Section VI — Safe Prescribing
Renal Drug Dosing
GFR-adjusted dosing for high-risk medications — anticoagulants and antibiotics — to reduce accumulation, bleeding, and nephrotoxicity. Match the patient's eGFR band to the correct column.
eGFR ≥ 50
Normal / mild
eGFR 30–49
Moderate
eGFR < 30 / HD
Severe / dialysis
Tip: Use the eGFR calculator (right edge of screen) to determine the patient's band before selecting a dose.
Medication
Standard Dose
eGFR ≥ 50
eGFR 30–49
eGFR < 30 / HD
Clinical Note
Warfarin
AnticoagulantVitamin K antagonist
2–10 mg PO daily
No adjustment (INR-guided)
No adjustment
No adjustment
Monitor INR; ↑bleeding risk in CKD; avoid rapid shifts
Enoxaparin
AnticoagulantLMWH
1 mg/kg SC q12h (tx); 40 mg q24h (prophylaxis)
Standard
Standard
1 mg/kg q24h (tx); 30 mg q24h (prophylaxis); dose after HD
Contraindicated if CrCl <30 without dose reduction; ↑bleeding risk
Heparin (UFH)
AnticoagulantUnfractionated heparin
80 U/kg bolus → 18 U/kg/hr IV infusion
No adjustment
No adjustment
No adjustment; safe in HD
Titrate to aPTT/anti-Xa; no renal clearance but ↑bleeding risk in CKD
Apixaban
AnticoagulantDOAC (Factor Xa)
5 mg PO BID (AF)
Standard
5 mg BID; → 2.5 mg BID if 2 of: age ≥80, ≤60 kg, SCr ≥1.5
5 mg BID (↓ to 2.5 mg BID per criteria); use caution on HD
Avoid CrCl <15 per some guidance; reassess bleeding risk annually
Rivaroxaban
AnticoagulantDOAC (Factor Xa)
20 mg PO daily (AF)
20 mg daily
15 mg daily
15 mg daily (CrCl 15–50); avoid if CrCl <15
Avoid CrCl <15; ↑bleeding risk; not dialyzable
Dabigatran
AnticoagulantDOAC (direct thrombin)
150 mg PO BID (AF)
150 mg BID
150 mg BID (110 mg BID if high bleeding risk)
75 mg BID (CrCl 15–30); avoid if CrCl <15
Contraindicated CrCl <15; ~50% dialyzable — give after HD
Edoxaban
AnticoagulantDOAC (Factor Xa)
60 mg PO daily (AF)
60 mg daily
30 mg daily
30 mg daily (CrCl 15–50); avoid if CrCl <15
Avoid CrCl <15; ineffective if CrCl >95
Vancomycin
AntibioticGlycopeptide
15–20 mg/kg IV q8–12h
Standard, trough-based
Extend interval q12–24h
Per level; HD: redose at trough 15–20 mg/L (q3–7 days)
Therapeutic drug monitoring; nephrotoxic; avoid concurrent nephrotoxins
Gentamicin / Tobramycin
AntibioticAminoglycoside
5–7 mg/kg IV q24h (extended interval)
q24h
q24–36h
Per level; HD: 2–3 mg/kg after dialysis
Nephro- & ototoxic; limit ≤5–7 days; monitor levels + trough
Cefepime
Antibioticβ-lactam (4th gen ceph)
2 g IV q8h (severe)
Standard
q24h
q48h; HD: 1 g q24h (supplement post-HD)
Dose to eGFR to avoid neurotoxicity (encephalopathy, myoclonus)
Levofloxacin
AntibioticFluoroquinolone
750 mg IV/PO q24h
Standard
750 mg q48h
750 mg load → 500 mg q48h; HD: 500 mg q48h
Tendonopathy; QT prolongation; CNS effects; dysglycemia
Ciprofloxacin
AntibioticFluoroquinolone
400 mg IV q8h or 500–750 mg PO q12h
Standard
q8–12h
q12–18h; HD: q24h (post-HD)
Tendonopathy; QT prolongation; avoid with theophylline
Meropenem
AntibioticCarbapenem
1 g IV q8h
Standard
1 g q12h
500 mg q12h (CrCl 10–29); <10: 500 mg q24h; HD: 500 mg q24h post-HD
Seizure risk in high dose / renal impairment; reduce dose
Piperacillin-tazobactam
Antibioticβ-lactam + inhibitor
3.375–4.5 g IV q6–8h
Standard
q8h
q12h; HD: 2.25 g q8h (post-HD, extended infusion)
Monitor Na load; adjust for renal function to prevent neurotoxicity
Trimethoprim-Sulfamethoxazole
AntibioticSulfonamide
8–20 mg/kg/day TMP divided
Standard
Half dose or q12–24h
Avoid if possible; half dose; HD: dose after dialysis
Blocks Cr secretion (false ↑Cr) & causes hyperkalemia; avoid in late CKD
Nitrofurantoin
AntibioticUrinary antiseptic
