Abstract
Tenofovir disoproxil fumarate is a nucleotide analogue reverse transcriptase inhibitor approved by the FDA for the treatment of HIV infection. It is a potent agent with a long intracellular half-life that allows for once-daily dosing. It has been well tolerated in clinical trials, without evidence of the mitochondrial toxicity that has been associated with long-term treatment of some of the nucleoside analogue reverse transcriptase inhibitors. Because of its demonstrated efficacy and favourable safety profile, tenofovir disoproxil fumarate has quickly become a favoured nucleoside component of antiretroviral regimens for both treatment-naive and -experienced patients.
MeSH terms
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Adenine / administration & dosage
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Adenine / analogs & derivatives*
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Adenine / pharmacokinetics
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Adenine / therapeutic use
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Animals
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Drug Administration Schedule
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Drug Interactions
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Drug Resistance, Viral
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Drug Therapy, Combination
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HIV Infections / complications
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HIV Infections / drug therapy*
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Hepatitis B / complications
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Hepatitis B / drug therapy*
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Humans
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Organophosphonates / administration & dosage
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Organophosphonates / pharmacokinetics
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Organophosphonates / therapeutic use*
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Randomized Controlled Trials as Topic
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Reverse Transcriptase Inhibitors / administration & dosage
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Reverse Transcriptase Inhibitors / pharmacokinetics
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Reverse Transcriptase Inhibitors / therapeutic use*
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Tenofovir
Substances
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Organophosphonates
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Reverse Transcriptase Inhibitors
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Tenofovir
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Adenine