This brand name is authorized in United States. It is also authorized in Austria, Canada, Croatia, Cyprus, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Japan, Lithuania, New Zealand, Poland, Romania, Singapore, Spain, UK.
The drug AIMOVIG contains one active pharmaceutical ingredient (API):
1
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UNII
I5I8VB78VT - ERENUMAB
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Erenumab is a human monoclonal antibody that binds to the calcitonin gene-related peptide (CGRP) receptor. CGRP is a neuropeptide that modulates nociceptive signalling and a vasodilator that has been associated with migraine pathophysiology. Inhibition of the effects of CGRP could theoretically attenuate compensatory vasodilation in ischaemic-related conditions. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| AIMOVIG Solution for injection | MPI, EU: SmPC | European Medicines Agency (EU) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| N02CD01 | N Nervous system → N02 Analgesics → N02C Antimigraine preparations → N02CD Calcitonin gene-related peptide (CGRP) antagonists | |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| CA | Health Products and Food Branch | 02479613, 02487306 |
| EE | Ravimiamet | 1777091, 1777103, 1777114, 1794876, 1794887, 1794898 |
| ES | Centro de información online de medicamentos de la AEMPS | 1181293001, 1181293004 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 413894, 463750 |
| FR | Base de données publique des médicaments | 63401330, 64453981 |
| GB | Medicines & Healthcare Products Regulatory Agency | 357909, 375999 |
| HK | Department of Health Drug Office | 66406, 66847 |
| IE | Health Products Regulatory Authority | 89090, 89091 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 8285, 8449 |
| JP | 医薬品医療機器総合機構 | 1190406G1029 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1085963, 1085964, 1085965, 1087674, 1087675, 1087676 |
| NZ | Medicines and Medical Devices Safety Authority | 20339, 20694, 21964, 21965 |
| PL | Rejestru Produktów Leczniczych | 100409683, 100424435 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W64772001, W64773001, W64773002, W66104001 |
| SG | Health Sciences Authority | 15543P, 15545P |
| US | FDA, National Drug Code | 55513-840, 55513-841, 55513-842, 55513-843 |
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