UBRELVY MECHANISM OF ACTION1*

UBRELVY MECHANISM OF ACTION1*

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 breastfeeding 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 breastfeeding 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 breastfeeding 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. 

© 2026 AbbVie. All rights reserved. 

CA-UBR-260029A / JN26  

UBRELVY and its design are trademarks of Allergan Pharmaceuticals International Limited, an AbbVie company, used under license by AbbVie Corporation. 

© 2026 AbbVie. All rights reserved. 

CA-UBR-260029A / JN26  

In vitro studies in coronary, meningeal and cerebral artery strips indicate that UBRELVY lacks vasoconstrictive effects in cranial and coronary arteries.1*

 

 

*  Clinical significance unknown. 

Reference:

1. UBRELVY (ubrogepant) Product Monograph. AbbVie Corporation. 

In vitro studies in coronary, meningeal and cerebral artery strips indicate that UBRELVY lacks vasoconstrictive effects in cranial and coronary arteries.1*

 

*  Clinical significance unknown. 

Reference:

1. UBRELVY (ubrogepant) Product Monograph. AbbVie Corporation.