dose recommendation of formulary compared to licensed use (on-label versus off-label)
No information is present at this moment.
Available formulations
No information is present at this moment.
Dosages
Go to:
Bacterial infections
Intravenous
<
1 week
and
weight at birth
<
2.5 kg
Initial dose
20
mg/kg/day
in 2
doses. Run in over 1-2 hours. Subsequent dosing guided by TDM.
There is currently no consensus about the dosage for full-term neonates and premature infants. Studies into this are ongoing and when more is known, the dosage will be adjusted in line with the results of the research.
Initial dose:
30
mg/kg/day
in 3
doses. Allow to run in over 1-2 hours. Subsequent dosing guided by TDM.
There is currently no consensus about the dosage for full-term neonates and premature infants. Studies into this are ongoing and when more is known, the dosage will be adjusted in line with the results of the research.
Initial dose
32
mg/kg/day
in 4
doses. Allow to run in over 1-2 hours. Subsequent dosing guided by TDM.
There is currently no consensus about the dosage for full-term neonates and premature infants. Studies into this are ongoing and when more is known, the dosage will be adjusted in line with the results of the research.
Initial dose:
48
mg/kg/day
in 4
doses. Allow to run in over 1-2 hours. Subsequent dosing based on TDM.
There is currently no consensus about the dosage for full-term neonates and premature infants. Studies into this are ongoing and when more is known, the dosage will be adjusted in line with the results of the research.
Initial dose:
60
mg/kg/day
in 4
doses. Max: 4 g/day.
Allow to run in over 1-2 hours. ALTERNATIVE:per continuous infusion. Subsequent dosing guided by TDM
Initial dose:
60
mg/kg/day
in 4
doses. Max: 4 g/day.
Allow to run in over 1-2 hours. Subsequent dosing guided by TDM.
Perioperative prophylaxis and prophylaxis of endocarditis in hypersensitivity to penicillin or treatment with penicillin in the 7 days before the procedure
Sampling: first sample at steady state ( 24-48 hours after start of therapy or after 4 doses in patients with adequate renal function)
Target concentration: 10-15 mg/l; target: AUC/MIC ≥ 400 at MIC ≤ 1 mg/L
Renal impaiment in children > 3 months
GFR
Initial dose
Subsequent dosing
50-80 ml/min/1.73 m2
15 mg/kg/dose every 8 hours
Guided by TDM TDM. Consult local protocol (General instruction: determine peak and trough concentration within 24 hours of first dose)
30-50 ml/min/1.73 m2
15 mg/kg/dose every 8-12 hours
Op geleide van TDM. Raadpleeg lokaal protocol (General instruction: determine peak and trough concentration within 24 hours of first dose)
10-30 ml/min/1.73 m2
15 mg/kg/dose every 12-24 hours
Op geleide van TDM. Raadpleeg lokaal protocol General instruction: determine a peak concentration after the first dose and trough concentration before the 2nd dose
<10 ml/min/1.73 m2
15 mg/kg/dose every 24 hours
Op geleide van TDM. Raadpleeg lokaal protocol (General instruction: determine a peak concentration after the first dose and trough concentration before the 2nd dose)
Hemodialyse
15 mg/kg/dose after dialysis
Op geleide van TDM. Raadpleeg lokaal protocol General instruction: determine a peak concentration after the first dose and second concentration within 24 hours)
Le 2014; Zhang 2016; Smit 2021; Chung 2021.
The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here
Side effects in children
Thrombocytopenia, neutropenia, phlebitis, skin conditions, ototoxicity, DRESS syndrome, nephrotoxicity. ‘Red man syndrome’ (RMS) occurs commonly in children (approx. 14%). Risk factors are: age > 2 years, having previously had RMS, vancomycin dose ≥ 10 mg/kg, vancomycin concentration: ≥ 5 mg/ml and previous use of antihistamines. Trough levels up to 20 µg/ml do not give an elevated risk of nephrotoxicity compared to trough levels up to 15 µg/ml. Risk factors for nephrotoxicity occurring are a greater length of treatment, the use of vasopressors and the use of AV-ECMO.
The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here
Contra-indications
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
Warnings & precautions in children
Inflow rate 1-2 hours. ‘Red man syndrome’ can occur if the drug is administered too quickly. Determine the creatinine at least twice a week. Extra checks in premature infants/children because of the immaturity of the kidneys. Using vancomycin present a risk of colonization occurring with ESBL-producing Klebsiella in the gastrointestinal tracts of neonates. Concomitant use with anaesthetics in children linked to erythema and anaphylactoid responses. If administration of vancomycin is needed as surgical prophylaxis, it is recommended that the anaesthetic should be administered after completion of the vancomycin infusion. Note: children who are obese or overweight are more likely to develop elevated levels.
