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Table 2: Distribution of serious and nonserious adverse events days 1–3 or 4 weeks after intrathecal gadobutrol, independent of dose (n = 196)a
iNPH Cohort Non-iNPH Cohort Days 1–3 4 Weeks Days 1–3 4 Weeks Serious adverse events Present (No.) 0 0 0 0 Absent (No.) (%) 144 (100%) 134 (100%) 52 (100%) 49 (100%) Nonserious adverse events Present (No.) (%) 47 (32.6%) 6 (4.5%) 30 (57.7%) 3 (6.1%) Absent (No.) (%) 97 (67.4%) 128 (95.5%) 22 (42.3%) 46 (93.9%) Missing data (No.) 0 10 0 3
a Data are presented as number of individuals (percentage are in parentheses). Comparison of the distribution of nonserious adverse events between the iNPH and non-iNPH cohorts after days 1–3 (Pearson χ2, P = .002) and 4 weeks (Pearson χ2, P = .649).