100 mg PO BID × 5 days (uncomplicated UTI)
Standard
Avoid (CrCl <30)
Contraindicated
Ineffective + peripheral neuropathy risk if CrCl <30; cystitis only
Amoxicillin-clavulanate
Antibioticβ-lactam + inhibitor
875/125 mg PO BID
Standard
q12h
q24h; HD: q24h (post-HD)
Clavulanate accumulates; hepatotoxicity risk with prolonged use
Metronidazole
AntibioticNitroimidazole
500 mg IV/PO q8h
Standard
Standard
Standard; HD: supplement post-HD
Minimal adjustment needed; supplement after HD
Aztreonam
AntibioticMonobactam
2 g IV q8h
Standard
q12h
q24h; HD: load 1–2 g → 1 g q12h
Safe in penicillin-allergic patients; adjust per CrCl
Darbepoetin (Aranesp)
ESRDErythropoiesis-stimulating agent
0.45 mcg/kg SC/IV weekly (naïve)
Per Hgb protocol
No renal clearance
Same; HD: give post-dialysis
Target Hgb 10–11 g/dL; hold if >11.5; see ESA calculator for conversion
Epoetin alfa (Epogen)
ESRDESA (recombinant EPO)
50–100 U/kg SC/IV 3×/week
Per Hgb protocol
No renal clearance
Same; HD: IV post-dialysis
Convert to darbepoetin: weekly units ÷ 200 = mcg/week
Methoxy PEG-epoetin β (Mircera)
ESRDESA (long-acting)
0.6 mcg/kg SC/IV q2weeks (naïve)
Per Hgb protocol
No renal clearance
Same; HD: IV post-dialysis; monthly once stable
C3 pegylated; less frequent dosing; same CV warnings
Calcitriol (Rocaltrol)
ESRDActive vitamin D (1,25-OH₂D)
0.25 mcg PO daily or 0.5 mcg 3×/wk
Per PTH/Ca/Phos
Per PTH
Titrate to PTH; hold if Ca↑/Phos↑
Use CKD-MBD calculator; monitor Ca, Phos, PTH q3mo
Paricalcitol (Zemplar)
ESRDVitamin D analog (19-nor D₂)
1 mcg IV/PO daily or 2–4 mcg 3×/wk (HD)
Per PTH
Per PTH
Titrate to PTH; less Ca/Phos effect
Less hypercalcemia/hyperphosphatemia than calcitriol
Cinacalcet (Sensipar)
ESRDCalcimimetic
30 mg PO daily → titrate q2–4wk
Standard
Standard
Standard; titrate to PTH ≥150 & Ca ≥8.4
Lowers PTH & Ca; risk hypocalcemia; avoid in primary HPT post-transplant
Sevelamer carbonate (Renvela)
ESRDNon-calcium phosphate binder
800–1600 mg PO with meals
Standard
Standard
Standard; titrate to Phos
No calcium load; lowers LDL; high pill burden
Lanthanum carbonate (Fosrenol)
ESRDNon-calcium phosphate binder
500–1000 mg PO with meals
Standard
Standard
Standard; chew tablets
Potent binder; minimal systemic absorption; GI effects
Sucroferric oxyhydroxide (Velphoro)
ESRDIron-based phosphate binder
500 mg PO 3×/day with meals
Standard
Standard
Standard; low pill burden
Iron-based; minimal absorption; discolors stools
Ferric carboxymaltose (Injectafer)
ESRDIV iron
750 mg IV ×2 (≥7 d apart)
Per iron indices
Per iron indices
HD: 100 mg IV q1–2wk to TSAT 30–50%
Target TSAT 30–50% & ferritin 200–500 ng/mL; test dose obsolete
Clinical disclaimer: These ranges are a quick-reference for adult dosing only. Always confirm against current package inserts, institutional protocols, and the patient's actual eGFR, weight, and indication. Therapeutic drug monitoring (vancomycin, aminoglycosides) is required — adjust to levels, not the table alone.
References & Further Reading
- 01Drug Dosing in Patients with CKD and Requiring Dialysis — KDIGO Clinical Practice Guideline — Kidney International Reports (2019)
- 02Sanford Guide to Antimicrobial Therapy (Renal Dosing) — Sanford Guide (2023)
- 03FDA Drug Labeling — Renal Impairment Dosing — U.S. Food & Drug Administration (current)
- 04Aronoff GR et al. Drug Prescribing in Renal Failure: Dosing Guidelines for Adults — American College of Physicians (2007)
- 05KDIGO Clinical Practice Guideline for Anemia in CKD — KDIGO (2012)
- 06KDIGO Clinical Practice Guideline for CKD-MBD — KDIGO (2017)