Viread DF was approved in 2001 as an antiretroviral drug (ARV) for people with HIV infection. In US treatment guidelines, Viread is listed as a preferred drug for people just starting ART. Viread nephrotoxicity is characterized by proximal tubular cell dysfunction that may be associated with acute kidney injury or chronic kidney disease. Withdrawal of the drug leads to improvement of analytical parameters that may be partial. Understanding the risk factors for nephrotoxicity and regular monitoring of proximal tubular dysfunction and serum creatinine in high-risk patients is required to minimize nephrotoxicity.
Other names for this medication:
Tenofovir,
Atripla,
Tenvir,
Trioday,
Truvada,
Viraday,
Viread,
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