Skip to main content

Table 4 Summary of treatment-emergent adverse events (regardless of causality) in either dosing subgroup

From: Sensitivity to angiotensin II dose in patients with vasodilatory shock: a prespecified analysis of the ATHOS-3 trial

 

Angiotensin II > 5 ng kg−1 min−1 (n = 84)

Angiotensin II ≤ 5 ng kg−1 min−1 (n = 79)

Any grade, n (%)

76 (90.5)

66 (83.5)

Grade 3/4, n (%)

64 (76.2)

43 (54.4)

Serious adverse events, n (%)

64 (76.2)

35 (44.3)

Adverse events resulting in discontinuation, n (%)

19 (22.6)

4 (5.1)

Fatal adverse events, n (%)

0

1 (1.3)