Table 4.
Adverse events during hospitalisation according to study groups
Adverse event | Simvastatin n=19 |
Placebo n=15 |
p Value |
---|---|---|---|
AST level, median (IQR), (ukat/L) | 0.25 (0.22–0.36) | 0.7 (0.3–0.94) | 0.08 |
AST>2 times upper reference limit | 1 (5.2%) | 3 (20%) | 0.30 |
ALT level, median (IQR), (ukat/L) | 0.28 (0.22–0.43) | 0.68 (0.3–1.0) | 0.19 |
ALT>2 times upper reference limit | 2 (10.5%) | 2 (13.3%) | 1 |
CK level, median (IQR), (ukat/L) | 0.87 (0.51–2.22) | 0.60 (0.32–2.7) | 0.53 |
CK>2 times upper reference limit | 1 (5.2%) | 1 (6.6%) | 1 |
ALT, alanine aminotransferase; AST, aspartate aminotransferase; CK, creatine kinase.