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Our Medicines
GSK × ViiV remains committed to developing and investing in new medicines and innovations that aim to improve the treatment success and quality of life of all people living with HIV.
DOVATO (dolutegravir/lamivudine)
DOVATO is indicated for the treatment of HIV-1 in adults and adolescents above 12 years weighing at least 40kg, with no known or suspected resistance to the integrase inhibitor class, or lamivudine.1
SUMMARY OF PRODUCT CHARACTERISTICS
VOCABRIA▼ (Cabotegravir) & REKAMBYS▼ (Rilpivirine)
Vocabria injection is indicated, in combination with rilpivirine injection, for the treatment of HIV-1 infection in adults 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.2,3
ABBREVIATED PRESCRIBING INFORMATION
REKAMBYS PATIENT INFORMATION LEAFLET
JULUCA (dolutegravir/rilpivirine)
JULUCA is indicated for the treatment of HIV-1 infection in adults who are virologically-suppressed on a stable ARV regimen for ≥6 months with no history of virological failure and no known or suspected resistance to any NNRTI or INI.4
SUMMARY OF PRODUCT CHARACTERISTICS
TRIUMEQ (dolutegravir/abacavir/
lamivudine)
Triumeq is indicated for the treatment of Human Immunodeficiency Virus (HIV) infected adults and adolescents above 12 years of age weighing at least 40 kg.5
Before initiating treatment with abacavir-containing products, screening for carriage of the HLA-B*5701 allele should be performed in any HIV-infected patient, irrespective of racial origin. Abacavir should not be used in patient known to carry the HLA-B*5701 allele.5
INFORMATION ON ABACAVIR HYPERSENSITIVITY REACTION
TIVICAY (dolutegravir)
Tivicay is indicated in combination with other anti-retroviral medicinal products for the treatment of Human Immunodeficiency Virus (HIV) infected adults, adolescents and children above 6 years of age.6
TIVICAY10/25/50MG SUMMARY OF PRODUCT CHARACTERISTICS
TIVICAY10/25/50MG PATIENT INFORMATION LEAFLET
References
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: February 2024 | PM-IE-HVX-WCNT-190009
