Body
Drug(s) | Usual Dose | Dosage Adjustment in Renal Insufficiency | ||
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CrCl (mL/min)* | Dose | |||
Acyclovir | IV Dose Serious HSV:
|
26–50 | 100% of dose IV every 12 hours | |
10–25 | 100% of dose IV every 24 hours | |||
<10 | 50% of dose IV every 24 hours | |||
HD | 50% of dose every 24 hours; administer dose after HD on day of dialysis. | |||
PO Dose for Herpes Zoster: 800 mg PO five times/day | 10–25 | 800 mg PO every 8 hours | ||
<10 | 800 mg PO every 12 hours | |||
HD | 800 mg PO every 12 hours; administer dose after HD on day of dialysis | |||
Adefovir | 10 mg PO every 24 hours | 30–49 | 10 mg PO every 48 hours | |
10–29 | 10 mg PO every 72 hours | |||
HD | 10 mg PO weekly; administer dose after HD | |||
Amikacin For mycobacterial infections |
IV 15 mg/kg per day or 25 mg/kg three times per week |
Use with caution in patients with renal insufficiency and family history of ototoxicity. | Adjust dose based on serum concentrations with target peak concentration 35–45 mcg/mL and trough concentration <4 mcg/mL. Administer dose after HD on day of dialysis. |
|
Amphotericin B | 0.7–1.0 mg/kg IV per day (amphotericin B deoxycholate) or 3–6 mg/kg IV per day (lipid formulation) |
N/A | No dosage adjustment necessary; consider alternative antifungals if renal insufficiency occurs during therapy despite adequate hydration. | |
Capreomycin | 15 mg/kg IV or IM per day | Use with caution in patients with renal insufficiency. | Adjust dose based on serum concentrations with target peak concentration 35–45 mcg/mL and trough concentration <4 mcg/mL. Administer dose after HD on day of dialysis. |
|
Chloroquine (Base) |
For Treatment of Acute Malaria:
|
<10 | 50% of dose | |
Cidofovir | 5 mg/kg IV on Day 0, repeat 5 mg/kg IV dose on Day 7, then 5 mg/kg IV every 2 weeks Give each dose with probenecid and saline hydration (see Table 2 for dosing instructions). |
Pretreatment SCr >1.5 mg/dL or CrCl <55 mL/min or Proteinuria ≥100 mg/dL (≥2 +) |
Cidofovir is not recommended. | |
If SCr increases by 0.3–0.4 mg/dL above baseline | Decrease to 3 mg/kg IV per dose | |||
If SCr increases >0.5 mg/dL above baseline |
Discontinue therapy | |||
Ciprofloxacin | 500–750 mg PO every 12 hours or 400 mg IV every 8–12 hours |
30–50 | 500–750 mg PO every 12 hours or 400 mg IV every 12 hours |
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<30 | 250–500 mg PO every 24 hours or 400 mg IV every 24 hours |
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HD or PD | 250–500 mg PO every 24 hours or 200–400 mg IV every 24 hours; administer after HD or PD on day of dialysis. |
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Clarithromycin | 500 mg PO every 12 hours | 30–60 | Usual dose except when used with an HIV PI or with COBI, then reduce dose by 50%. | |
<30 | 250 mg PO twice daily or 500 mg PO once daily If used with an HIV PI or COBI, reduce dose by 75% (or consider using azithromycin as alternative). |
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Cycloserine | 10–15 mg/kg/day PO in two divided doses (maximum 1,000 mg/day); start at 250 mg once daily and increase dose per tolerability | 50–80 | Usual dose; consider monitoring serum concentration and toxicities. | |
<50 (not on HD) | Monitor serum concentrations (target peak concentration 20–35 mcg/mL) and adjust dose accordingly. Use with caution in patients with ESRD who are not on dialysis. | |||
HD | 250 mg PO once daily or 500 mg PO three times per week; monitor serum cycloserine concentration (target peak concentration 20–35 mcg/mL). | |||
Emtricitabine (FTC) | One 200–mg tablet PO once daily or 240 mg solution PO once daily |
30–49 | Oral Tablets: 200 mg every 48 hours Oral Solution: 120 mg every 24 hours |
