Pharmacokinetics of intravenously and intramuscularly administered cefepime in infants and children
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Updated: Aug 4, 2026

Intravenous Injections in Neonatal Mice
Published on: November 11, 2014
M D Reed1, T S Yamashita, C K Knupp
1Center for Drug Research, Rainbow Babies and Childrens Hospital, Department of Pediatrics, School of Medicine, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
Insights
This study on cefepime pharmacokinetics in infants and children found that a 50 mg/kg dose every 12 hours is effective for treating infections. Cefepime dosing can be simplified for patients two months and older.
Area of Science:
- Pharmacology
- Pediatric Infectious Diseases
- Clinical Pharmacy
Background:
- Cefepime is a broad-spectrum cephalosporin antibiotic used to treat various bacterial infections.
- Understanding cefepime pharmacokinetics in pediatric populations is crucial for optimizing dosing regimens.
- Previous studies have indicated variability in cefepime disposition based on age and renal function.
Purpose of the Study:
- To characterize the pharmacokinetic properties of cefepime in infants and children.
- To evaluate cefepime pharmacokinetics after single and multiple intravenous doses, and after intramuscular administration.
- To determine an optimal cefepime dosing strategy for pediatric patients.
Main Methods:
- 37 infants and children (2.1 months to 16.4 years) with normal renal function received cefepime 50 mg/kg intravenously every 8 hours.
- Pharmacokinetics were assessed after the first dose (n=35) and at steady-state (n=31).
- Eight subjects received an intramuscular dose to assess disposition and bioavailability.
Main Results:
- Elimination half-life averaged 1.7 hours, steady-state volume of distribution was 0.35 L/kg, and total body clearance was 3.1 mL/min/kg.
- Pharmacokinetics were similar between first-dose and steady-state evaluations, with slightly longer half-life and MRT in younger children (<6 months).
- Intramuscular administration resulted in slightly prolonged half-life and MRT, with an average bioavailability of 82%.
Conclusions:
- The pharmacokinetic data support a simplified cefepime dosing strategy for pediatric patients aged two months and older.
- A cefepime dose of 50 mg/kg every 12 hours is recommended for treating infections caused by susceptible pathogens (MIC ≤ 8 mg/L).
- This dosing regimen aims to ensure therapeutic efficacy while considering the pharmacokinetic profile in the pediatric population.
Abstract:
The pharmacokinetic characteristics of cefepime were determined after first dose (n = 35) and again under steady-state conditions (n = 31) with a group of 37 infants and children. In eight subjects, a cefepime dose given by intramuscular injection was substituted for an intravenous dose, and disposition characteristics were studied again. Study subjects ranged in age from 2.1 months to 16.4 years, and all had normal renal function. Each patient received 50 mg of cefepime/kg of body weight intravenously every 8 h, up to a total maximum individual dose of 2 g. With the exception of one study patient who received a single cefepime dose for surgical prophylaxis, the patients received cefepime for 2 to 13 days. Elimination half-life (t1/2), steady-state volume of distribution, total body clearance, and renal clearance after first dose administration averaged 1.7 h, 0.35 liter/kg, and 3.1 and 1.9 ml/min/kg, respectively. Although cefepime t1/2 and mean residence time (MRT) were slightly longer for subjects <6 months of age than for older subjects, no differences in cefepime disposition characteristics between first dose and steady-state evaluations were observed. t1/2 (1.8 versus 1.9 h) and MRT (2.3 versus 3.2 h) were slightly prolonged after intramuscular administration, reflecting the influence of absorption from the intramuscular injection site on cefepime elimination. Bioavailability after intramuscular administration averaged 82% (range, 61 to 124%). Fifty-seven percent of the first dose and 88.9% of the last dose were recovered as unchanged drug in urine over the 8- and 24-h sampling periods, respectively. These pharmacokinetic data support a single cefepime dosing strategy for patients > or =2 months of age. The integration of the cefepime pharmacokinetic data generated in our study with the MICs for important pathogens responsible for infections in infants and children supports the administration of a dose of 50 mg of cefepime/kg every 12 h for patients > or =2 months of age to treat infections caused by pathogens for which cefepime MICs are < or =8 mg/liter.
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