This website is for UK healthcare professionals and UK healthcare decision makers only

Reporting adverse events
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Some helpful resources and information on KAPRUVIA®arrow (difelikefalin) to
support your treatment goals for patients on in-centre HD with moderate
to severe chronic kidney disease-associated pruritus (CKD-aP)

KAPRUVIA® OVERVIEW

Download key information about CKD-aP and KAPRUVIA®, including efficacy, tolerability, mode of action and dosing

Download

KAPRUVIA® FORMULARY PACK

Download the formulary pack to help you with your applications for implementing KAPRUVIA® as a treatment

Download

KAPRUVIA® DOSING CARD

Find out how to dose and administer
KAPRUVIA® using this simple guide

Download

PATIENT IDENTIFICATION
LEAVEPIECE

Learn how to identify signs of moderate-to-severe CKD-aP and diagnose patients

Download

Kapruvia® Patient LEAFLET

Download the leaflet to help patients who have been prescribed KAPRUVIA® to learn more about the treatment

Download

CKD-aP, chronic kidney disease-associated pruritus; HD, haemodialysis.

Adverse events should be reported. Reporting forms and information can be found at https://yellowcard.mhra.gov.uk/ or search for MHRA Yellow Card in the Google Play or Apple App Store. Adverse events should also be reported to Vifor Pharma UK Ltd. (Tel 01276 853633). Email: medicalinfo_UK@viforpharma.com
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