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Tenofovir Disoproxil Fumarate: There were insufficient numbers from racial and ethnic groups other than Caucasian to adequately determine potential pharmacokinetic differences among these populations following the administration of tenofovir DF.

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Comparison of amphotericin B with fluconazole in the treatment of acute AIDS-associated cryptococcal meningitis.

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Nineteen antiretroviral drugs have been approved for the treatment of HIV-1 infection: one nucleotide and seven nucleoside reverse transcriptase inhibitors (NRTIs), seven protease inhibitors (PIs), three nonnucleoside RT inhibitors (NNRTIs), and one fusion inhibitor.

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The prognosis for most persons with IRIS is favorable because a robust inflammatory response may predict an excellent response to HAART in terms of immune reconstitution and, perhaps, improved survival.

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Think of PrEP as an HIV prevention option where HIV-negative individuals take a pill to prevent HIV infection for the “season” when they are most at risk for being exposed to HIV.

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In one embodiment of the present invention, the esterification of Tenofovir monohydrate is carried out in the presence of a base and Wittig reagent, wherein base is selected from organic amine like trialkyl amine such as triethylamine, diisopropyl ethyl amine preferably triethylamine and the wittig reagent is selected from the group comprising Isopropyl triphenylphosphonium iodide, triphenylphosphonium bromide, n-propyl triphenyl phosphonium bromide, -propyl triphenyl phosphonium iodide, ethyl triphenylphosphonium iodide, ethyl triphenylphosphonium bromide, tert-butyl triphenylphosphonium iodide, tert-butyl triphenylphosphonium bromide.

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The goal of HAART is to reduce the amount of virus in your body, or the viral load, to a level that can no longer be detected with blood tests.

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