ORAL Strategy Safety Outcomes
  • AE rates, including rates of the most common AEs, were comparable between treatment arms.1
  • The majority of AEs were mild or moderate in severity.1
Adapted from Fleischmann R et al. 2017.1

Safety analysis set was identical to the full analysis set. Two (1%) of patients receiving XELJANZ monotherapy died during the first year of therapy.1

*Patients could have experienced more than one AE.1
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Safety & Tolerability
Please click here for an overview of the safety profile of XELJANZ across all licensed indications.
AE, adverse event; BID, twice-daily; MTX, methotrexate; Q2W, once every 2 weeks; SAE, serious adverse event. ​​​​​​​
1. Fleischmann R et al. Lancet 2017; 390:457–468.
PP-XEL-GBR-3116. August 2021
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.

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