Prophylaxis of migraine
Adult: In patients who have at least 4 migraine days per month: 70 mg once every 4 weeks, may increase to 140 mg every 4 weeks, if necessary. Consider treatment discontinuation if no response after 3 months.
Indications and Dosage
Subcutaneous
Prophylaxis of migraine Adult: In patients who have at least 4 migraine days per month: 70 mg once every 4 weeks, may increase to 140 mg every 4 weeks, if necessary. Consider treatment discontinuation if no response after 3 months.
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Special Precautions
Patient with hypertension or risk factors for hypertension, history of constipation, major CV or cerebrovascular events (e.g. pre-existing MI, stroke, TIA, unstable angina, undergone coronary artery bypass surgery or other revascularisation procedure). Elderly. Pregnancy and lactation.
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Adverse Reactions
Significant: Constipation, hypersensitivity reactions (e.g. rash, anaphylaxis, angioedema, swelling/oedema, urticaria), new-onset and worsening of pre-existing hypertension, immunogenicity.
General disorders and administration site conditions: Inj site reactions (e.g. pain, erythema). Musculoskeletal and connective tissue disorders: Muscle cramps or spasms. Skin and subcutaneous tissue disorders: Pruritus, rash. |
Monitoring Parameters
Monitor blood pressure. Monitor for signs and symptoms of hypersensitivity reactions and severe constipation.
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Drug Interactions
May increase the risk of severe constipation and constipation-related complications with drugs associated with reduced gastrointestinal motility.
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Action
Description:
Mechanism of Action: Erenumab is a human immunoglobulin G2 (IgG2) monoclonal antibody. It binds to and inhibits calcitonin gene-related peptide (CGRP), a peptide involved in migraine pathophysiology. Pharmacokinetics: Absorption: Bioavailability: 82%. Time to peak plasma concentration: Approx 6 days. Metabolism: Metabolised via nonspecific, nonsaturable proteolytic pathway. Excretion: Elimination half-life: 28 days. |
Storage
Store between 2-8°C. Protect from light. If removed from the refrigerator, store up to 30°C and use within 7 days. Do not freeze or shake.
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MIMS Class
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ATC Classification
N02CD01 - erenumab ; Belongs to the class of calcitonin gene-related peptide (CGRP) antagonists preparations. Used to relieve migraine.
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References
Aimovig 140 mg Solution for Injection in Pre-filled Pen (Novartis Pharmaceuticals UK Limited). MHRA. https://products.mhra.gov.uk. Accessed 06/11/2024. Aimovig Injection, Solution (Amgen Inc). DailyMed. Source: U.S. National Library of Medicine. https://dailymed.nlm.nih.gov/dailymed. Accessed 06/11/2024. Anon. Erenumab-aaoe. AHFS Clinical Drug Information [online]. Bethesda, MD. American Society of Health-System Pharmacists, Inc. https://www.ahfscdi.com. Accessed 06/11/2024. Brayfield A, Cadart C (eds). Erenumab. Martindale: The Complete Drug Reference [online]. London. Pharmaceutical Press. https://www.medicinescomplete.com. Accessed 06/11/2024. Erenumab. UpToDate Lexidrug, Lexi-Drugs Multinational Online. Waltham, MA. UpToDate, Inc. https://online.lexi.com. Accessed 06/11/2024. Joint Formulary Committee. Erenumab. British National Formulary [online]. London. BMJ Group and Pharmaceutical Press. https://www.medicinescomplete.com. Accessed 06/11/2024. Novartis New Zealand Limited. Aimovig 70 mg/mL, 140 mg/mL Solution for Injection in Pre-filled Pen and Syringe data sheet 6 March 2024. Medsafe. http://www.medsafe.govt.nz. Accessed 06/11/2024. Pasurta 140 mg/mL Solution for Injection in Prefilled Syringe (Novartis Corporation [Malaysia] Sdn. Bhd.). National Pharmaceutical Regulatory Agency - Ministry of Health Malaysia. https://www.npra.gov.my. Accessed 06/11/2024.
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