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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.

 

Maximising patient outcomes with IBDIn this video, Dr Nabil Quraishi, consultant gastroenterologist at University Hospitals Birmingham in the UK, discusses how to achieve the goal of ensuring good health through early, deep, and sustained remission for patients.

Click the play button below to watch Dr Quraishi explain how to maximise clinical outcomes for your patients with infliximab.
You can also find out which type of IBD patients might benefit most from treatment with infliximab.

For full administration and storage information, access the INFLECTRA® Summary of Product Characteristics

 

To learn about infliximab and switching information for INFLECTRA click the buttons below:

Introducing Inflectra

Infliximab is a cornerstone treatment for many inflammatory diseases – with more than 15 years of clinical experience across all indications.
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Considerations for Switching to Inflectra
The following considerations may be of use when switching to Inflectra 
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Return to our Inflectra homepage to explore more about Infliximab 

INFLECTRA® Summary of Product Characteristics.
PP-IFA-GBR-0641 May 2023
Infliximab
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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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