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Table 4 Adverse events and serious adverse events

From: A multi-center, randomized, double-blind, parallel, placebo-controlled trial to evaluate the efficacy, safety, and pharmacokinetics of intravenous ibuprofen for the treatment of fever in critically ill and non-critically ill adults

Number of subjects (% of treatment group)

100 mg IV Ibuprofen

200 mg IV Ibuprofen

400 mg IV Ibuprofen

Placebo

Subjects experiencing no AEs

4

13%

5

17%

8

26%

3

11%

Subjects experiencing any AEs (including SAEs)

27

87%

25

83%

23

74%

25

89%

Subjects experiencing SAEs (including death)

6

19%

5

17%

4

13%

4

14%

Patient deaths

1

3%

2

7%

2

6%

1

4%

Total subjects

31

 

30

 

31

 

28