Table 1.
References | Study Design | Number of Patients | Treatment | Rhabdomyolysis |
---|---|---|---|---|
Pedersen et al17 | RCT | 8888 | Simvastatin (20 mg/day) | 0.07% |
Atorvastatin (80 mg/day) | 0.05% | |||
Enger et al20 | RCT | 584,784 | Statin** | 0.003% |
Statin** + Fenofibrate* | 0.015% | |||
Statin** + Gemfibrozil* | 0.207% | |||
HPS2-THRIVE13 | RCT | 25,673 | Simvastatin (40 mg/day) + ER niacin (2 g/day) and laropiprant (40 mg/day) | 0.109% |
Simvastatin (40 mg/day) | 0.114% | |||
Cziraky et al21 | RCT | 473,343 | Atorvastatin* | 0.0057% |
Pravastatin* | 0.010% | |||
Simvastatin* | 0.0055% | |||
Lovastatin* | 0.0038% | |||
Fluvastatin* | 0.016% | |||
Rosuvastatin* | 0.012% | |||
Cerivastatin* | 0.085% | |||
Abraldes et al14 | RCT | 147 | Simvastatin (20 mg/day) (first 15 days) followed by simvastatin (40 mg/day) thereafter | 2.9% |
Giugliano et al11 | RCT | 15,281 | Simvastatin (40 mg) + ezetimibe (10 mg/day) | 0.137% |
Berwanger et al10 | RCT | 4191 | Loading doses of atorvastatin (80 mg/day), followed by atorvastatin (40 mg/day) | 0.142% |
Wierzbicki et al15 | Clinical Trial | 22 | Simvastatin (80 mg/day) | 0% |
Simvastatin (120 mg/day) | 4.5% | |||
Shepherd et al18 | Clinical Trial | 16,876 | Rosuvastatin (5–40 mg/day) | 0.047% |
Drobny et al19 | Clinical Trial | 198 | Rosuvastatin* | 3.03% |
Fluvastatin* | ||||
Goss et al12 | Clinical Trial phase 1 | 24 | Rosuvastatin (1–8 mg/kg/day) + erlotinib (150 mg/day) | 4.167% |
Pose et al16 | Clinical trial phase 2 | 50 | Simvastatin (40 mg/day) + rifaximin (1200 mg/day) | 19% |
Simvastatin (20 mg/day) + rifaximin (1200 mg/day) | 0% |
Notes: *Dose is not available; **Dose and type of drug are not available.
Abbreviation: RCT, randomized controlled trial.