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Information relating to specific disease areas aligned to Pfizer’s portfolio and other resources designed for Pfizer medicines.

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For Inflectra® (infliximab) Prescribing Information for Great Britain click here.
Adverse event reporting information can be found at the bottom of the page.


NOR-SWITCH was a randomised, double-blind, non-inferiority parallel-group study that compared the effect of switching from Remicade® to Inflectra/CT-P13* (infliximab) in 481 patients across all indications.§1​​​​​​​

There was a similar adverse event profile in stable patients switching from Remicade® to CT-P13*, compared with those remaining on Remicade®.§

Treatment-emergent adverse events1

Safety population. Data are number of events/number of patients (%).
​​​​​​​Created from Jørgensen KK, et al. 2017.

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Rheumtaoid arthritis evidence

Learn about the safety and clinical evidence supporting the use of Inflectra in patient with rheumatoid arthritis

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Optimising treatment

Read the guidance on optimising treatment with Inflectra and TDM and biomarkers

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†Remicade® is a registered trademark of MSD.
*CT-P13 is marketed under different brand names including Inflectra and REMSIMA®.
§Only single one-way switching from Remicade® to CT-P13* was examined in this study. The NOR-SWITCH trial included only patients on Remicade® and CT-P13*; its findings do not support that any other biosimilars of infliximab can achieve the same result.
  1. Jørgensen KK, et al. Lancet 2017. 389:2304–2316.
PP-IFA-GBR-0499. September 2021

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  • PLANETRA safety

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  • PLANETAS efficacy

  • NOR-SWITCH safety

  • NOR-SWITCH effiacy

Learn about the evidence supporting the use of Inflectra in patients with Crohn’s disease. 

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For UK Healthcare Professionals*

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*The ABPI Code definition for healthcare professional is members of the medical, dental, pharmacy and nursing professionals and any other persons who in the course of their professional activities may administer, prescribe, purchase, recommend or supply a medicine.

PP-PFE-GBR-3863. November 2021



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