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15–29 | Oral Tablets: 200 mg every 72 hours Oral Solution: 80 mg every 24 hours |
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<15 or HD (administer dose after dialysis) | Oral Tablets: 200 mg every 96 hours Oral Solution: 60 mg every 24 hours |
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Emtricitabine/ Tenofovir Alafenamide (FTC/TAF) (FDC Trade Name: Descovy) Note: Please refer to product information for dosing recommendations for other ARV FDC products containing FTC/TAF. |
One (FTC 200 mg/TAF 25 mg) tablet PO once daily | <30 | Coformulated tablet is not recommended. | |
Emtricitabine/ Tenofovir Disoproxil Fumarate (FTC/TDF) (FDC Trade Name: Truvada) Note: Please refer to product information for dosing recommendations for other ARV FDC products containing FTC/TDF. |
One (FTC 200 mg/TDF 300 mg) tablet PO daily | 30–49 | 1 tablet PO every 48 hours (monitor for worsening renal function or consider switching to TAF) | |
<30 or HD | Do not use coformulated tablet in patients with CrCl <30 mL/min. Use formulation for each component drug and adjust dose according to recommendations for the individual drugs. |
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Entecavir | Usual Dose: 0.5 mg PO once daily For Treatment of 3TC-Refractory HBV or for Patients with Decompensated Liver Disease: 1 mg PO once daily |
30 to <50 | Usual Renal Dose Adjustment:
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10 to <30 | Usual Renal Dose Adjustment:
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<10 or HD or CAPD (administer after HD or CAPD on dialysis day) | Usual Renal Dose Adjustment:
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Ethambutol | For MAI: 15 mg/kg PO daily For MTB: 15–25 mg/kg PO daily (See Table 3 for additional MTB dosing recommendations.) |
<30 or HD | Usual dose PO three times weekly (in patients on HD, give dose after dialysis) Consider TDM to guide optimal dosing. |
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Ethionamide | 15–20 mg/kg PO daily (usually 250–500 mg PO once or twice daily) | <30 or HD | 250–500 mg PO once daily | |
Famciclovir | For Herpes Zoster: 500 mg PO every 8 hours For HSV: 500 mg PO every 12 hours |
40–59 | 500 mg PO every 12 hours | |
20–39 | 500 mg PO every 24 hours | |||
<20 | 250 mg PO every 24 hours | |||
HD | 250 mg PO only on HD days, administer after HD | |||
Fluconazole | 200–1,200 mg PO or IV every 24 hours (dose and route of administration depends on type of OI) | ≤50 | 50% of dose every 24 hours | |
HD | Administer full dose after HD on days of dialysis | |||
Flucytosine | 25 mg/kg PO every 6 hours TDM is recommended for all patients to guide optimal dosing (target peak serum concentration 2 hours after dose: 30–80 mcg/mL). |
21–40 | 25 mg/kg PO every 12 hours | |
10–20 | 25 mg/kg PO every 24 hours | |||
<10 | 25 mg/kg PO every 48 hours | |||
HD | 25–50 mg/kg PO every 48–72 hours; administer dose after HD | |||
Foscarnet | Induction Therapy for CMV Infection: 180 mg/kg/day IV in two divided doses Maintenance Therapy for CMV Infection or for Treatment of HSV Infections: 90–120 mg/kg IV once daily |
Dosage adjustment needed according to calculated CrCl/kg; consult product label for dosing table. | Dosage adjustment needed according to calculated CrCl/kg; consult product label for dosing table. | |
Ganciclovir | Induction Therapy: 5 mg/kg IV every 12 hours | 50–69 | 2.5 mg/kg IV every 12 hours | |
25–49 | 2.5 mg/kg IV every 24 hours | |||
10–24 | 1.25 mg/kg IV every 24 hours | |||
<10 or HD | 1.25 mg/kg IV three times per week; administer dose after HD on days of dialysis | |||
Maintenance Therapy: 5 mg/kg IV every 24 hours | 50–69 | 2.5 mg/kg IV every 24 hours | ||
25–49 | 1.25 mg/kg IV every 24 hours | |||
10–24 | 0.625 mg/kg IV every 24 hours | |||
