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 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  

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.