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Review of tenofovir-emtricitabine

Highly active antiretroviral therapy has significantly reduced HIV-related morbidity and mortality. Increasingly, fixed-dose antiretroviral combinations with equal or greater potency than traditional antiretrovirals, along with fewer side effects, reduced toxicity, and simplified dosing convenience...

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Detalles Bibliográficos
Autores principales: Masho, Saba Woldemichael, Wang, Cun-Lin, Nixon, Daniel E
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2387297/
https://www.ncbi.nlm.nih.gov/pubmed/18516268
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author Masho, Saba Woldemichael
Wang, Cun-Lin
Nixon, Daniel E
author_facet Masho, Saba Woldemichael
Wang, Cun-Lin
Nixon, Daniel E
author_sort Masho, Saba Woldemichael
collection PubMed
description Highly active antiretroviral therapy has significantly reduced HIV-related morbidity and mortality. Increasingly, fixed-dose antiretroviral combinations with equal or greater potency than traditional antiretrovirals, along with fewer side effects, reduced toxicity, and simplified dosing convenience are being utilized. Tenofovir-emtricitabine (TDF-FTC) represents one of the more recent fixed-dose combinations. In combination with either a ritonavir-boosted protease inhibitor or a non-nucleoside reverse transcriptase inhibitor, TDF-FTC is a preferred choice in recent treatment guidelines on the basis of demonstrated potency in randomized clinical trials, one-pill-a-day dosing convenience, and relatively low toxicity. In addition, the drug is active against hepatitis B virus. Caution must be exercised in patients with renal insufficiency, or when the drug is used with certain other drugs. This manuscript reviews the use of TDF-FTC in the treatment of HIV.
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spelling pubmed-23872972008-05-30 Review of tenofovir-emtricitabine Masho, Saba Woldemichael Wang, Cun-Lin Nixon, Daniel E Ther Clin Risk Manag Review Highly active antiretroviral therapy has significantly reduced HIV-related morbidity and mortality. Increasingly, fixed-dose antiretroviral combinations with equal or greater potency than traditional antiretrovirals, along with fewer side effects, reduced toxicity, and simplified dosing convenience are being utilized. Tenofovir-emtricitabine (TDF-FTC) represents one of the more recent fixed-dose combinations. In combination with either a ritonavir-boosted protease inhibitor or a non-nucleoside reverse transcriptase inhibitor, TDF-FTC is a preferred choice in recent treatment guidelines on the basis of demonstrated potency in randomized clinical trials, one-pill-a-day dosing convenience, and relatively low toxicity. In addition, the drug is active against hepatitis B virus. Caution must be exercised in patients with renal insufficiency, or when the drug is used with certain other drugs. This manuscript reviews the use of TDF-FTC in the treatment of HIV. Dove Medical Press 2007-12 2007-12 /pmc/articles/PMC2387297/ /pubmed/18516268 Text en © 2007 Dove Medical Press Limited. All rights reserved
spellingShingle Review
Masho, Saba Woldemichael
Wang, Cun-Lin
Nixon, Daniel E
Review of tenofovir-emtricitabine
title Review of tenofovir-emtricitabine
title_full Review of tenofovir-emtricitabine
title_fullStr Review of tenofovir-emtricitabine
title_full_unstemmed Review of tenofovir-emtricitabine
title_short Review of tenofovir-emtricitabine
title_sort review of tenofovir-emtricitabine
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2387297/
https://www.ncbi.nlm.nih.gov/pubmed/18516268
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