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Calcitonin gene-related peptide receptor or ligand (CGRP) antagonists for preventive treatment of migraine in adults

Calcitonin gene-related peptide receptor or ligand (CGRP) antagonists for preventive treatment of migraine in adults
Agent Dose (range) Maximum dose Notes
Parenteral monoclonal antibodies*
Erenumab 70 to 140 mg SUBQ once monthly 140 mg SUBQ once monthly
  • Auto-injector
Fremanezumab

225 mg SUBQ once monthly

-OR-

675 mg SUBQ once every 3 months

225 mg SUBQ once monthly

-OR-

675 mg SUBQ once every 3 months
  • Auto-injector
  • Dosing monthly or every 3-month interval
Galcanezumab 120 mg SUBQ once monthly (following initial 240 mg SUBQ loading dose) 120 mg SUBQ once monthly
  • Auto-injector
  • May also be used for cluster headache suppression (dosing regimen differs)
Eptinezumab 100 to 300 mg IV infusion once every 3 months 300 mg IV infusion once every 3 months
  • IV infusion over ≥30 minutes (in clinic)
  • Dosing every 3 months
Oral small molecule antagonists
Atogepant

Episodic migraine: 10 mg, 30 mg, or 60 mg orally once daily

Chronic migraine: 60 mg orally once daily
60 mg orally once daily
  • Dose adjustment required for kidney impairment
  • Significant drug interactions
Rimegepant Episodic migraine: 75 mg orally every other day 75 mg orally every other day
  • May also be used for acute migraine treatment (dosing regimen differs)
  • Orally disintegrating tablet
  • Dose adjustment required for kidney impairment
  • Significant drug interactions
CGRP antagonists may be effective preventive treatment for patients with marked disability from frequent migraines and/or those who do not respond to other preventive agents. Long-acting intravenous and subcutaneous formulations may be preferred by patients who have difficulty with daily preventive therapy. CRGP antagonists are avoided in patients with significant cardiovascular disease and pregnancy. Refer to UpToDate and Lexicomp drug monographs for full clinical use, precautions, and additional dosing details.

P-gp: P-glycoprotein drug efflux pump; CYP3A4: cytochrome p450 3A4 isoform; SUBQ: subcutaneous; IV: intravenous.

* Injection site reactions and constipation are most frequently reported adverse effects for parenteral agents.

¶ Small molecule "gepants" undergo CYP3A4 metabolism and are substrates of P-gp efflux pump. Specific interactions may warrant dose adjustment or avoidance of some combinations. To determine potential interactions for a specific patient's medication list, use the Lexicomp drug interactions program included within UpToDate.
Data from: Lexicomp Online (Lexi-Interact). Copyright © 1978-2024 Lexicomp, Inc. All Rights Reserved.
Graphic 141581 Version 5.0

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