Rosuvastatin Dosing for Hypercholesterolemia and Cardiovascular Risk
For most adult patients with hypercholesterolemia or cardiovascular disease risk, initiate rosuvastatin at 10-20 mg once daily, with the dose range extending from 5-40 mg depending on LDL-C goals, cardiovascular risk stratification, renal function, ethnicity, and drug interactions. 1, 2
Standard Dosing by Indication
High-Intensity Therapy (≥50% LDL-C Reduction)
- Rosuvastatin 20-40 mg daily is classified as high-intensity statin therapy for patients with established ASCVD (acute coronary syndromes, MI, stable/unstable angina, coronary revascularization, stroke, TIA, or peripheral arterial disease) who are ≤75 years old 1
- Patients with LDL-C ≥190 mg/dL should receive high-intensity rosuvastatin (20-40 mg) regardless of other risk factors 1
- Very high-risk patients with multiple major risk factors, diabetes, severe uncontrolled risk factors, or metabolic syndrome benefit from intensive LDL lowering to <70 mg/dL using rosuvastatin 20-40 mg 1
Moderate-Intensity Therapy (30-49% LDL-C Reduction)
- Rosuvastatin 5-10 mg daily achieves moderate-intensity LDL-C reduction for primary prevention in adults aged 40-75 years based on cardiovascular risk assessment 1
- Patients >75 years with ASCVD should receive moderate-intensity therapy (5-10 mg) as there is no clear evidence of additional ASCVD event reduction from high-intensity therapy in this age group 1
Pediatric Dosing
- Ages 8 to <10 years with HeFH: 5-10 mg once daily 2
- Ages ≥10 years with HeFH: 5-20 mg once daily 2
- Ages ≥7 years with HoFH: 20 mg once daily 2
Critical Dose Modifications
Severe Renal Impairment (CrCl <30 mL/min/1.73 m²)
- Start at 5 mg once daily and do not exceed 10 mg daily in patients not on hemodialysis 3, 1, 2
- No dose adjustment needed for mild to moderate renal impairment 3
Asian Patients
- Initiate at 5 mg once daily due to significantly higher rosuvastatin plasma concentrations compared to white patients 1, 2
- Consider risks and benefits when treating Asian patients not adequately controlled at doses up to 20 mg once daily 2
Drug Interaction Dose Limits
- Cyclosporine, tacrolimus, everolimus, or sirolimus: Do not exceed 5 mg daily (7-fold increase in rosuvastatin exposure with severe muscle toxicity risk) 1, 2
- Teriflunomide, enasidenib, capmatinib: Do not exceed 10 mg daily 2
- Gemfibrozil: Avoid concomitant use; if necessary, initiate at 5 mg and do not exceed 10 mg daily 2
- Fostamatinib, febuxostat: Do not exceed 20 mg daily 2
- Resmetirom (for MASH/NASH): Limit rosuvastatin to 20 mg daily 1
- Protease inhibitors (atazanavir/ritonavir, lopinavir/ritonavir): Initiate at 5 mg and do not exceed 10 mg daily 2
- Darolutamide: Do not exceed 5 mg daily 2
Administration and Monitoring
Practical Administration
- Administer once daily at any time of day, with or without food 2
- Swallow tablets whole 2
- When taking with aluminum/magnesium hydroxide antacids, administer rosuvastatin at least 2 hours before the antacid 2
Monitoring Timeline
- Assess LDL-C as early as 4 weeks after initiating therapy and adjust dosage if necessary 2
- For statin conversions, monitor lipid levels 4-12 weeks after conversion to ensure equivalent efficacy 4
Comparative Efficacy Data
LDL-C Reduction by Dose
- Rosuvastatin 5 mg: 42-45% LDL-C reduction 5, 6
- Rosuvastatin 10 mg: 52% LDL-C reduction 5
- Rosuvastatin 20 mg: Approximately 55-60% LDL-C reduction 5
- Rosuvastatin 40 mg: 63% LDL-C reduction 5
Superior to Other Statins
- Rosuvastatin 10 mg produces significantly greater LDL-C reduction than atorvastatin 10 mg, simvastatin 20 mg, or pravastatin 40 mg 1, 5
- Rosuvastatin 5 mg is significantly more effective than atorvastatin 10 mg (42% vs 36% LDL-C reduction, P<0.001), simvastatin 20 mg (42% vs 36%, P<0.001), and pravastatin 20 mg (42% vs 27%, P<0.001) 6
Common Pitfalls to Avoid
- Do not automatically start all patients at 10 mg without considering ethnicity and renal function—Asian patients and those with severe renal impairment require the lower 5 mg starting dose to avoid excessive drug exposure and increased myopathy risk 1
- Do not exceed dose limits when prescribing with interacting medications, particularly cyclosporine (5 mg maximum) 1, 2
- Do not use simvastatin 80 mg as an alternative due to increased myopathy risk 7
- Verify the patient is not on hemodialysis before applying the severe renal impairment dosing restrictions 2