Updated
June 27, 2024
Reviewed
June 27, 2024

Nucleoside and Nucleotide Analogue Reverse Transcriptase Inhibitors (NRTIs)

Emtricitabine

Emtricitabine (FTC, Emtriva)
Formulations

Pediatric Oral Solution: 10 mg/mL

Capsule: 200 mg

Fixed-Dose Combination (FDC) Tablets

  • [Atripla and generic] Efavirenz 600 mg/emtricitabine 200 mg/tenofovir disoproxil fumarate 300 mg
  • [Biktarvy]
    • Bictegravir 50 mg/emtricitabine 200 mg/tenofovir alafenamide 25 mg
    • Bictegravir 30 mg/emtricitabine 120 mg/tenofovir alafenamide 15 mg
  • [Complera] Emtricitabine 200 mg/rilpivirine 25 mg/tenofovir disoproxil fumarate 300 mg
  • [Descovy]
    • Emtricitabine 200 mg/tenofovir alafenamide 25 mg
    • Emtricitabine 120 mg/tenofovir alafenamide 15 mg
  • [Genvoya] Elvitegravir 150 mg/cobicistat 150 mg/emtricitabine 200 mg/tenofovir alafenamide 10 mg
  • [Odefsey] Emtricitabine 200 mg/rilpivirine 25 mg/tenofovir alafenamide 25 mg
  • [Stribild] Elvitegravir 150 mg/cobicistat 150 mg/emtricitabine 200 mg/tenofovir disoproxil fumarate 300 mg
  • [Symtuza] Darunavir 800 mg/cobicistat 150 mg/emtricitabine 200 mg/tenofovir alafenamide 10 mg
  • [Truvada]
    • Emtricitabine 200 mg/tenofovir disoproxil fumarate 300 mg
    • Emtricitabine 167 mg/tenofovir disoproxil fumarate 250 mg
    • Emtricitabine 133 mg/tenofovir disoproxil fumarate 200 mg
    • Emtricitabine 100 mg/tenofovir disoproxil fumarate 150 mg

When using FDC tablets, refer to other sections of the Drug Appendix for information about the individual components of the FDC. See also Appendix A, Table 2. Antiretroviral Fixed-Dose Combination Tablets and Co-packaged Formulations: Minimum Body Weights and Considerations for Use in Children and Adolescents.

For additional information, see Drugs@FDA or DailyMed.

Dosing RecommendationsSelected Adverse Events

Neonatal and Infant (Aged 0 to <3 Months) Dose

Oral Solution

  • Emtricitabine (FTC) 3 mg/kg once daily

Child (Aged ≥3 Months) and Adolescent Dose

Oral Solution

  • FTC 6 mg/kg once daily (maximum 240 mg per dose). The maximum dose of oral solution is higher than the capsule dose, because a pediatric pharmacokinetic analysis reported that the plasma exposure for FTC was 20% lower in patients who received the oral solution than in patients who received the capsule formulation.

Capsules (For Patients Weighing >33 kg)

  • FTC 200 mg once daily

Adult Dose

Oral Solution for Patients Who Are Unable to Swallow Capsules

  • FTC 240 mg (24 mL) once daily

Capsules

  • FTC 200 mg once daily

[Atripla and Generic] Efavirenz/FTC/Tenofovir Disoproxil Fumarate (TDF)

Child and Adolescent (Weighing ≥40 kg) and Adult Dose

  • One tablet once daily
  • Take on an empty stomach.

[Biktarvy] Bictegravir/FTC/Tenofovir Alafenamide (TAF)

Neonate or Child (Aged <2 Years and Weighing <14 kg) Dose

  • No data are available on the appropriate dose of Biktarvy in children aged <2 years and weighing <14 kg. Studies are currently being conducted to identify the appropriate dose for this age and weight group.

