Information on how to access XELJANZ®▼ (tofacitinib citrate) prescribing information and adverse event reporting can be found at the bottom of the page.
Always refer to the full Prescribing Information before prescribing XELJANZ.
Tablets shown not true to size.
Note: the dose should not be exceeded
Watch Professor Ernest Choy's lecture on understanding the clinical significance of JAK selectivity in RA
* XELJANZ contains lactose. Patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption should not take this medicinal product.
MTX - methotrexate; BID - twice daily; QD - once daily; TB - tuberculosis; RA - rheumatoid arthritis; PsA - psoriatic arthritis.
XELJANZ Risk Minimisation Programme (RMP) materials, including a Patient Alert Card, Prescriber Checklists and a Prescriber Brochure are available from https://www.medicines.org.uk/emc/. Patients treated with XELJANZ should be given the Patient Alert Card.
These pages are not intended for patients or for members of the general public. The healthcare professional web pages contain promotional content.
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PP-PFE-GBR-3863. November 2021
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