What is the recommended daily dose of bempedoic acid for a patient with established cardiovascular disease (CVD) and elevated Low-Density Lipoprotein Cholesterol (LDL-C) despite maximally tolerated statin therapy?

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Last updated: January 7, 2026View editorial policy

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Recommended Daily Dose of Bempedoic Acid

The recommended daily dose of bempedoic acid is 180 mg taken orally once daily, with or without food. 1, 2, 3

Standard Dosing Protocol

  • Take 180 mg orally once daily as a single dose, which can be administered with or without food. 1, 2, 3

  • The tablet must be swallowed whole and should not be crushed or split. 2

  • No dose adjustment is required based on LDL-C response—the dose remains fixed at 180 mg daily regardless of lipid levels achieved. 2

Combination Therapy Dosing

  • When using the fixed-dose combination product with ezetimibe, take one tablet containing 180 mg bempedoic acid plus 10 mg ezetimibe once daily. 1, 2

  • If combining with bile acid sequestrants, administer bempedoic acid either 2 hours before or 4 hours after the bile acid sequestrant to avoid binding interactions. 2

Critical Dosing Restrictions with Statins

  • Do not exceed simvastatin 20 mg daily when used concomitantly with bempedoic acid due to increased statin exposure risk. 1, 2

  • Do not exceed pravastatin 40 mg daily when used concomitantly with bempedoic acid due to increased statin exposure risk. 1, 2

  • No dose restrictions apply when combining bempedoic acid with other statins (atorvastatin, rosuvastatin, etc.). 1

Special Population Considerations

  • No dosage adjustment is necessary in patients with mild or moderate hepatic impairment (Child-Pugh A or B). 3

  • Patients with severe hepatic impairment (Child-Pugh C) have not been studied, so use caution in this population. 3

  • No renal dose adjustment is required, though bempedoic acid exposure increases 1.5-fold in mild renal impairment, 2.3-fold in moderate impairment, and 2-fold in severe impairment. 3

Mandatory Safety Monitoring

  • Assess serum uric acid levels before initiating therapy and monitor if symptoms of hyperuricemia develop, as bempedoic acid increases uric acid by a mean of 0.8 mg/dL. 1, 2, 4

  • Monitor for signs and symptoms of tendinitis or tendon rupture; discontinue immediately if tendon rupture occurs. 1, 2

  • Monitor liver function tests as clinically indicated, particularly at baseline and periodically during treatment. 5, 2

Common Pitfalls to Avoid

  • Do not attempt to titrate the dose based on LDL-C response—180 mg daily is the only approved dose. 2

  • Do not combine with high-dose simvastatin (>20 mg) or pravastatin (>40 mg) as this significantly increases statin exposure and toxicity risk. 1, 2

  • Do not discontinue monitoring for hyperuricemia, as gout occurs in 1.5% of patients on bempedoic acid versus 0.4% on placebo. 6, 7

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Bempedoic Acid Dosing Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Role of Bempedoic Acid in Clinical Practice.

Cardiovascular drugs and therapy, 2021

Guideline

Intensifying Lipid-Lowering Therapy in High-Risk Patients

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Treatment of Hypercholesterolemia with Bempedoic Acid and Repatha

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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