Child, Adolescent, and Adult Dose

  • One tablet once daily, with or without food.
Body WeightDose
≥14 kg to <25 kgBictegravir 30 mg/emtricitabine 120 mg/‌tenofovir alafenamide 15 mg
≥25 kgBictegravir 50 mg/emtricitabine 200 mg/‌tenofovir alafenamide 25 mg
  • The U.S. Food and Drug Administration approved Biktarvy for use only in antiretroviral therapy (ART)-naive patients or to replace the current antiretroviral (ARV) regimen in patients who have been virologically suppressed (HIV RNA <50 copies/mL) on a stable ARV regimen with no history of treatment failure and no known mutations associated with resistance to the individual components of Biktarvy. Some members of the Panel on Antiretroviral Therapy and Medical Management of Children Living with HIV (the Panel) recommend the use of Biktarvy in patients with prior treatment failure and who have virus containing the M184V mutation.
  • See the Bictegravir section for additional information.

[Complera] FTC/Rilpivirine (RPV)/TDF

Child and Adolescent (Aged ≥12 Years and Weighing ≥35 kg) and Adult Dose

  • One tablet once daily in ART-naive patients who have baseline plasma HIV RNA ≤100,000 copies/mL. This dose of Complera also can be used to replace a stable ARV regimen in patients who are currently on their first or second regimen and who have been virologically suppressed (HIV RNA <50 copies/mL) with no history of treatment failure and no known mutations associated with resistance to the individual components of Complera.
  • Administer with a meal of at least 500 calories.

[Descovy] FTC/TAF

Child and Adolescent and Adult Dose

Body WeightDose
≥14 kg to <25 kgFTC 120 mg/TAF 15 mg, in combination with an integrase strand transfer inhibitor (INSTI) or a non-nucleoside reverse transcriptase inhibitor (NNRTI). In this weight band, Descovy should not be used with protease inhibitors (PIs) that require a cytochrome P450 (CYP) 3A inhibitor (e.g., ritonavir [RTV] or cobicistat [COBI]).
≥25 kg to <35 kgFTC 200 mg/TAF 25 mg, in combination with an INSTI or an NNRTI. In this weight band, Descovy should not be used with PIs that require a CYP3A inhibitor (i.e., RTV or COBI).
≥35 kgFTC 200 mg/TAF 25 mg, in combination with an INSTI, NNRTI, or boosted PI.

[Genvoya] Elvitegravir/Cobicistat (COBI)/FTC/TAF

Child and Adolescent (Weighing ≥25 kg) and Adult Dose

  • One tablet once daily with food in ART-naive patients. This dose of Genvoya also can be used to replace the current ARV regimen in patients who have been virologically suppressed (HIV RNA <50 copies/mL) on a stable ARV regimen with no history of treatment failure and no known mutations associated with resistance to the individual components of Genvoya.

[Odefsey] FTC/RPV/TAF

Child and Adolescent (Aged ≥12 Years and Weighing ≥35 kg) and Adult Dose

  • One tablet once daily in ART-naive patients with HIV RNA ≤100,000 copies per mL. This dose of Odefsey also can be used to replace the current ARV regimen in patients who have been virologically suppressed (HIV RNA <50 copies/mL) with no history of treatment failure and no known mutations associated with resistance to the individual components of Odefsey.
  • Administer with a meal of at least 500 calories.

[Stribild] Elvitegravir/COBI/FTC/TDF

Child and Adolescent (Weighing ≥35 kg with a Sexual Maturity Rating of 4 or 5) and Adult Dose

  • One tablet once daily with food in ART-naive patients. This dose of Stribild also can be used to replace the current ARV regimen in patients who have been virologically suppressed (HIV RNA <50 copies/mL) with no history of treatment failure and no known mutations associated with resistance to the individual components of Stribild.

[Symtuza] Darunavir (DRV)/COBI/FTC/TAF

Child and Adolescent (Weighing ≥40 kg) and Adult Dose

  • One tablet once daily with food in ART-naive patients or in patients who have been virologically suppressed (HIV RNA <50 copies/mL) with no known mutations associated with resistance to darunavir or tenofovir.

