The study by Nahata et al. (N=9, age 10 months – 10 years) shows that the elimination half-life of cefazolin in children averages 1.68 ± 0.55 hours. The total clearance and the apparent volume of distribution are 1.43 ± 0.54 ml/min/kg and 0.08 ± 0.03 l/kg respectively.
The study by Deguchi et al. shows that the percentage of the free fraction of cefazolin varies widely in neonates. The volume of distribution in neonates is 0.21–0.37 l/kg.
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No information is present at this moment.
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| Infections by very sensitive Gram-positive microorganisms |
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| Infections by less sensitive Gram-positive microorganisms and Gram-negative pathogens |
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| Perioperative prophylaxis |
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Dose adjustments <14 years
Cl 40 - 70 mL/min: Start with normal single dose, continue at 60 % of daily dose with divided in 2 doses with dosing interval of 12 hours
Cl 20 - 40 mL/min: Start with normal single dose, continue at 25 % of daily dose with divided in 2 doses with dosing interval of 12 hours
Cl < 20 mL/min: Start with normal single dose, continue at 10 % of daily dose, with dosing interval of 24hours
Dose adjustments ≥ 14 years
Cl 35 - 54 mL/min: Normal daily dose (no dose adjustment), dosing interval at 8 hours
Cl 10 - 34 mL/min: Start with normal single dose, continue at 50% of normal daily dose, dosing interval at 12 hours
Cl < 10 mL/min: Start with normal single dose, continue at 50% of normal daily dose, dosing interval at 18-24 hours
[SmPC Cefazolin Fresenius]
Nephrotoxic symptoms (renal function disorder, tubular necrosis, interstitial nephritis) occur primarily at high dosages, in pre-existing renal function disorders and in concomitant treatment with other nephrotoxic substances. Convulsions can occur at very high doses. The time above the MIC determines the effect.
No data known
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The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here
Thrombophlebitis, fever, nausea, vomiting, diarrhoea, obstipation, abnormal blood counts, temporarily elevated liver enzymes.
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The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here
No information available on specific contra indications in children.
The complete list of all warnings and precautions can be found in the national Summary of Product Characteristics (SmPC) – click here
Cephalosporins can in general be given to patients who are hypersensitive to penicillin, although cross-reactions have been reported. Special care is indicated in patients who previously had anaphylactic responses to penicillins. Pseudomembranous colitis may occur during antibiotic use. If pseudomembranous colitis develops, the cefazolin treatment should be discontinued and an appropriate therapy started. In long-term use, checks of the blood counts and hepatic and renal function are desirable.
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The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
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| First-generation cephalosporins | ||
|---|---|---|
| J01DB01 | ||
| Second-generation cephalosporins | ||
|---|---|---|
| J01DC02 | ||
| Third-generation cephalosporins | ||
|---|---|---|
| J01DD08 | ||
| J01DD01 | ||
| J01DD52 | ||
| J01DD02 | ||
| J01DD04 | ||
| Carbapenems | ||
|---|---|---|
| J01DH02 | ||
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