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[Pharmacokinetic and clinical studies of cefprozil fine granules in children]
Insights
Cefprozil (CFPZ) is a new oral antibiotic showing high effectiveness and safety in pediatric patients. This study found CFPZ to be a suitable treatment for moderate respiratory and urinary tract infections in children.
Area of Science:
- Pharmacology
- Pediatrics
- Infectious Diseases
Background:
- Cefprozil (CFPZ) is a novel oral cephem antibiotic.
- It lacks an ester linkage, differentiating it from other cephem antibiotics.
- This study evaluates CFPZ in pediatric patients.
Purpose of the Study:
- To assess the pharmacokinetics of Cefprozil in children.
- To evaluate the clinical efficacy and safety of Cefprozil in treating pediatric infections.
- To determine the bacteriological eradication rate of Cefprozil.
Main Methods:
- Pharmacokinetic analysis involved administering CFPZ fine granules at 7.5 mg/kg and 10 mg/kg doses.
- Clinical efficacy was assessed in 22 pediatric patients with various infections.
- Bacteriological efficacy was determined by monitoring bacterial eradication, replacement, and persistence.
Main Results:
- Peak serum concentrations of CFPZ were observed at 1-2 hours post-administration.
- The average half-life ranged from 0.90 to 1.29 hours, with approximately 45% urinary excretion within 6 hours.
- Clinical response was excellent in 14 patients, good in 5, and fair in 1, with a bacteriological eradication rate of 76.5%.
Conclusions:
- Cefprozil demonstrates favorable pharmacokinetic properties in pediatric patients.
- CFPZ is highly effective and safe for treating moderate respiratory and urinary tract infections in children.
- No adverse reactions were reported, supporting its safety profile.
Abstract:
Cefprozil (CFPZ, BMY-28100) is a new oral cephem antibiotic without an ester linkage. Pharmacokinetic and clinical studies using CFPZ 10% fine granules were performed in pediatric patients. 1. Pharmacokinetic investigation Peak serum concentrations of CFPZ after dose of 7.5 mg/kg and 10 mg/kg were, respectively, 3.65 +/- 0.24 micrograms/ml and 6.38 +/- 3.23 micrograms/ml at 1-2 hours. The average half-life with 7.5 mg/kg administration was 0.90 +/- 0.16 hours and that with 10 mg/kg was 1.29 +/- 0.50 hours. The urinary excretion of CFPZ was about 45% (35.3-50.0%) in 6 hours. 2. Clinical investigation Enrolled in the study were 22 patients including 4 with pharyngitis, 3 with tonsillitis, 3 with bronchitis, 5 with pneumonia, 4 with urinary tract infection, and 1 each with pertussis, purulent lymphadenitis and otitis media. Responses were excellent in 14 patients, good in 5 patients and fair in 1 patient. In the assessment of the bacteriological efficacy, 8 out of 17 strains of organism identified previous to the treatment were eradicated, 5 strains were found replaced by other bacteria and 4 strains persisted, hence the eradication rate was 76.5%. 3. No adverse reactions attributable to the drug were observed. From the above results, it has been concluded that CFPZ is a highly effective and safe agent for moderate respiratory and urinary tract infections in children.
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