<10 or HD | 0.625 mg/kg IV three times per week; administer dose after HD on days of dialysis | |||
Lamivudine (3TC) | 300 mg PO every 24 hours | 30–49 | 150 mg PO every 24 hours | |
15–29 | 150 mg PO once, then 100 mg PO every 24 hours | |||
5–14 | 150 mg PO once, then 50 mg PO every 24 hours | |||
<5 or HD | 50 mg PO once, then 25 mg PO every 24 hours; administer dose after HD on dialysis day | |||
Lamivudine/ Tenofovir Disoproxil Fumarate (3TC/TDF) (FDC Trade Names: Cimduo or Temixys) Note: Please refer to product information for dosing recommendations for other ARV FDC products containing 3TC/TDF. |
One (3TC 300 mg/TDF 300 mg) tablet PO every 24 hours | <50 | Coformulated tablet is not recommended. | |
Ledipasvir/ Sofosbuvir | One (ledipasvir 90 mg/sofosbuvir 400 mg) tablet PO once daily | <30 | Coformulated tablet is not recommended. No dose has been established because of up to 20-fold higher sofosbuvir metabolite observed at this level of renal impairment. | |
Levofloxacin | 500 mg (low dose) or 750-1,000 mg (high dose) IV or PO daily | 20–49 | Low Dose: 500 mg once, then 250 mg every 24 hours, IV or PO High Dose: 750 mg every 48 hours IV or PO |
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<20 or CAPD or HD (administer dose after HD or CAPD on days of dialysis) | Low Dose:
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Para-aminosalicylic acid | 8–12 g/day PO in two to three divided doses | <30 or HD | 4 g PO twice daily; administer after HD on days of dialysis | |
Paromomycin | 500 mg PO every 6 hours | <10 | Minimal systemic absorption. No dosage adjustment necessary, but monitor for worsening renal function and ototoxicity in patients with ESRD. | |
Peginterferon Alfa-2a | 180 mcg SQ once weekly | <30 | 135 mcg SQ once weekly | |
HD | 135 mcg SQ once weekly | |||
Peginterferon Alfa-2b | 1.5 mcg/kg SQ once weekly | 30–50 | Reduce dose by 25% | |
10–29 and HD | Reduce dose by 50% | |||
Penicillin G (Potassium or Sodium) |
Neurosyphilis, Ocular Syphilis, or Otosyphilis:
|
10–50 | 2–3 million units every 4 hours or 12–18 million units as continuous infusion |
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<10 | 2 million units every 4–6 hours or 8–12 million units as continuous infusion |
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HD or CAPD | 2 million units every 6 hours or 8 million units as continuous infusion |
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Pentamidine | 4 mg/kg IV every 24 hours | 10–50 | 3 mg/kg IV every 24 hours | |
<10 | 4 mg/kg IV every 48 hours | |||
Posaconazole | IV: 300 mg twice daily on Day 1; then 300 mg once daily Delayed-Release Tablet: 300 mg PO once daily Oral Suspension: 400 mg PO twice daily |
<50 | No dosage adjustment of oral dose in patients with renal insufficiency. Higher variability in serum concentrations observed in patients with CrCl <20 ml/min. Monitor posaconazole concentrations (target trough concentration >1.25 mcg/mL). IV posaconazole is not recommended by the manufacturer because of potential toxicity due to accumulation of sulfobutylether cyclodextrin (vehicle of IV product). However, an observational study did not find worsening in renal function in patients with CrCl <50 ml/min given sulfobutylether cyclodextrin. Switch patients with CrCl <50 ml/min to oral posaconazole when feasible. |
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Pyrazinamide | See Table 3 for weight-based dosing guidelines. | <30 or HD | 25–35 mg/kg/dose three times per week; administer dose after HD on dialysis days | |
Quinidine Gluconate (Salt) Note: 10 mg quinidine gluconate salt = 6.25 mg quinidine base |
10 mg/kg (salt) IV over one to two hours, then 0.02 mg/kg/min (salt) IV for up to 72 hours or until able to take oral meds | <10 | 75% of usual dose | |
