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Table 1 (abstract P1). Treatment emergent adverse event and serious adverse event

From: Sepsis 2018

Patients with at least one

PlaceboN=12

0.3N=13

1.0N=12

3.0N=12

TotalN=49

TEAE

10 (83.3%)

12 (92.3%)

12 (100.0%)

11 (91.7%)

45 (91.8%)

Severe TEAE

8 (66.7%)

6 (46.2%)

5 (41.7%)

4 (33.3%)

23 (46.9%)

TEAE related to the study drug

2 (16.7%)

-

2 (16.7%)

-

4 (8.2%)

Serious AE incl. death

7 (58.3%)

4 (30.8%)

2 (16.7%)

4 (33.3%)

17 (34.7%)