[Truvada] FTC/TDF 

Child, Adolescent, and Adult Dose

Truvada Dosing Table

Body WeightFTC/TDF Tablet
Once Daily
17 kg to <22 kgOne FTC 100 mg/TDF 150-mg tablet
22 kg to <28 kgOne FTC 133 mg/TDF 200-mg tablet
28 kg to <35 kgOne FTC 167 mg/TDF 250-mg tablet
≥35 kg and adultsOne FTC 200 mg/TDF 300-mg tablet
  • Hyperpigmentation/skin discoloration on palms and/or soles
Special Instructions
  • Although FTC can be administered without regard to food, some FDC tablet formulations that contain FTC have food requirements.
  • FTC oral solution can be kept at room temperature, up to 77°F (25°C), if used within 3 months; refrigerate oral solution for long-term storage.
  • Screen patients for hepatitis B virus (HBV) infection before using FTC or FDC tablets that contain FTC. Severe acute exacerbation of HBV infection can occur when FTC is discontinued; therefore, hepatic function and hepatitis B viral load should be monitored for several months after patients with HBV infection stop taking FTC.
Metabolism/Elimination
  • No CYP interactions
  • Eighty-six percent of FTC is excreted in urine. FTC may compete with other compounds that undergo renal elimination.

FTC Dosing in Patients with Hepatic Impairment

  • Atripla should be used with caution in patients with hepatic impairment.
  • Biktarvy, Genvoya, Stribild, and Symtuza are not recommended for use in patients with severe hepatic impairment.
  • Complera, Descovy, and Odefsey do not require dose adjustment in mild or moderate hepatic impairment, but should not be used in patients with severe hepatic impairment, because they have not been studied in this group.

FTC Dosing in Patients with Renal Impairment

  • Decrease the dose of FTC in patients with impaired renal function. Consult the manufacturer’s prescribing information for recommended dose adjustments.
  • Do not use the FDC tablets Atripla or Complera in patients with creatinine clearance (CrCl) <50 mL/min or in patients who require dialysis.
  • Do not use the FDC tablets Truvada or Biktarvy in patients with CrCl <30 mL/min. Do not use Truvada in patients who require dialysis.
  • Stribild should not be initiated in patients with estimated CrCl <70 mL/min and should be discontinued in patients with estimated CrCl <50 mL/min.
  • TAF-containing formulations are not recommended for use in patients with estimated CrCl <30 mL/min.

Drug Interactions

Additional information about drug interactions is available in the Adult and Adolescent Antiretroviral Guidelines and the HIV Drug Interaction Checker.

  • Other nucleoside reverse transcriptase inhibitors (NRTIs): Do not use emtricitabine (FTC) in combination with lamivudine (3TC), because these agents share similar resistance profiles and lack additive benefit. Do not use FTC with fixed-dose combination (FDC) medications that contain 3TC or FTC. See Appendix A, Table 1. Antiretrovirals Available in Fixed-Dose Combination Tablets or as a Co-packaged Formulation, by Drug Class, and refer to other sections of the Drug Appendix for drug interaction information for each individual component of an FDC tablet.
  • Renal elimination: FTC may compete with other compounds that undergo renal tubular secretion. Drugs that decrease renal function could decrease clearance of FTC.

Major Toxicities

  • More common: Headache, insomnia, diarrhea, nausea, rash. Hyperpigmentation/skin discoloration, which may be more common in children than in adults.
  • Less common (more severe): Neutropenia. Lactic acidosis and severe hepatomegaly with steatosis, including fatal cases, have been reported. Exacerbations of hepatitis have occurred in patients with hepatitis B virus (HBV)/HIV coinfection who switched from regimens that included FTC to regimens that did not include FTC.

Resistance

The International Antiviral Society–USA maintains a list of HIV drug resistance mutations, and the Stanford University HIV Drug Resistance Database offers a discussion of each mutation.

Pediatric Use

Approval

FTC is approved by the U.S. Food and Drug Administration for once-daily administration in children, starting at birth. FTC often is used as part of a dual-NRTI backbone in antiretroviral (ARV) regimens for children and adolescents because of its once-daily dosing, minimal toxicity, and favorable pediatric pharmacokinetic (PK) data.

