Skip to main content
. 2014 Jul 12;14:53. doi: 10.1186/1471-2253-14-53

Table 3.

Adverse events (AEs) occurring for ≥ 5% subjects in any treatment group, regardless of relation to study drug (all-subjects-treated group)

 
Chinese
Caucasian
  Sugammadex (n = 120) Neostigmine (n = 111) Sugammadex (n = 29) Neostigmine (n = 31)
Subjects with any AE (n, %)
84 (70)
91 (82)
20 (69)
26 (84)
Abdominal pain
1 (1)
6 (5)
1 (3)
1 (3)
Upper abdominal pain
6 (5)
2 (2)

2 (6)
Nausea
10 (8)
13 (12)
4 (14)
7 (23)
Odynophagia
6 (5)
3 (3)


Vomiting
11 (9)
11 (10)


Fatigue


2 (7)

Pyrexia
16 (13)
16 (14)
2 (7)
1 (3)
Sensation of foreign body
7 (6)
4 (4)


Cardiac anesthetic complication
1 (1)
6 (5)

4 (13)
Incision site pain
28 (23)
26 (23)


Procedural hypotension



5 (16)
Procedural nausea
4 (3)
7 (6)


Procedural pain
10 (8)
10 (9)
13 (45)
12 (39)
Procedural vomiting
4 (3)
7 (6)


Wound complication
3 (3)
2 (2)
3 (10)
3 (10)
Dizziness
11 (9)
21 (19)
2 (7)

Headache
5 (4)
6 (5)
1 (3)
1 (3)
Insomnia
2 (2)
1 (1)
2 (7)
2 (6)
Vaginal hemorrhage
5 (4)
9 (8)


Increased upper airway secretion 5 (4) 10 (9)