Aimovig

Active Ingredient(s): Erenumab-aooe
FDA Approved: * May 17, 2018
Pharm Company: * AMGEN INC
Category: Migraine / Tension Headache

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".



Aimovig Overview

Erenumab, sold under the brand name Aimovig, is a medication which targets the calcitonin gene-related peptide receptor (CGRPR) for the prevention of migraine.[2][3][4] Erenumab was approved in May 2018 and was the first of a group of four CGRPR antagonists to be approved by the U.S. Food and Drug Administration (FDA) that year. It is a form of monoclonal antibody therapy in which antibodies are used to block the receptors for the protein CGRP,...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Erenumab

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Possible Dosages for this and Related Drugs:

Erenumab-aooe
  • Injection: 70mg/ml
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Aimovig: (4 results)

Sorted by National Drug Code
  • 55513-840 Aimovig 70 mg/ml Subcutaneous Injection by Amgen Inc
  • 55513-841 Aimovig 70 mg/ml Subcutaneous Injection by Amgen Inc
  • 55513-842 Aimovig 140 mg/ml Subcutaneous Injection, Solution by Amgen Inc
  • 55513-843 Aimovig 140 mg/ml Subcutaneous Injection, Solution by Amgen Inc

Other drugs which contain Erenumab-aooe or a similar ingredient: (1 result)