.0000 459 (57.7)
Treatment-related serious AEs 0 (0.0) 1 (0.2) 1.0000 1 (0.1)
Medically attended AEs 347 (88.3) 356 (88.3) 1.0000 703 (88.3)
AEs occurring within 1 h after first vaccination 5 (1.3) 8 (2.0) .5783 13 (1.6)
AEs occurring within 1 h after second vaccination 3 (0.8) 3 (0.7) 1.0000 6 (0.8)

Abbreviation: AE adverse event

aPatients counted only once per preferred term (MedDRA 18.1). P values for pairwise comparisons: Fisher’s exact test