What is the recommended dosing regimen of ceftazidime‑avibactam, including renal dose adjustments, for treating complicated intra‑abdominal infections, complicated urinary tract infections, and hospital‑acquired or ventilator‑associated pneumonia?

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Last updated: September 14, 2026 • View editorial policy

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Ceftazidime-Avibactam Dosing Regimen

For adults with normal renal function (CrCl >50 mL/min), administer ceftazidime-avibactam 2.5 grams (ceftazidime 2 grams + avibactam 0.5 grams) IV every 8 hours as a 2-hour infusion. 1

Standard Dosing by Indication

Complicated Intra-Abdominal Infections (cIAI)

  • Dose: 2.5 g IV every 8 hours over 2 hours
  • Duration: 5-14 days 2, 1
  • Critical requirement: Must be combined with metronidazole 500 mg IV every 6-8 hours for anaerobic coverage 2, 1

Complicated Urinary Tract Infections (cUTI) including Pyelonephritis

  • Dose: 2.5 g IV every 8 hours over 2 hours
  • Duration: 5-10 days (typically 7-14 days) 2, 1
  • No additional anaerobic coverage needed

Hospital-Acquired/Ventilator-Associated Pneumonia (HAP/VAP)

  • Dose: 2.5 g IV every 8 hours over 2 hours
  • Duration: 10-14 days (typically 7-14 days) 2, 1
  • No additional anaerobic coverage needed

Renal Dose Adjustments (Adults)

Monitor creatinine clearance daily in patients with changing renal function and adjust dosing accordingly. 1 This is particularly critical as renal function can improve rapidly during treatment, potentially leading to subtherapeutic drug levels.

CrCl (mL/min) Dose Frequency
31-50 1.25 g (ceftazidime 1 g + avibactam 0.25 g) Every 8 hours
16-30 0.94 g (ceftazidime 0.75 g + avibactam 0.19 g) Every 12 hours
6-15 0.94 g (ceftazidime 0.75 g + avibactam 0.19 g) Every 24 hours
≤5 (including hemodialysis) 0.94 g (ceftazidime 0.75 g + avibactam 0.19 g) Every 48 hours

1

For hemodialysis patients: Administer after dialysis on dialysis days, as both drugs are removed by hemodialysis. 1

Pediatric Dosing

Ages 2 to <18 years (eGFR >50 mL/min/1.73 m²)

  • Dose: 62.5 mg/kg (ceftazidime 50 mg/kg + avibactam 12.5 mg/kg)
  • Maximum: 2.5 g per dose
  • Frequency: Every 8 hours over 2 hours
  • Duration: Same as adults by indication 1

Ages 6 months to <2 years (no renal impairment)

  • Dose: 62.5 mg/kg (ceftazidime 50 mg/kg + avibactam 12.5 mg/kg)
  • Frequency: Every 8 hours over 2 hours 1

Ages 3 months to <6 months

  • Dose: 50 mg/kg (ceftazidime 40 mg/kg + avibactam 10 mg/kg)
  • Frequency: Every 8 hours over 2 hours 1

Ages >28 days to <3 months

  • Dose: 37.5 mg/kg (ceftazidime 30 mg/kg + avibactam 7.5 mg/kg)
  • Frequency: Every 8 hours over 2 hours 1

Ages ≤28 days (gestational age ≥31 weeks)

  • Dose: 25 mg/kg (ceftazidime 20 mg/kg + avibactam 5 mg/kg)
  • Frequency: Every 8 hours over 2 hours 1

For pediatric cIAI: Add metronidazole 10 mg/kg IV every 8 hours 1

Critical Clinical Considerations

Infusion Duration

Always infuse over 2 hours. 1 Extended infusion (3 hours) may be considered for critically ill patients or those with high MIC pathogens to optimize pharmacodynamic target attainment, though this is not standard FDA labeling. 2

Specific Pathogen Considerations

  • Carbapenem-resistant Enterobacterales (CRE): Standard dosing is appropriate for KPC and OXA-48 producers 2, 3
  • Metallo-β-lactamase producers (NDM, VIM): Ceftazidime-avibactam is NOT effective as monotherapy; requires combination with aztreonam 4, 3
  • Difficult-to-treat Pseudomonas aeruginosa: Standard dosing is appropriate 2

Common Pitfalls to Avoid

  1. Forgetting metronidazole for cIAI: Ceftazidime-avibactam lacks anaerobic coverage—always add metronidazole for intra-abdominal infections 2, 1
  2. Not adjusting for renal function: Both drugs are renally cleared; failure to adjust leads to toxicity 1
  3. Not monitoring changing renal function: Critically ill patients often have fluctuating renal function requiring daily reassessment 1, 5
  4. Using for MBL producers without aztreonam: This will result in treatment failure 4, 3

Special Populations

CVVH/CRRT patients: Clearance increases significantly during continuous renal replacement therapy. Standard dosing may be inadequate; consider therapeutic drug monitoring if available. 6, 7

VA-ECMO patients: Drug clearance may change after ECMO weaning; reassess dosing if therapy extends beyond ECMO support. 7

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