Descovy (TAF/FTC)
Fixed-dose combination of tenofovir alafenamide 25 mg and emtricitabine 200 mg. Approved for HIV treatment and PrEP in men and transgender women who have sex with men (not studied in receptive vaginal exposure at approval). TAF component yields lower plasma tenofovir with improved renal and bone safety vs Truvada. One pill once daily with food.
Projected serum levels — 1 pill (≈ 225 mg), once daily
Maintenance schedule: 1 pill (≈ 225 mg) once daily (oral).
Modeled steady state after ~1 days: peak ≈ 85.1 mg, trough ≈ 4.4 mg body load. Population-based estimate over 15 days for a reference dose at a 70 kg reference body mass — the interactive app scales curves to your doses, timing, and body mass.
Key facts
- Category
- Antiretroviral
- Route modeled
- Oral
- Model confidence
- inferred
- Half-life
- 4.9 h
- Common dose
- 1 pill (≈ 225 mg)
- Suggested maximum
- 1 pill/day
- Reference dose range
- 0.50–1 pill (single dose)
- Suggested cadence
- once daily
Documented interactions
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watch
Biktarvy (BIC/FTC/TAF) + Descovy (TAF/FTC)
Biktarvy (BIC/FTC/TAF) and Descovy (TAF/FTC) both push the hiv reverse transcriptase nrti in the same direction.
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watch
Emtricitabine (FTC / Emtriva) + Descovy (TAF/FTC)
Descovy (TAF/FTC) and Emtricitabine (FTC / Emtriva) both push the hiv reverse transcriptase nrti in the same direction.
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watch
Lamivudine (3TC, Epivir) + Descovy (TAF/FTC)
Descovy (TAF/FTC) and Lamivudine (3TC, Epivir) both push the hiv reverse transcriptase nrti in the same direction.
Serum checks 4 modeled interaction pairings for descovy (taf/ftc) across your whole stack — absorption conflicts, enzyme inhibition, and nutrient depletion included.
Research behind this entry
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Emtricitabine and tenofovir alafenamide vs emtricitabine and tenofovir disoproxil fumarate for HIV pre-exposure prophylaxis (DISCOVER)
DISCOVER non-inferiority trial demonstrating F/TAF matched F/TDF for PrEP efficacy with improved renal and bone safety markers.
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Pharmacokinetics and safety of tenofovir alafenamide in HIV-uninfected subjects with severe renal impairment
PK study supporting TAF use without dose adjustment in moderate-to-severe renal impairment, a key differentiator from TDF.
2 published studies referenced in the app, each with a plain-language summary.