UBRELVY is indicated for the acute treatment of migraine, with or without aura, in adults.
UBRELVY MECHANISM OF ACTION1*
UBRELVY MECHANISM OF ACTION1*
UBRELVY may relieve migraine by halting the cascade of CGRP-induced neurogenic inflammation, blocking CGRP-induced neurogenic vasodilation, and/or inhibiting the central relay of pain signals from the trigeminal nerve to the caudal trigeminal nucleus.1*
UBRELVY may relieve migraine by halting the cascade of CGRP-induced neurogenic inflammation, blocking CGRP-induced neurogenic vasodilation, and/or inhibiting the central relay of pain signals from the trigeminal nerve to the caudal trigeminal nucleus.1*
PHARMACOKINETICS*
UBRELVY is rapidly absorbed following oral administration with peak plasma concentrations observed around 1.5 hours post-dose.1
The elimination half-life of ubrogepant is approximately 5-7 hours.1
PHARMACOKINETICS*
UBRELVY is rapidly absorbed following oral administration with peak plasma concentrations observed around 1.5 hours post-dose.1
The elimination half-life of ubrogepant is approximately 5-7 hours.1
SAFETY INFORMATION
Click here for additional safety information and for a link to the Product Monograph discussing:
●Contraindications with concomitant use of strong CYP3A4 inhibitors.
●Relevant warnings and precautions regarding driving and operating machinery, hypersensitivity reactions, may reduce effectiveness of oral contraceptives, use in pregnant or breast-feeding women and dose selection in geriatric patients.
●Conditions of clinical use, adverse reactions, drug interactions and dosing instructions.
FOR MORE INFORMATION
For any questions related to UBRELVY, you can contact AbbVie Medical Information at 1-844-241-5011.
SAFETY INFORMATION
Click here for additional safety information and for a link to the Product Monograph discussing:
●Contraindications with concomitant use of strong CYP3A4 inhibitors.
●Relevant warnings and precautions regarding driving and operating machinery, hypersensitivity reactions, may reduce effectiveness of oral contraceptives, use in pregnant or breast-feeding women and dose selection in geriatric patients.
●Conditions of clinical use, adverse reactions, drug interactions and dosing instructions.
FOR MORE INFORMATION
For any questions related to UBRELVY, you can contact AbbVie Medical Information at 1-844-241-5011.
SAFETY INFORMATION
Click here for additional safety information and for a link to the Product Monograph discussing:
●Contraindications with concomitant use of strong CYP3A4 inhibitors.
●Relevant warnings and precautions regarding driving and operating machinery, hypersensitivity reactions, may reduce effectiveness of oral contraceptives, use in pregnant or breast-feeding women and dose selection in geriatric patients.
●Conditions of clinical use, adverse reactions, drug interactions and dosing instructions.
FOR MORE INFORMATION
For any questions related to UBRELVY, you can contact AbbVie Medical Information at
1-844-241-5011.
CGRP=calcitonin gene-related peptide.
* Clinical significance unknown.
† Comparative clinical significance unknown.
References:
1. UBRELVY (ubrogepant) Product Monograph. AbbVie Corporation.
2. Data on File, AbbVie Corporation.
3. “Summary Basis of Decision – Ubrelvy”. Health Canada. Updated March 30, 2023. https://hpr-rps.hres.ca/reg-content/summary-basis-decision-detailTwo.php?lang=en&linkID=SBD00631 (accessed April 19, 2023).
UBRELVY and its design are trademarks of Allergan Pharmaceuticals International Limited, an AbbVie company, used under license by AbbVie Corporation.
© 2024 AbbVie. All rights reserved.
CA-UBR-230004A / JN24
UBRELVY and its design are trademarks of Allergan Pharmaceuticals International Limited, an AbbVie company, used under license by AbbVie Corporation.
© 2024 AbbVie. All rights reserved.
CA-UBR-230004A / JN24