HD | 75% of usual dose; some clinicians recommend supplementation with 100–200 mg IV after HD on days of dialysis. Consider TDM for all patients to optimize dosing. |
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Quinine Sulfate | 650 mg salt (524 mg base) PO every 8 hours | <10 or HD | 650 mg once, then 325 mg PO every 12 hours | |
Ribavirin | For Genotypes 1 and 4: 1,000–1,200 mg PO per day in two divided doses (based on weight; see Table 2 for full dosing recommendation) For Genotypes 2 and 3: 400 mg PO twice daily |
30–50 | Alternate dosing 200 mg PO and 400 mg PO every other day | |
<30 or HD | 200 mg PO daily (based on limited data) | |||
Rifabutin | 5 mg/kg PO daily (usually 300 mg PO daily) See Table 3 and Drug-Drug Interactions in the Adult and Adolescent Antiretroviral Guidelines for dosage adjustment based on interactions with ARVs. |
<30 | Consider 50% of dose once daily if toxicity is suspected. Monitor serum concentration and adjust dose as needed. | |
Rifampin | 10 mg/kg PO daily (usually 600 mg PO daily) | <30 or HD | 600 mg once daily, or 600 mg three times per week | |
Sofosbuvir | 400 mg PO daily | <30 | Not recommended. Up to 20-fold higher sofosbuvir metabolite observed in patients with this level of renal impairment. | |
Streptomycin | 15 mg/kg IM or IV every 24 hours or 25 mg/kg IM or IV three times per week |
Use with caution in patients with renal insufficiency. | Adjust dose based on serum concentrations. Administer dose after dialysis on day of dialysis. |
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Sulfadiazine | 1,000–1,500 mg PO every 6 hours (1,500 mg every 6 hours for patients >60 kg) | 10–50 | 1,000–1,500 mg PO every 12 hours (ensure adequate hydration) | |
<10 or HD | 1,000–1,500 mg PO every 24 hours; administer dose after HD on days of dialysis | |||
Telavancin | 10 mg/kg IV every 24 hours | 31-50 | 7.5 mg/kg IV every 24 hours (decreased clinical cure rate with CrCl <50 ml/minute; use with caution) | |
10-30 | 10 mg/kg IV every 48 hours (decreased clinical cure rate with CrCl <50 ml/minute; use with caution) | |||
<10 | Insufficient clinical data to recommend routine use. Use with caution due to decreased clinical cure rate with CrCl < 50 mL/minute. If no other option, consider 10 mg/kg every 48 hours IV or 10 mg/kg IV post-HD three times a week (based on observational study [n = 10]). | |||
Telbivudine | 600 mg PO daily | 30–49 | Oral Tablets: 600 mg PO every 48 hours Oral Solution: 400 mg PO every 24 hours |
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<30 | Oral Tablets: 600 mg PO every 72 hours Oral Solution: 200 mg PO every 24 hours |
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HD | Oral Tablets: 600 mg PO every 96 hours; administer dose after dialysis. Oral Solution: 120 mg PO every 24 hours; administer dose after HD on dialysis day |
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Tenofovir Alafenamide (TAF) | 25 mg PO daily | <15 | Not recommended | |
<15 on HD | No dosage adjustment required. Administer dose after HD on dialysis days. | |||
Tenofovir Disoproxil Fumarate (TDF) | 300 mg PO daily | 30–49 | 300 mg PO every 48 hours (consider switching to TAF for treatment of HBV) | |
10–29 | 300 mg PO every 72–96 hours (consider switching to alternative agent for treatment of HBV) | |||
<10 and not on dialysis | Not recommended | |||
HD | 300 mg PO once weekly; administer dose after dialysis | |||
Tetracycline | 250 mg PO every 6 hours Consider using doxycycline in patients with renal dysfunction. |
10–49 | 250 mg PO every 12–24 hours | |
<10 | 250 mg PO every 24 hours | |||
HD | 250 mg PO every 24 hours; administer dose after dialysis | |||
Trimethoprim/ Sulfamethoxazole (TMP-SMX) | For PCP Treatment:
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15–30 | 5 mg/kg (TMP) IV every 12 hours, or two TMP-SMX DS tablets PO every 12 hours | |
