You are now leaving GSK’s website

You are now leaving a GSK Website. By clicking this link, you will be taken to a website that is not owned or controlled by GSK, and GSK is not responsible for the content provided on that site.

Continue

Go back

Resources

  • Expand to See More

    NA

    V+R CROI VOLITION Poster

    Early Switch to CAB+RPV LA in Treatment-Naive Adults With HIV-1: Month 11 outcomes from VOLITION
    NP-IE-CBR-PSTR-260002

    DOWNLOAD NOW

    NA

    V+R CROI OPERA Poster

    Body Mass Index and Virologic Outcomes in Individuals on CAB+RPV LA in the OPERA Cohort
    NP-IE-CBR-PSTR-260001

    DOWNLOAD NOW

    NA

    V+R - VOLITION Infographic

    VOLITION Infographic summarising DoC and Outcomes Data at Month 11
    PM-IE-CBR-LBND-260002

    DOWNLOAD NOW

    nurse welcome booklet

    Nurse Welcome Booklet

    A guide to administering cabotegravir▼ + rilpivirine▼ long-acting injectables
    PM-IE-CBR-BKLT-250002

    DOWNLOAD NOW

     CROI 2025 Key Data Summary

    CROI 2025 Key Data Summary

    Summary deck looking at the OPERA 3 year availability data, OPERA women subgroup data and CARES 96 week data.
    PM-IE-CBR-PPT-250001

    DOWNLOAD NOW

Patient Resources

  • Expand to See More

    V&R Patient Information Leaflet

    Vocabria + Rekambys Patient Information Booklet

    A printed booklet to provide practical information for patients post-prescription of Vocabria + Rekambys. This is to support patients to understand the treatment and ensure people living with HIV are aware of their role in treatment success.
    NP-IE-CBR-LBND-230001

    ORDER NOW

Adverse events should be reported directly to the Health Products Regulatory Authority (HPRA) on their website: www.hpra.ie. Adverse events should also be reported to GlaxoSmithKline on 1800 244 255 or via online form https://gsk.public.reportum.com/.

These medicinal products are subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions.

REKAMBYS (rilpivirine long acting), including the trademark, is owned by the Janssen Pharmaceutical Companies and used under licence by the ViiV Healthcare group of companies.

All other trademarks are owned by the ViiV Healthcare group, or its licensor. 
©2026 GSK group of companies. All rights reserved.

Date of preparation: May 2026 | PM-IE-CBR-WCNT-240008