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. 2016 Jul 26;9(6):823–835. doi: 10.1177/1756283X16658252

Table 5.

Total number of adverse events with grading and presentation time in treated (ornithine phenylacetate) and placebo patients.

Severity Infusion
(70)
Follow up
(53)
Total
(123)
Placebo
n (%)
OP
n (%)
Placebo
n (%)
OP
n (%)
Placebo
n (%)
OP
n (%)
40 (100%) 30 (100%) 28 (100%) 25 (100%) 68 (100%) 55 (100%)
Mild 29 (72.5%) 21 (70%) 22 (78.5%) 12 (48%) 51 (72.8%) 33 (55.9%)
Moderate 9 (22.5%) 8 (26.6%) 4 (14.2%) 8 (32%) 13 (18.5%) 16 (27.1%)
Severe 2 (5%) 1 (3.3%) 2 (7.1%) 5 (20%) 4 (5.7%) 6 (10.1%)

OP, ornithyne phenylactetate.