Healthcare Professionals should report suspected adverse reactions via their national reporting system.
Please provide as much information as possible when reporting suspected adverse reactions, including comorbidities, past medical history, concomitant medication, and relevant timings and dates.
If you have an adverse event to report for a UCB product, please follow the current regulatory procedure in your country or click on the following link to access the contact page of the UCB corporate website where you can report adverse events to UCB local affiliate contacts, UCB Cares or by completing the UCB AE webform.