Eliquis Apizaban
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Prescribing Information

Risk Minimisation Material

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NVAF

Overview
Clinical Trial Aristotle
Clinical Trial Augustus
Real World Data

VTE-DVT / PE

Overview
Clinical Trial Amplify
Clinical Trial Amplify EXT
Real World Data

Dosing & Switching

Overview
Dosing in NVAF
Dosing in VTE-DVT / PE
Renal & Hepatic Impairment
Switching from and to Eliquis
Quick Reference Dosing Guide

Prescribers Checklist

Overview

Patient Resources

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Useful Links

Overview

Date of Preparation: January 2024 | Job Description: 432-IE-2300083

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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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