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▼This medicine (AQUIPTA®) is subject to additional monitoring. This will allow quick identification of new safety information.

AQUIPTA® is contraindicated in patients with hypersensitivity to the active substance or to any of the excipients.1,2 AQUIPTA® is not recommended during pregnancy. A decision must be made whether to discontinue breastfeeding or to discontinue AQUIPTA® therapy taking into account the benefit of breastfeeding for the child and benefit of therapy for the woman.1,2

Please consult the full Summary of Product Characteristics.

CGRP, calcitonin gene-related protein

Reference:

1. AQUIPTA® UK Summary of Product Characteristics. Available at: https://www.medicines.org.uk/emc/product/15049/smpc. Accessed November 2023

2. AQUIPTA® (atogepant) EU Summary of Product Characteristics. August 2023. Available at: https://www.ema.europa.eu/en/medicines/human/EPAR/aquipta. Accessed November 2023

Reference:

1. AQUIPTA® UK Summary of Product Characteristics. Available at: https://www.medicines.org.uk. Accessed November 2023

2. AQUIPTA® (atogepant) EU Summary of Product Characteristics. August 2023. Available at: https://www.ema.europa.eu. Accessed November 2023

UK-NEUR-230022 | Date of preparation: November 2023.

Adverse events should be reported. Reporting forms and information can be found at yellowcard.mhra.gov.uk.

Adverse events should also be reported to AbbVie on [email protected]