Efficacy and Pharmacokinetics

Comparative Clinical Trials

Studies that assess the efficacy and/or potency of nucleoside/nucleotide analogues have been more concerned with the dynamic components of the regimen—such as tenofovir disoproxil fumarate (TDF), tenofovir alafenamide (TAF), or abacavir—than the more static components, such as FTC or 3TC. FTC and 3TC have been considered interchangeable, but data to support this conclusion are lacking. Investigators studying the AIDS Therapy Evaluation in the Netherlands (ATHENA) cohort compared the efficacy of TDF plus FTC with TDF plus 3TC when these drugs were administered with a ritonavir-boosted protease inhibitor (darunavir, atazanavir, or lopinavir) in antiretroviral therapy (ART)-naive patients.1 The adjusted hazard ratio for the virologic failure of 3TC-containing regimens compared with FTC-containing regimens within 240 weeks of starting therapy was 1.15 (95% confidence interval, 0.58–2.27). No difference between these regimens was observed in the time to virologic suppression during the first 48 weeks of therapy or time to virologic failure after attaining suppression. A Swiss cohort study found a potential difference in efficacy between FTC and 3TC; however, the difference disappeared after adjusting for pill burden.2 Current evidence suggests that FTC and 3TC have equivalent efficacy and toxicity in ARV-naive patients.

Efficacy

Following a dose-finding study (described in the Pharmacokinetics: Liquid Versus Capsule section below),3 a once-daily dose of FTC 6 mg/kg administered in combination with other ARV drugs was studied in 116 patients aged 3 months to 16 years.4 The study used a maximum dose of 240 mg of the FTC liquid formulation. PK results showed that the plasma exposures seen in these children and adolescents were similar to those seen in adults who received FTC 200 mg once daily. Follow-up data extending to Week 96 indicated that 89% of ART-naive children and 76% of ARV-experienced children maintained plasma HIV RNA <400 copies/mL (75% of ARV-naive children and 67% of ARV-experienced children had HIV RNA <50 copies/mL). Minimal toxicity was observed during this trial. Pediatric AIDS Clinical Trials Group (PACTG) P10215 evaluated the use of FTC 6 mg/kg (with a maximum dose of FTC 200 mg per day of the liquid formulation) as part of a three-drug regimen dosed once daily to ARV-naive children aged 3 months to 21 years. In this trial, 85% of children achieved HIV RNA <400 copies/mL, and 72% of children maintained virologic suppression (HIV RNA <50 copies/mL) through 96 weeks of therapy. The median CD4 T lymphocyte count rose by 329 cells/mm3 at Week 96.

Pharmacokinetics: Liquid Versus Capsule

A single-dose PK study of the FTC oral solution and FTC capsules enrolled 25 children with HIV aged 2 years to 17 years.3 FTC was found to be well absorbed following oral administration, with a mean elimination half-life of 11 hours (range, 9.7–11.6 hours). Plasma concentrations in children who received the once-daily dose of FTC 6 mg/kg were approximately equivalent to those seen in adults who received the standard dose of FTC 200 mg. However, plasma concentrations of FTC after administration of the capsule formulation were approximately 20% higher than those observed after administration of the oral solution in this small cohort of children.

Pharmacokinetics in Infants

A study in South Africa evaluated the PKs of FTC in 20 infants aged <3 months with perinatal HIV exposure. The participants received a dose of FTC 3 mg/kg once daily for two 4-day courses, separated by an interval of ≥2 weeks.6 FTC exposure (area under the curve [AUC]) in neonates receiving FTC 3 mg/kg once daily was within the range of exposures seen in pediatric patients aged >3 months who received the recommended dose of FTC 6 mg/kg once daily and adults who received the recommended dose of FTC 200 mg once daily. During the first 3 months of life, FTC AUC decreased with increasing age, correlating with an increase in total body clearance of the drug. In a small group of neonates (n = 6) who received a single dose of FTC 3 mg/kg and whose mothers received a single dose of FTC 600 mg during delivery, the FTC AUC exceeded the AUC seen in adults and older children. However, FTC had a half-life of 9.2 hours in these neonates, which is similar to that observed in adults and older children.7 Extensive safety data are lacking for this age range.

Considerations for Use

The FTC oral solution has an advantage over the liquid formulation of 3TC because it can be given once daily at ARV initiation, whereas the liquid formulation of 3TC needs to be given twice daily at ARV initiation. When pill formulations of 3TC or FTC are used, they can be administered once daily.

Both FTC and 3TC have antiviral activity and efficacy against HBV. For a comprehensive review of this topic, see the Hepatitis B Virus section in the Pediatric Opportunistic Infection Guidelines.

