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Administration Video
This video will take you through the process of preparing and administering Vocabria + Rekambys
Dovato (dolutegravir/lamivudine) is available in Ireland for the treatment of HIV-1 in adults and adolescents above 12 years of age weighing at least 40kg, with no known or suspected resistance to the integrase inhibitor class, or lamivudine.1
DOVATO (dolutegravir/lamivudine)
Summary of product characteristics
Patient Information Leaflet
Vocabria ▼(cabotegravir) and Rekambys▼(rilpivirine) in combination are indicated for the treatment of HIV-1 infection in adults and adolescents (at least 12 years of age and weighing at least 35 kg), who are virologically suppressed (HIV-1RNA <50 copies/mL) on a stable antiretroviral regimen without present or past evidence of viral resistance to, and no prior virological failure with agents of the NNRTI and INI class.
VOCABRIA ▼ (cabotegravir) +
REKAMBYS ▼ (rilpivirine)
Abbreviated Prescribing Information
Vocabria Patient Information Leaflet
Rekambys Patient Information Leaflet
References
- Dovato Summary of Characteristics. Available at https://www.medicines.ie/medicines/dovato-50-mg-300-mg-film-coated-tablets-34871/spc. Last accessed: January 2025
- Vocabria Summary of Characteristics. Available at https://www.medicines.ie/medicines/vocabria-600-mg-prolonged-release-suspension-for-injection-35220/spc Last accessed: January 2025
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.
©2025 GSK group of companies. All rights reserved.
Date of Preparation: May 2025 PM-IE-HVX-WCNT-200003
