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This site is intended only for healthcare professionals resident in the United Kingdom

Eliquis (apixaban), an oral direct factor Xa inhibitor, is indicated for: prevention of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation (NVAF), with one or more risk factors, such as prior stroke or transient ischaemic attack (TIA); age ≥75 years; hypertension; diabetes mellitus; symptomatic heart failure (NYHA Class ≥II), treatment of deep vein thrombosis (DVT) and pulmonary embolism (PE), and prevention of recurrent DVT and PE in adults, prevention of venous thromboembolic events (VTE) in adult patients who have undergone elective hip or knee replacement surgery.

ELIQUIS® (apixaban)

Eliquis® Prescribing Information ► SUBSCRIBE to receive tailored information by email ►

 

Available to download in multiple languages at eliquis.co.uk
Available to download in multiple languages at eliquis.co.uk
Available to download in multiple languages at eliquis.co.uk
Click here to learn about switching to and from Eliquis® at eliquis.co.uk ►

 

Explore data in NVAF at eliquis.co.uk
Explore dosing and switching at eliquis.co.uk
Explore data in DVT / PE at eliquis.co.uk

BD = Twice Daily
DVT = Deep Vein Thrombosis
NVAF = Non-Valvular Atrial Fibrillation
PE = Pulmonary Embolism
SmPC = Summary of Product Characteristics
Reference: 1. Eliquis (apixaban) Summary of Product Characteristics
Eliquis® Prescribing Information

PP-ELI-GBR-6500. April 2020

Janrain Capture

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Copyright © 2016-2020 Pfizer Limited. All rights reserved.
This website is brought to you by Pfizer Limited, a company registered in England and Wales under No. 526209. Registered office: Ramsgate Road, Sandwich, Kent CT13 9NJ, VAT registration number GB201048427.
This site is intended only for healthcare professionals resident in the United Kingdom. If you are a member of the public wishing to access information on a specific medicine, please visit
www.medicines.org.uk/emc.

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 the Google Play or Apple App Store. Adverse events should also be reported to Pfizer Medical Information on 01304 616161.
PP-PFE-GBR-2464. April 2020

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These pages are not intended for patients or for members of the general public. The healthcare professional web pages contain promotional content.

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PP-GIP-GBR-3015 March 2018

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