<15 | 5 mg/kg (TMP) IV every 24 hours, or one TMP-SMX DS tablet PO every 12 hours (or two TMP-SMX DS tablets every 24 hours) | |||
HD | 5 mg/kg/day (TMP) IV, or two TMP-SMX DS tablets PO; administer dose after HD on dialysis day. Consider TDM to optimize therapy (target TMP concentrations: 5–8 mcg/mL) |
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For PCP Prophylaxis:
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15–30 | Reduce dose by 50% | ||
<15 | Reduce dose by 50% or use alternative agent | |||
For Toxoplasmosis Encephalitis (TE) Treatment: 5 mg/kg (TMP component) IV or PO every 12 hours | 15–30 | 5 mg/kg (TMP component) IV or PO every 24 hours | ||
<15 | 5 mg/kg (TMP component) IV or PO every 24 hours or use alternative agent | |||
For TE Chronic Maintenance Therapy:
|
15–30 | Reduce dose by 50% | ||
<15 | Reduce dose by 50% or use alternative agent | |||
For Toxoplasmosis Primary Prophylaxis: One TMP-SMX DS tablet PO daily | 15-30 | Reduce dose by 50% | ||
<15 | Reduce dose by 50% or use alternative agent | |||
Valacyclovir | For Herpes Zoster: 1 g PO three times daily | 30–49 | 1 g PO every 12 hours | |
10–29 | 1 g PO every 24 hours | |||
<10 | 500 mg PO every 24 hours | |||
HD | 500 mg PO every 24 hours; dose after HD on dialysis days | |||
Valganciclovir | Induction Therapy: 900 mg PO twice daily Maintenance Therapy: 900 mg PO once daily |
40–59 | Induction: 450 mg PO twice daily Maintenance: 450 mg PO daily |
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26–39 | Induction: 450 mg PO daily Maintenance: 450 mg PO every 48 hours |
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10–25 | Induction: 450 mg PO every 48 hours Maintenance: 450 mg PO twice weekly |
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<10 and not on dialysis | Induction: Not recommended Maintenance: Not recommended |
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HD Note: Clinical efficacy of these doses has not been established. |
Induction: 200 mg (oral powder formulation) PO three times per week after HD Maintenance: 100 mg (oral powder formulation) PO three times per week after HD |
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Voriconazole | 6 mg/kg IV every 12 hours for two doses, then 4 mg/kg IV every 12 hours or 200–300 mg PO every 12 hours |
<50 | IV voriconazole is not recommended by the manufacturer because of potential toxicity due to accumulation of sulfobutylether cyclodextrin (vehicle of IV product). An observational study did not find worsening in renal function in patients with CrCl <50 mL/min. Switch patients with CrCl <50 mL/min to oral voriconazole when feasible. No need for dosage adjustment when the oral dose is used. Adjust dose based on serum concentrations. |
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Key: 3TC = lamivudine; ARV = antiretroviral; CAPD = continuous ambulatory peritoneal dialysis; CMV = cytomegalovirus; COBI = cobicistat; CrCl = creatinine clearance; DS = double strength, ESRD = end-stage renal disease; FDC = fixed-dose combination; FTC = emtricitabine; HBV = hepatitis B virus; HD = hemodialysis; HSV = herpes simplex virus; IM = intramuscular; IV = intravenous; MAI = Mycobacterium avium intracellulare; MTB = Mycobacterium tuberculosis; N/A = not applicable; OI = opportunistic infection; PD = peritoneal dialysis; PCP = Pneumocystis pneumonia; PI = protease inhibitor; PO = orally; SCr = serum creatinine; SQ = subcutaneous; TAF = tenofovir alafenamide; TDF = tenofovir disoproxil fumarate; TDM = therapeutic drug monitoring; TMP-SMX = trimethoprim-sulfamethoxazole; VZV = varicella zoster virus |
*Creatinine Clearance Calculation | |
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Male: (140 - age in years) x (weight in kg) 72 x (serum creatinine) |
Female: (140 - age in years) x (weight in kg) x (0.85) 72 x (serum creatinine) |