Eliquis Apizaban
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This information is intended for healthcare professionals based in Ireland. If you are not a healthcare professional in Ireland, click here

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Prescribing Information

Risk Minimisation Material

Made in Irealand

HOME / ELIQUIS® (APIXABAN) DOSING INFORMATION ELIQUIS IRELAND / OVERVIEW

ELIQUIS® Dosing & Switching

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ELIQUIS Dosing for your adult patients with NVAF

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ELIQUIS Dosing for your adult patients with DVT / PE

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ELIQUIS dosing for your adult patients with renal and/or hepatic impairment

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Switching from and to ELIQUIS

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Quick Reference Dosing Guide

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Footnotes:

DVT = Deep Vein Thrombosis   NVAF = Non-Valvular Atrial Fibrillation   PE= Pulmonary Embolism

Date of Preparation: September 2025 | Job Description: 432-IE-2500027

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Reporting of suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via HPRA Pharmacovigilance at www.hpra.ie
Adverse reactions should also be reported to Bristol Myers Squibb Medical Information on 1 800 749 749 or medical.information@bms.com

Eliquis Apizaban

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