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AboutInfliximabWhat is infliximabInflammatory Bowel DiseaseMaximising patient outcomes with IBDBiosimilarsWhat is a biosimilarFuture of biosimilarsBiologic switchingINFLECTRA® Introducing INFLECTRA® Position statementsECCOEULARESPGHANDosing & safetyDosingIV dosingAdministration & storageAdministrationStorageSafety informationImportant safety informationConsiderations for SwitchingSwitching to InflectraSafety informationImportant safety informationSafety informationSafety informationClinical evidenceRandomised controlled trial evidenceSummary: randomised controlled trial evidenceReal-world experienceSummary: real-world evidenceSupporting ResourcesVideosMaterialsPatient Support


Inflectra®(infliximab) Prescribing Information. Adverse events reporting information can be found at the bottom of the page.

 

IV dosing

Dosing with INFLECTRA® (CT-P13*/infliximab) is individualised based on each adult or paediatric patient’s weight, and can also be adjusted based on the clinical needs of each patient1,2

  • Including dose escalation or shortened dosing intervals to help regain or maintain clinical response in some patient populations1

Please refer to the INFLECTRA® SmPC for specific dosing recommendations

TitleINFLECTRA® is dosed identically to Remicade™†1,3

For full dosing information, access the INFLECTRA® Summary of Product Characteristics

CT-P13 is marketed under different brand names including INFLECTRA® and REMSIMA™.Remicade™ is a registered trademark of MSD.INFLECTRA® maintenance infusions are initiated on Dose 3 in patients with moderately to severely active Crohn’s disease. For all other indications, maintenance infusions are initiated on Dose 4.1INFLECTRA® maintenance infusions are given every 6-8 weeks in patients with ankylosing spondylitis. For all other indications, maintenance infusions are given every 8 weeks.1​​​​​​​IV, Intravenous.

Return to our Inflectra homepage to explore more about infliximab 

References:INFLECTRA® Summary of Product Characteristics.Schwartzman S, Morgan Jr, GJ. Arthritis Res Ther 2004;6:S19-23.Remicade™ Summary of Product Characteristics.
Dosing
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Learn switching information for INFLECTRA 
PP-IFA-GBR-0618. April 2023

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

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Adverse events should also be reported to Pfizer Medical Information on 01304 616161

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