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IV therapy with INFLECTRA® (CT-P13*/infliximab) provides an opportunity for qualified healthcare professionals to monitor treatment administration1,2
Please refer to the INFLECTRA® Summary of Product Characteristics and package leaflet for full administration instructions
For full administration information, access the INFLECTRA® Summary of Product Characteristics
View our 1 page PDF guide to support with the administration of the INFLECTRA® infusion
Learn about considerations when switching to INFLECTRA®
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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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PP-UNP-IRL-0176. January 2023