United Kingdom (incl. Northern Ireland): Healthcare Professionals are asked to report any suspected adverse reactions via Yellow Card Scheme found at https://yellowcard.mhra.gov.uk/.
Ireland: Healthcare Professionals are asked to report any suspected adverse reactions via HPRA at www.HPRA.ie.
All adverse events (UK and Ireland) should also be reported to BeiGene at adverse_events@beigene.com; (UK: 08009176799; Ireland: 1800812061).
For medical information, please contact: UK: 08004320266, Ireland: 1800946589 or email: medicalinformationEU@beigene.com
▼ This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information.
October 2023 [1023-BRU-PRC-054]
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Brukinsa®▼ UK and Ireland healthcare professional website
This website contains information on BRUKINSA (zanubrutinib) and is intended for healthcare professionals in the UK and Ireland only.
To direct you to the most appropriate information, please confirm you are a UK or Ireland Healthcare Professional.
If you are not a UK or Ireland Healthcare Professional, you will be directed to the BRUKINSA Patient Information leaflet.
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0823-BRU-PRC-184 | September 2023
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