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Published on: December 27, 2016
[Clinical studies on cefprozil granules]
Insights
Cefprozil granules demonstrated 100% clinical efficacy in pediatric bacterial infections, with no observed side effects. This study highlights its potential as a well-tolerated treatment option for children.
Area of Science:
- Pediatric Infectious Diseases
- Pharmacology
- Bacteriology
Background:
- Bacterial infections are common in pediatric patients.
- Effective and safe antimicrobial agents are crucial for treating pediatric infections.
- Cefprozil is a cephalosporin antibiotic with a broad spectrum of activity.
Purpose of the Study:
- To evaluate the clinical efficacy and safety of cefprozil granule preparation in pediatric patients with bacterial infections.
- To assess the bacteriological eradication rates of cefprozil against common pediatric pathogens.
Main Methods:
- Oral administration of cefprozil granule preparation to 16 pediatric patients (8 months to 9 years 6 months).
- Daily doses ranged from 29.4 to 35.7 mg/kg, divided into 3 or 4 doses.
- Clinical efficacy, bacteriological response, and adverse events were monitored.
Main Results:
- Overall clinical efficacy rate was 100% (9 excellent, 7 moderate).
- Bacteriological eradication rate was 68.8% against 17 pathogen strains, including Haemophilus influenzae, Streptococcus pyogenes, and Staphylococcus aureus.
- No significant side effects were observed; abnormal laboratory findings were transient and not clinically significant.
- Palatability was not an issue, with no drug refusal due to taste or odor.
Conclusions:
- Cefprozil granule preparation is highly effective and well-tolerated for treating pediatric bacterial infections.
- The drug demonstrated a favorable safety profile and good palatability in the pediatric population.
- Cefprozil shows promise as a valuable therapeutic option for pediatric bacterial infections.
Abstract:
Cefprozil granule preparation was administered orally to 16 patients (ages ranging 8 months to 9 years and 6 months) with pediatric bacterial infections at daily dose levels between 29.4 and 35.7 mg/kg divided into 3 or 4 doses. The following results were obtained. 1. Sixteen patients including 5 with pharyngitis, 3 with tonsillitis, 3 with lacunar tonsillitis, 2 with pneumonia, 2 with contagious impetigo and 1 with scarlet fever were treated. Clinical effects were excellent in 9 cases and moderate in 7, with an overall efficacy rate of 100%. 2. Organisms suspected as pathogens included 17 strains (10 strains of haemophilus influenzae, 2 of Haemophilus parainfluenzae, 3 of Streptococcus pyogenes and 2 of Staphylococcus aureus). Bacteriologically, eradication of pathogens were observed for 11 strains, but no changes were obtained for 5 (all Haemophilus), and unknown results were obtained for 1, thus the eradication rate was 68.8%. 3. No side effects were observed. Abnormal laboratory test results included 2 cases of increase in platelets, and 2 of increase in eosinophils, but those were not significant. 4. No refusal of the drug occurred due to its taste or odor.
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