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Efficacy and SafetyClinical Efficacy RAORAL StrategyReal-World EvidenceORAL Surveillance and Integrated Safety SummaryClinical Efficacy PsAOPAL Clinical ProgrammeClinical Efficacy UCOCTAVE Study DesignOCTAVE Clinical ProgrammeSub GroupsPost-hoc AnalysesSafety and TolerabilitySafety Profile SummarySpecial Warnings & Precautions for UseAboutXELJANZ Mechanism of ActionDosing and AdministrationDosing in RA & PsADosingDosing in UCDosingSupport & ResourcesSupport & ResourcesMaterials
XELJANZ®: An oral JAK inhibitor approved for the treatment of RA, PsA, AS, UC and JIA1 Rheumatoid Arthritis

Find the information you need to support your RA patient here.

 Visit RA Efficacy Psoriatic Arthritis

Find the information you need to support your PsA patient here.

 Visit PsA Efficacy Ulcerative Colitis

Find the information you need to support your UC patient here.

 Visit UC Efficacy Treating With XELJANZ

If you are new to XELJANZ, learn more about XELJANZ dosing here.

 See recommended dosing for RA See recommended dosing for PsA See recommended dosing for UC Safety and Tolerability

Click here for an overview of the safety profile of XELJANZ.

 See XELJANZ safety data

Please refer to the XELJANZ Summary of Product Characteristics for full prescribing information

JAK=Janus kinase; RA=rheumatoid arthritis; UC=ulcerative colitis; PsA=psoriatic arthritis; AS=ankylosing spondylitis; JIA= juvenile idiopathic arthritis

References:XELJANZ Summary of Product Characteristics

Legal Category: S1A
Further information is available upon request

PP-XEL-IRL-0776 January 2023

Adverse events should be reported. Report an adverse event to your national reporting system (HPRA Pharmacovigilance)
 

Adverse events should also be reported to Pfizer Medical Information on 1800 633 363

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