Skip to main content
. 2016 Jul 2;20:206. doi: 10.1186/s13054-016-1386-2

Table 2.

Summary of adverse events observed during the study

Adverse event Dexmedetomidine (n = 16) Propofol (n = 10) Total (n = 26)
Subjects, n (%) Events, n Subjects, n (%) Events, n Subjects, n (%) Events, n
Bradycardia 1 (6.3) 1 1 (3.8) 1
Cardiac arrest 1 (10.0) 1 1 (3.8) 1
Urinary tract infection 1 (6.3) 1 1 (3.8) 1
Decreased cough efficiency 1 (10.0) 1 1 (3.8) 1
Increased bronchial secretion 1 (10.0) 1 1 (3.8) 1