References

  1. Rokx C, Gras L, van de Vijver D, et al. Virological responses to lamivudine or emtricitabine when combined with tenofovir and a protease inhibitor in treatment-naive HIV-1-infected patients in the Dutch AIDS Therapy Evaluation in the Netherlands (ATHENA) cohort. HIV Med. 2016;17(8):571-580 Available at: http://www.ncbi.nlm.nih.gov/pubmed/26842457.
  2. Yang WL, Kouyos RD, Scherrer AU, et al. Assessing efficacy of different nucleos(t)ide backbones in NNRTI-containing regimens in the Swiss HIV cohort study. J Antimicrob Chemother. 2015;70(12):3323-3331. Available at: http://www.ncbi.nlm.nih.gov/pubmed/26362944.
  3. Wang LH, Wiznia AA, Rathore MH, et al. Pharmacokinetics and safety of single oral doses of emtricitabine in human immunodeficiency virus-infected children. Antimicrob Agents Chemother. 2004;48(1):183-191. Available at: http://www.ncbi.nlm.nih.gov/pubmed/14693538.
  4. Saez-Llorens X, Violari A, Ndiweni D, et al. Long-term safety and efficacy results of once-daily emtricitabine-based highly active antiretroviral therapy regimens in human immunodeficiency virus-infected pediatric subjects. Pediatrics. 2008;121(4):e827-835. Available at: http://www.ncbi.nlm.nih.gov/pubmed/18332076.
  5. McKinney RE, Jr., Rodman J, Hu C, et al. Long-term safety and efficacy of a once-daily regimen of emtricitabine, didanosine, and efavirenz in HIV-infected, therapy-naive children and adolescents: Pediatric AIDS clinical trials group protocol P1021. Pediatrics. 2007;120(2):e416-423. Available at: http://www.ncbi.nlm.nih.gov/pubmed/17646352.
  6. Blum M, Ndiweni D, Chittick Gea. Steady state pharmacokinetic evaluation of emtricitabine in neonates exposed to HIV in utero. Presented at: Conference on Retroviruses and Opportunistic Infections; 2006. Denver, CO. Available at.
  7. Flynn PM, Mirochnick M, Shapiro DE, et al. Pharmacokinetics and safety of single-dose tenofovir disoproxil fumarate and emtricitabine in HIV-1-infected pregnant women and their infants. Antimicrob Agents Chemother. 2011;55(12):5914-5922. Available at: http://www.ncbi.nlm.nih.gov/pubmed/21896911.

Nucleoside and Nucleotide Analogue Reverse Transcriptase Inhibitors (NRTIs)

Emtricitabine

Emtricitabine (FTC, Emtriva)
Formulations

Pediatric Oral Solution: 10 mg/mL

Capsule: 200 mg

Fixed-Dose Combination (FDC) Tablets

  • [Atripla and generic] Efavirenz 600 mg/emtricitabine 200 mg/tenofovir disoproxil fumarate 300 mg
  • [Biktarvy]
    • Bictegravir 50 mg/emtricitabine 200 mg/tenofovir alafenamide 25 mg
    • Bictegravir 30 mg/emtricitabine 120 mg/tenofovir alafenamide 15 mg
  • [Complera] Emtricitabine 200 mg/rilpivirine 25 mg/tenofovir disoproxil fumarate 300 mg
  • [Descovy]
    • Emtricitabine 200 mg/tenofovir alafenamide 25 mg
    • Emtricitabine 120 mg/tenofovir alafenamide 15 mg
  • [Genvoya] Elvitegravir 150 mg/cobicistat 150 mg/emtricitabine 200 mg/tenofovir alafenamide 10 mg
  • [Odefsey] Emtricitabine 200 mg/rilpivirine 25 mg/tenofovir alafenamide 25 mg
  • [Stribild] Elvitegravir 150 mg/cobicistat 150 mg/emtricitabine 200 mg/tenofovir disoproxil fumarate 300 mg
  • [Symtuza] Darunavir 800 mg/cobicistat 150 mg/emtricitabine 200 mg/tenofovir alafenamide 10 mg
  • [Truvada]
    • Emtricitabine 200 mg/tenofovir disoproxil fumarate 300 mg
    • Emtricitabine 167 mg/tenofovir disoproxil fumarate 250 mg
    • Emtricitabine 133 mg/tenofovir disoproxil fumarate 200 mg
    • Emtricitabine 100 mg/tenofovir disoproxil fumarate 150 mg

When using FDC tablets, refer to other sections of the Drug Appendix for information about the individual components of the FDC. See also Appendix A, Table 2. Antiretroviral Fixed-Dose Combination Tablets and Co-packaged Formulations: Minimum Body Weights and Considerations for Use in Children and Adolescents.

