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

PROSIT-BIO SAE Summary

Safety

The primary endpoint was the the evaluation of safety in terms of rate of SAEs during the first year since the introduction of Inflectra/CT-P13* (infliximab) for the overall population.

Breakdown of SAEs experienced by the overall population.1

Adapted from Fliorino G. et al. 2017.

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Crohn’s disease safety

Learn about the safety profile of Inflectra in patients with Crohn’s disease

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Crohn’s disease dosing

Learn about the dosing and administration of Inflectra in patients with Crohn’s disease

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*CT-P13 is marketed under different brand names including Inflectra and REMSIMA®.
SAE=Serious adverse event
References
  1. Fiorino G, et al. Inflamm Bowel Dis 2017. 23:233–243.
PP-IFA-GBR-0503. September 2021

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  • GONCZI L et al

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  • Inflammatory bowel disease

Learn about the evidence supporting the use of Inflectra in patients with rheumatoid arthritis. 

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Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in Google Play or Apple App Store

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

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PP-PFE-GBR-2688. December 2020

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