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HCV or antiretroviral therapy, as the safety of increased tenofovir concentrations in this setting has not been established.

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After about 2 weeks of starting the medication regularly, severe breakouts occurred.

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Although prevention and new medical interventions may reduce the pace of the epidemic, HIV will be a significant disease for many years both in the United States and the world.

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Gilead Sciences donated the study medication but had no role in data collection, data analysis, or manuscript preparation.

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as the researchers found more toxicity on the combivir arm than on the truvada arm

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Strengthening HIV surveillance in the antiretroviral therapy era: rationale and design of a longitudinal study to monitor HIV prevalence and incidence in the uMgungundlovu District, KwaZulu-Natal, South Africa.

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At the hearing the FDA stressed that regular adherence counseling will be essential with PrEP.

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The researchers also conducted a small study to determine the blood concentrations of tenofovir diphosphate that resulted from taking a Truvada pill 2, 4 and 7 days per week.

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Stakeholder Engagement in HIV Cure Research: Lessons Learned from Other HIV Interventions and the Way Forward.

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Accumulated data from animal and human clinical and observational studies demonstrate that ART initiated as soon as possible within 48 to 72 hours of sexual, injection-drug use, and other substantial nonoccupational HIV exposure and continued for 28 days might reduce the likelihood of transmission.

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