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1.
J Antimicrob Chemother ; 70(6): 1812-5, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25693997

RESUMO

OBJECTIVES: Boceprevir is a first-generation direct-acting antiviral licensed for the treatment of hepatitis C infection. Sildenafil is an oral therapy for erectile dysfunction. As boceprevir is a potent inhibitor of CYP3A4, potential pharmacokinetic interactions may occur when it is coadministered with sildenafil. The aim of this study was to assess the pharmacokinetic profile of sildenafil and boceprevir when dosed separately and together in healthy volunteers. METHODS: Thirteen male subjects completed the following study procedures: phase 1 (Day 0), a single dose of 25 mg of sildenafil was administered; washout period (Days 1-9); phase 2 (Days 10-15), 800 mg of boceprevir three times a day was administered; and phase 3 (Day 16), 800 mg of boceprevir and 25 mg of sildenafil were administered. All drugs were administered in the fed state. Intensive pharmacokinetic sampling was undertaken on Days 0, 15 and 16. Differences in the pharmacokinetic parameters of sildenafil, N-desmethyl-sildenafil and boceprevir between phase 3 and the earlier phases were evaluated by changes in the geometric mean ratios (GMRs). RESULTS: All the drugs were well tolerated with no safety concerns arising. In the presence of boceprevir (phase 3 versus phase 1), the GMR for the plasma Cmax and the AUC24 for sildenafil increased by 1.9-fold (95% CI 1.5-2.4) and 2.7-fold (95% CI 2.1-3.4), respectively, whereas a reduction in the Cmax of N-desmethyl-sildenafil was observed (GMR 0.5, 95% CI 0.4-0.7). No significant changes in boceprevir exposure were observed between phases 3 and 2. CONCLUSIONS: Exposure of sildenafil is increased in the presence of boceprevir. A dose adjustment of sildenafil is therefore necessary. An initial dose of 25 mg of sildenafil is suggested.


Assuntos
Antivirais/farmacocinética , Prolina/análogos & derivados , Citrato de Sildenafila/farmacocinética , Agentes Urológicos/farmacocinética , Adolescente , Adulto , Antivirais/administração & dosagem , Antivirais/efeitos adversos , Interações Medicamentosas , Voluntários Saudáveis , Humanos , Masculino , Pessoa de Meia-Idade , Plasma/química , Prolina/administração & dosagem , Prolina/efeitos adversos , Prolina/farmacocinética , Citrato de Sildenafila/administração & dosagem , Citrato de Sildenafila/efeitos adversos , Agentes Urológicos/administração & dosagem , Agentes Urológicos/efeitos adversos , Adulto Jovem
3.
Curr Opin Infect Dis ; 20(1): 47-53, 2007 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-17197881

RESUMO

PURPOSE OF REVIEW: The HIV virus has been present in our society for more than two decades. Although there was originally much academic interest in the possibility of prosecuting for the reckless transmission of HIV in England and Wales, it was thought impossible by many (including the government) under existing legislation. The first prosecution in England in 2003 (following the first UK prosecution in 2001, in Scotland) provoked a great deal of surprise not least in the HIV voluntary sector, which has since been campaigning for the cessation of such prosecutions. This review examines the law in this area and provides an understanding of the development of the ethical and other issues involved. RECENT FINDINGS: Since 2003 there have been seven further convictions for the reckless transmission of HIV in England and Wales. These prosecutions have led to several responses that are discussed here and the current developments in this area outlined. SUMMARY: Whether it is right to prosecute the reckless transmission of HIV remains a controversial, pressing question. This brief article aims to dissect and question the relevant issues and help inform this debate.


Assuntos
Direito Penal , Transmissão de Doença Infecciosa/legislação & jurisprudência , Infecções por HIV/psicologia , Infecções por HIV/transmissão , Política Pública , Parceiros Sexuais/psicologia , Inglaterra , Conhecimentos, Atitudes e Prática em Saúde , Humanos , Comportamento Sexual , País de Gales
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