Ceftolozane/Tazobactam Dosing for Adults with Normal Renal Function
The recommended dose of ceftolozane/tazobactam for adults with normal renal function is 1.5 g (1 g ceftolozane/0.5 g tazobactam) administered intravenously every 8 hours. 1
Dosing Recommendations by Indication
Standard Indications
- For complicated urinary tract infections and complicated intra-abdominal infections:
Hospital-Acquired/Ventilator-Associated Pneumonia
- For nosocomial pneumonia (hospital-acquired or ventilator-associated):
Renal Dosage Adjustments
Ceftolozane/tazobactam requires dose adjustment based on renal function:
| Creatinine Clearance (CrCl) | Recommended Dose |
|---|---|
| >50 mL/min | 1.5 g every 8 hours |
| 30-50 mL/min | 750 mg every 8 hours |
| 15-29 mL/min | 375 mg every 8 hours |
| ESRD on hemodialysis | Loading dose of 750 mg, then 150 mg every 8 hours [3,5] |
Administration Guidelines
- Reconstitute with 10 mL of sterile water or compatible diluent
- Further dilute to 50-150 mL in compatible IV solution
- Administer by IV infusion over 1 hour 6
- For patients on hemodialysis, administer dose after completion of dialysis 3
Clinical Considerations
- Ceftolozane/tazobactam is particularly effective against multidrug-resistant Pseudomonas aeruginosa, including carbapenem-resistant strains 1, 2
- It can be used as a carbapenem-sparing regimen in critically ill patients with healthcare-associated infections 1
- For intra-abdominal infections, combination with metronidazole (500 mg IV every 6 hours) is recommended for anaerobic coverage 1
Pharmacokinetic Considerations
- Linear pharmacokinetics with a plasma half-life of approximately 2.3 hours 2
- Primary elimination is via renal excretion (≥92%) 2
- Low plasma protein binding (approximately 20%) 2
Monitoring
- Regular assessment of renal function is recommended during therapy
- Monitor for adverse effects, particularly in patients with renal impairment
- No routine therapeutic drug monitoring is required for patients with normal renal function
The recommended dosing of ceftolozane/tazobactam is supported by population pharmacokinetic studies demonstrating high probability of target attainment at these doses across various patient populations 4, 7.