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Explore our range of recorded webinars from international experts in the field of infectious disease.

A Three Chapter Webinar with Professor Guaraldi on The Art of Individualised Care: Making HIV a Smaller Part of Our Patients’ Lives

Dovato Abbreviated Prescribing Information

Chapter 1 of 3

Chapter 1: Frailty in HIV Patients

Chapter 2 of 3

Chapter 2: Ageing Healthy with HIV

Chapter 3 of 3

Chapter 3: Benefits of Patient Reported Outcomes (PROs)

POM A. Marketing Authorisation Number: EU/1/19/1370/001. Further information available from GlaxoSmithKline, 12 Riverwalk, Citywest, Business Campus, Dublin 24. Tel: 01-4955000.

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.

PM-IE-DLL-WCNT-240001 | Date of Preparation: March 2024

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.

▼ 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: March 2024 | PM-IE-HVX-WCNT-240001