For additional information, see Drugs@FDA or DailyMed.

Dosing RecommendationsSelected Adverse Events

Neonatal and Infant (Aged 0 to <3 Months) Dose

Oral Solution

  • Emtricitabine (FTC) 3 mg/kg once daily

Child (Aged ≥3 Months) and Adolescent Dose

Oral Solution

  • FTC 6 mg/kg once daily (maximum 240 mg per dose). The maximum dose of oral solution is higher than the capsule dose, because a pediatric pharmacokinetic analysis reported that the plasma exposure for FTC was 20% lower in patients who received the oral solution than in patients who received the capsule formulation.

Capsules (For Patients Weighing >33 kg)

  • FTC 200 mg once daily

Adult Dose

Oral Solution for Patients Who Are Unable to Swallow Capsules

  • FTC 240 mg (24 mL) once daily

Capsules

  • FTC 200 mg once daily

[Atripla and Generic] Efavirenz/FTC/Tenofovir Disoproxil Fumarate (TDF)

Child and Adolescent (Weighing ≥40 kg) and Adult Dose

  • One tablet once daily
  • Take on an empty stomach.

[Biktarvy] Bictegravir/FTC/Tenofovir Alafenamide (TAF)

Neonate or Child (Aged <2 Years and Weighing <14 kg) Dose

  • No data are available on the appropriate dose of Biktarvy in children aged <2 years and weighing <14 kg. Studies are currently being conducted to identify the appropriate dose for this age and weight group.

Child, Adolescent, and Adult Dose

  • One tablet once daily, with or without food.
Body WeightDose
≥14 kg to <25 kgBictegravir 30 mg/emtricitabine 120 mg/‌tenofovir alafenamide 15 mg
≥25 kgBictegravir 50 mg/emtricitabine 200 mg/‌tenofovir alafenamide 25 mg
  • The U.S. Food and Drug Administration approved Biktarvy for use only in antiretroviral therapy (ART)-naive patients or to replace the current antiretroviral (ARV) regimen in patients who have been virologically suppressed (HIV RNA <50 copies/mL) on a stable ARV regimen with no history of treatment failure and no known mutations associated with resistance to the individual components of Biktarvy. Some members of the Panel on Antiretroviral Therapy and Medical Management of Children Living with HIV (the Panel) recommend the use of Biktarvy in patients with prior treatment failure and who have virus containing the M184V mutation.
  • See the Bictegravir section for additional information.

[Complera] FTC/Rilpivirine (RPV)/TDF

Child and Adolescent (Aged ≥12 Years and Weighing ≥35 kg) and Adult Dose

  • One tablet once daily in ART-naive patients who have baseline plasma HIV RNA ≤100,000 copies/mL. This dose of Complera also can be used to replace a stable ARV regimen in patients who are currently on their first or second regimen and who have been virologically suppressed (HIV RNA <50 copies/mL) with no history of treatment failure and no known mutations associated with resistance to the individual components of Complera.
  • Administer with a meal of at least 500 calories.

[Descovy] FTC/TAF

Child and Adolescent and Adult Dose

Body WeightDose
≥14 kg to <25 kgFTC 120 mg/TAF 15 mg, in combination with an integrase strand transfer inhibitor (INSTI) or a non-nucleoside reverse transcriptase inhibitor (NNRTI). In this weight band, Descovy should not be used with protease inhibitors (PIs) that require a cytochrome P450 (CYP) 3A inhibitor (e.g., ritonavir [RTV] or cobicistat [COBI]).
≥25 kg to <35 kgFTC 200 mg/TAF 25 mg, in combination with an INSTI or an NNRTI. In this weight band, Descovy should not be used with PIs that require a CYP3A inhibitor (i.e., RTV or COBI).
≥35 kgFTC 200 mg/TAF 25 mg, in combination with an INSTI, NNRTI, or boosted PI.

