What is the recommended use and dosage of Cefepime (Cefepime) Tazobactam (Tazobactam) injection?

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Cefepime-Tazobactam Injection: Recommended Use and Dosage

Cefepime-tazobactam is recommended for complicated infections caused by gram-negative pathogens, particularly for multidrug-resistant organisms, with a standard adult dosage of 2g cefepime/2g tazobactam administered intravenously every 8 hours over a 90-minute infusion. 1

Indications for Use

Cefepime-tazobactam is indicated for the treatment of:

  • Complicated urinary tract infections (cUTIs) including pyelonephritis 2, 3
  • Complicated intra-abdominal infections (in combination with metronidazole) 4
  • Healthcare-associated infections with risk of resistant organisms 5
  • Infections caused by ESBL-producing Enterobacterales resistant to other antibiotics 1, 6
  • Pseudomonas aeruginosa infections, including carbapenem-resistant strains 2

Dosage Recommendations

Standard Adult Dosing

  • Standard dose: 2g cefepime/2g tazobactam IV every 8 hours 1, 6
  • Infusion time: 90 minutes (prolonged infusion) 1
  • Duration: 7-10 days for most infections 2, 4

Renal Dosage Adjustments

Based on creatinine clearance (CrCl) 4, 6:

  • CrCl 30-59 mL/min: 1g every 8 hours
  • CrCl 15-29 mL/min: 500mg every 8 hours
  • CrCl 8-14 mL/min: 500mg every 12 hours
  • Hemodialysis patients: 500mg every 12 hours, with additional dose after dialysis

Special Populations

  • Augmented renal clearance (CrCl 120-180 mL/min): Standard dose with prolonged 4-hour infusion 6
  • Critically ill patients: May require higher end of dosing range with prolonged infusion to ensure adequate drug concentrations 2

Clinical Efficacy

Cefepime-tazobactam has demonstrated:

  • Superior efficacy compared to piperacillin-tazobactam in complicated UTIs, with 79.1% vs 58.9% overall treatment success in a phase 3 clinical trial 3
  • Activity against 97.6% of Enterobacterales isolates at ≤8 mg/L, comparable to meropenem (97.0%) and superior to piperacillin-tazobactam (88.0%) 1
  • Effectiveness against multidrug-resistant Pseudomonas aeruginosa, inhibiting 92.2% of isolates at ≤16 mg/L 1

Specific Use Cases

For Carbapenem-Resistant Pseudomonas aeruginosa (CRPA)

  • Cefepime 2g IV every 8-12 hours is recommended as an alternative treatment option 2
  • For difficult-to-treat Pseudomonas aeruginosa (DTR-PA), may be used in combination with other agents 2

For Complicated UTIs/Pyelonephritis

  • Cefepime 2g IV every 8-12 hours is recommended for empiric parenteral therapy 2
  • Higher dose (2g) is recommended over lower doses studied in clinical trials 2

For Intra-abdominal Infections

  • Cefepime 2g IV every 8 hours plus metronidazole 500mg every 6 hours is recommended for healthcare-associated infections or critically ill patients 2, 5

Potential Pitfalls and Considerations

  • Resistance development: Monitor local resistance patterns, particularly in healthcare settings with high prevalence of ESBL-producing organisms 5
  • Duration of therapy: Limit to 7 days when adequate source control is achieved; extended courses may be needed for immunocompromised patients or inadequate source control 5
  • Drug interactions: Avoid concurrent administration with other IV solutions through the same line 4
  • Monitoring: Regular assessment of renal function is necessary, with dose adjustments as needed 5, 4

Advantages Over Alternative Therapies

  • Carbapenem-sparing option: Helps preserve carbapenems for more resistant infections 1
  • Broad spectrum coverage: Active against many ESBL-producing organisms that are resistant to piperacillin-tazobactam 1, 6
  • Superior efficacy: Demonstrated better outcomes than piperacillin-tazobactam in complicated UTIs 3

Cefepime-tazobactam represents an important therapeutic option for serious gram-negative infections, particularly in settings with high rates of resistance to other β-lactam/β-lactamase inhibitor combinations.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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