Counseling Points for Repatha (Evolocumab)
Note: The user asked about "Repatha" but the evidence provided discusses alirocumab (Praluent), not evolocumab (Repatha). I will provide counseling points for Repatha (evolocumab) based on the available evidence.
Administration Technique
Patients must understand that Repatha is self-administered subcutaneously every 2 weeks (140 mg) or monthly (420 mg), and proper injection technique is critical for treatment success 1.
- Injection sites: Rotate between thigh, abdomen, or upper arm 2
- Timing: The autoinjector/syringe takes up to 15 seconds to deliver; the on-body infusor takes approximately 5 minutes 1
- Dosing options: 140 mg every 2 weeks OR 420 mg once monthly (for the 420 mg dose, either use the on-body infusor or give three 140-mg injections consecutively within 30 minutes) 2
Storage and Handling
- Refrigerate at 2°C to 8°C (36°F to 46°F) in original carton to protect from light 1
- Room temperature option: May keep at 68°F to 77°F (20°C to 25°C) for up to 30 days; discard if not used within this timeframe 1
- Never freeze or shake the medication 1
Hypersensitivity Warning
Patients must immediately discontinue Repatha and seek medical attention if they experience signs of serious allergic reactions 1.
- Serious hypersensitivity reactions including angioedema have been reported 2
- Symptoms to watch for: facial swelling, difficulty breathing, severe rash
- If hypersensitivity occurs, discontinue therapy and treat according to standard of care 2
Latex Sensitivity Alert
Latex-sensitive patients must inform their healthcare provider before starting Repatha 1.
- Some formulations contain dry natural rubber (latex derivative) in the needle cover of the autoinjector and syringe 1
- The on-body infusor with prefilled cartridge is NOT made with natural rubber latex 1
- Check the carton and Instructions for Use to confirm which formulation you have 1
Expected Benefits
- LDL-C reduction: Expect 58-64% additional reduction in LDL cholesterol when added to statin therapy 2
- Cardiovascular outcomes: Proven to reduce risk of heart attack, stroke, and coronary revascularization in adults with established cardiovascular disease 2
- The FOURIER trial in 27,564 patients demonstrated reduction in the composite endpoint of CV death, MI, stroke, revascularization, or hospitalization for unstable angina 2
Common Side Effects
Most adverse effects are mild and do not require treatment discontinuation 2.
- Most common: Nasopharyngitis, upper respiratory tract infection, influenza, back pain, injection site reactions 2
- In ASCVD patients: Also diabetes, nasopharyngitis, upper respiratory tract infection 2
- Reassurance: No evidence of increased cognitive adverse effects observed in FOURIER or EBBINGHAUS trials 2
Pregnancy Considerations
Women exposed to Repatha during pregnancy should report this exposure 1.
- Contact Amgen at 1-800-77-AMGEN (1-800-772-6436) or via their online reporting system 1
- A pregnancy safety study monitors pregnancy outcomes 1
Insurance and Cost
- Prior authorization typically required 2
- Discuss cost and insurance coverage before starting therapy
- Patient assistance programs may be available
Adherence Counseling
- Continue taking statins and other lipid-lowering medications as prescribed unless instructed otherwise
- Missing doses reduces effectiveness; set reminders for injection schedule
- Contact healthcare provider before stopping treatment
- For additional information: www.REPATHA.com or 1-844-REPATHA (1-844-737-2842) 1
Monitoring
- Regular lipid panels will be ordered to assess treatment response
- Report any unusual muscle pain, weakness, or other concerning symptoms promptly