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Safety and tolerability of etravirine
Enfermedades infecciosas y microbiología clínica, 2009-12, Vol.27 Suppl 2, p.21-26
2009
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Autor(en) / Beteiligte
Titel
Safety and tolerability of etravirine
Ist Teil von
  • Enfermedades infecciosas y microbiología clínica, 2009-12, Vol.27 Suppl 2, p.21-26
Ort / Verlag
Spain
Erscheinungsjahr
2009
Quelle
MEDLINE
Beschreibungen/Notizen
  • Etravirine (ETR) is the first representative of a new generation of non-nucleoside reverse transcriptase inhibitors (NNRTI) and is indicated in patients with HIV infection and virological failure. The recommended dose is 200 mg (two tablets) every 12 hours after a meal. ETR has good tolerability and the tablets can be dissolved in water, which can aid swallowing in some patients. This drug has a plasma half-life of 30-40 hours and consequently is a candidate for once-daily regimens. The most frequent adverse effect is rash (affecting 19% of patients), which is usually mild (grades 1 or 2) and does not lead to drug withdrawal. The DUET 1 and 2 studies, which compared ETR versus placebo, with both groups receiving boosted darunavir and an optimized background regimen, did not demonstrate a higher incidence of liver toxicity, neuropsychiatric symptoms, gastrointestinal disturbances or atherogenic dyslipidemia in patients receiving ETR. The safety profile of ETR suggests that it could be used as a substitute drug in patients with toxicity induced by first-generation NNRTIs or other antiretroviral drugs.

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