[Genvoya] Elvitegravir/Cobicistat (COBI)/FTC/TAF

Child and Adolescent (Weighing ≥25 kg) and Adult Dose

  • One tablet once daily with food in ART-naive patients. This dose of Genvoya also can be used to replace the current ARV regimen in patients who have been virologically suppressed (HIV RNA <50 copies/mL) on a stable ARV regimen with no history of treatment failure and no known mutations associated with resistance to the individual components of Genvoya.

[Odefsey] FTC/RPV/TAF

Child and Adolescent (Aged ≥12 Years and Weighing ≥35 kg) and Adult Dose

  • One tablet once daily in ART-naive patients with HIV RNA ≤100,000 copies per mL. This dose of Odefsey also can be used to replace the current ARV regimen in patients who have been virologically suppressed (HIV RNA <50 copies/mL) with no history of treatment failure and no known mutations associated with resistance to the individual components of Odefsey.
  • Administer with a meal of at least 500 calories.

[Stribild] Elvitegravir/COBI/FTC/TDF

Child and Adolescent (Weighing ≥35 kg with a Sexual Maturity Rating of 4 or 5) and Adult Dose

  • One tablet once daily with food in ART-naive patients. This dose of Stribild also can be used to replace the current ARV regimen in patients who have been virologically suppressed (HIV RNA <50 copies/mL) with no history of treatment failure and no known mutations associated with resistance to the individual components of Stribild.

[Symtuza] Darunavir (DRV)/COBI/FTC/TAF

Child and Adolescent (Weighing ≥40 kg) and Adult Dose

  • One tablet once daily with food in ART-naive patients or in patients who have been virologically suppressed (HIV RNA <50 copies/mL) with no known mutations associated with resistance to darunavir or tenofovir.

[Truvada] FTC/TDF 

Child, Adolescent, and Adult Dose

Truvada Dosing Table

Body WeightFTC/TDF Tablet
Once Daily
17 kg to <22 kgOne FTC 100 mg/TDF 150-mg tablet
22 kg to <28 kgOne FTC 133 mg/TDF 200-mg tablet
28 kg to <35 kgOne FTC 167 mg/TDF 250-mg tablet
≥35 kg and adultsOne FTC 200 mg/TDF 300-mg tablet
  • Hyperpigmentation/skin discoloration on palms and/or soles
Special Instructions
  • Although FTC can be administered without regard to food, some FDC tablet formulations that contain FTC have food requirements.
  • FTC oral solution can be kept at room temperature, up to 77°F (25°C), if used within 3 months; refrigerate oral solution for long-term storage.
  • Screen patients for hepatitis B virus (HBV) infection before using FTC or FDC tablets that contain FTC. Severe acute exacerbation of HBV infection can occur when FTC is discontinued; therefore, hepatic function and hepatitis B viral load should be monitored for several months after patients with HBV infection stop taking FTC.
Metabolism/Elimination
  • No CYP interactions
  • Eighty-six percent of FTC is excreted in urine. FTC may compete with other compounds that undergo renal elimination.

FTC Dosing in Patients with Hepatic Impairment

  • Atripla should be used with caution in patients with hepatic impairment.
  • Biktarvy, Genvoya, Stribild, and Symtuza are not recommended for use in patients with severe hepatic impairment.
  • Complera, Descovy, and Odefsey do not require dose adjustment in mild or moderate hepatic impairment, but should not be used in patients with severe hepatic impairment, because they have not been studied in this group.

FTC Dosing in Patients with Renal Impairment

  • Decrease the dose of FTC in patients with impaired renal function. Consult the manufacturer’s prescribing information for recommended dose adjustments.
  • Do not use the FDC tablets Atripla or Complera in patients with creatinine clearance (CrCl) <50 mL/min or in patients who require dialysis.
  • Do not use the FDC tablets Truvada or Biktarvy in patients with CrCl <30 mL/min. Do not use Truvada in patients who require dialysis.
  • Stribild should not be initiated in patients with estimated CrCl <70 mL/min and should be discontinued in patients with estimated CrCl <50 mL/min.
  • TAF-containing formulations are not recommended for use in patients with estimated CrCl <30 mL/min.

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