Can a patient take a 420 mg dose of Repatha (evolocumab) orally?

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Last updated: February 21, 2026View editorial policy

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Can a Patient Take 420 mg of Repatha?

Yes, 420 mg is a standard FDA-approved dose of Repatha (evolocumab), but it must be administered subcutaneously—never orally—either once monthly or every 2 weeks depending on the indication. 1

Route of Administration: Critical Safety Point

  • Repatha cannot be taken by mouth. It is a monoclonal antibody that would be destroyed by digestive enzymes if swallowed and must be given as a subcutaneous injection. 1
  • The 420 mg dose is administered subcutaneously using either three consecutive 140 mg injections within 30 minutes at different sites, or via a prefilled single-dose on-body infusor. 2
  • Approved injection sites include the thigh, abdomen, or upper arm, with rotation of sites recommended. 2

Standard 420 mg Dosing Regimens

For adults with ASCVD, primary hyperlipidemia, or heterozygous familial hypercholesterolemia (HeFH):

  • 420 mg subcutaneously once monthly is equivalent in efficacy to 140 mg every 2 weeks. 2, 1
  • The once-monthly 420 mg regimen reduces LDL-C by approximately 58%, while the every-2-week 140 mg regimen reduces it by 64%—both are clinically comparable. 2
  • Choice between regimens can be based on patient preference without compromising efficacy. 3

For pediatric patients ≥10 years with HeFH:

  • The same dosing applies: either 140 mg every 2 weeks or 420 mg once monthly. 2, 1

Higher-Intensity 420 mg Dosing

For homozygous familial hypercholesterolemia (HoFH):

  • Initial dose is 420 mg once monthly. 2, 1
  • If inadequate LDL-C reduction after 12 weeks, the dose can be escalated to 420 mg every 2 weeks (effectively doubling the monthly dose). 2, 1
  • Patients on lipid apheresis may start directly with 420 mg every 2 weeks to align with their apheresis schedule, administered after each session. 1

Administration Preparation

  • Allow refrigerated Repatha to warm to room temperature for at least 30 minutes (autoinjector or syringe) or 45 minutes (on-body infusor) before injection. 1
  • Visually inspect the solution—it should be clear to opalescent, colorless to pale yellow; do not use if cloudy, discolored, or contains particles. 1
  • Some presentations contain dry natural rubber (latex derivative) in the needle cover; prescribe latex-free presentations for latex-sensitive patients. 2, 1

Efficacy of the 420 mg Dose

  • When added to maximally tolerated statin therapy, the 420 mg monthly dose achieves a median LDL-C of 30 mg/dL (59% reduction from baseline median of 92 mg/dL). 3, 4
  • In the FOURIER trial, 86% of participants used the every-2-week regimen, but both schedules demonstrated cardiovascular benefit with a 15% reduction in major adverse cardiovascular events. 3, 4
  • The 420 mg dose also reduces non-HDL-C by 51%, lipoprotein(a) by 27%, and triglycerides by 16%. 3

Common Pitfall to Avoid

  • Never attempt oral administration. Patients or caregivers unfamiliar with biologic therapies may mistakenly believe any medication can be swallowed. Emphasize that Repatha is a subcutaneous injection only and provide hands-on training per the Instructions for Use. 1
  • When monitoring LDL-C in patients on the 420 mg monthly regimen, measure just prior to the next scheduled dose, as LDL-C can vary during the dosing interval. 1

References

Guideline

Repatha (Evolocumab) Dosing Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Evolocumab (PCSK9 Inhibitor) for LDL‑C Reduction and Cardiovascular Risk Management in High‑Risk ASCVD Patients

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

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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