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Resources
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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
Viral Blips and Low-level Viremia Pooled Analysis
A digital leave behind to help address concerns around viral blips for patients on Vocabria + Rekambys
PM-IE-CBR-LBND-250001
2024 AIDS Abstract Booklet
A digital booklet containing three abstracts from AIDS 2024, focusing on the CARLOS, BEYOND and COMBINE-2 Studies.
PM-IE-CBR-BKLT-240001
Patient Resources
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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
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.
©2024 GSK group of companies. All rights reserved.
Date of preparation: May 2025 | PM-IE-CBR-WCNT-240008