If patients do not achieve the desired serum concentration on intermittent intravenous (IIV) therapy, switching them to continuous intravenous (CIV) therapy is an option. Note: the total daily dose of vancomycin is lower for CIV than for IIV.
Interactions
The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
Frymoyer A et al., Prediction of vancomycin pharmacodynamics in children with invasive methicillin-resistant Staphylococcus aureus infections: a Monte Carlo simulation. , Clin Ther, 2010, Mar;32(3), 534-42
Vella-Brincat et al, Are gentamicin and/or vancomycin associated with ototoxicity in the neonate? A retrospective audit., Neonatology., 2011, 100(2), 186-93
Ofek-Shlomai N et al, Gastrointestinal colonization with ESBL-producing Klebsiella in preterm babies--is vancomycin to blame?, J Clin Microbiol Infect Dis, 2012, Apr;31(4), 567-70
Myers AL et al, Defining risk factors for red man syndrome in children and adults., Pediatr Infect Dis J. , 2012, May;31(5), 464-8
Fung L., Continuous infusion vancomycin for treatment of methicillin-resistant Staphylococcus aureus in cystic fibrosis patients., Ann Pharmacother, 2012, Oct;46(10):, e26
Kitcharoensakkul et al, Vancomycin-induced DRESS with evidence of T-cell activation in a 22-month-old patient. , Allergy Asthma Immunol, 2012, Oct;109(4), 280-1
McKamy et al, Evaluation of a pediatric continuous-infusion vancomycin therapy guideline, Am J Health Syst Pharm, 2012, Dec 1;69(23), 2066-71
Jacqz-Aigrain E et al. , Use of antibacterial agents in the neonate: 50 years of experience with vancomycin administration. , Semin Fetal Neonatal Med, 2013, Feb;18(1), 28-34
Le J et al, Improved vancomycin dosing in children using area under the curve exposure., Pediatr Infect Dis J., 2013, Apr;32(4)
Cies et al, Nephrotoxicity in Patients with Vancomycin Trough Concentrations of 1520 ?g/ml in a Pediatric Intensive Care Unit, Pharmacotherapy., 2013, Apr;33(4), 392-400
Linder N et al. , Duration of vancomycin treatment for coagulase-negative Staphylococcus sepsis in very low birth weight infants. , J Clin Pharmacol, 2013, Jul;76(1), 58-64
Madigan T et al., The effect of age and weight on vancomycin serum trough concentrations in pediatric patients., Pharmacotherapy., 2013, Dec;33(12), 1264-72
Heble DE Jr et al , Vancomycin trough concentrations in overweight or obese pediatric patients., Pharmacotherapy, 2013, Dec;33(12), 1273-7
Cole TS et al , Vancomycin dosing in children: what is the question?, Arch Dis Child, 2013, Dec;98(12), 994-7
Nederlandse Vereniging voor Neurologie , Richtlijn Bacteriele Meningitis, 2013
NVZA, Richtlijn TDM Vancomycine , mei 2014
ErasmusMC-Sophia, protocol Vancomycine , juli 2014
Janssen, E. et al., Towards Rational Dosing Algorithms for Vancomycin in Neonates and Infants Based on Population Pharmacokinetic Modeling, Antimicrob Agents Chemother, 2015, Dec 7;60(2), 1013-21
Ingrande, J, et al., Pharmacokinetics of cefazolin and vancomycin in infants undergoing open-heart surgery with cardiopulmonary bypass, Anesth Analg, 2019, 128(5), 935-943
Noridem, SmPC Vancomycin Noridem 500 mg Plv. f. e. Konz. z. Herst. e. Inflsg. (1-30789), https://www.univadis.at/, 01/2018
Astro, SmPC Vancocin 500 mg Plv. f. e. Konz. z. Herst. e. Inflsg. + e. Lsg. z. Einn. (17126), https://www.univadis.at/, 12/2018
Zhang H, et al., Pharmacokinetic Characteristics and Clinical Outcomes of Vancomycin in Young Children With Various Degrees of Renal Function., J Clin Pharmacol. , 2016, 56(6), 740-8
Chung E, et al., Pharmacokinetics of Vancomycin in Pediatric Patients Receiving Intermittent Hemodialysis or Hemodiafiltration., Kidney Int Rep, 2021, 6(4), 1003-14
Le J, et al., Population-Based Pharmacokinetic Modeling of Vancomycin in Children with Renal Insufficiency., J Pharmacol Clin Toxicol. , 2014, 2(1):, 1017-26
Smit C, et al. , Dosing Recommendations for Vancomycin in Children and Adolescents with Varying Levels of Obesity and Renal Dysfunction: a Population Pharmacokinetic Study in 1892 Children Aged 1-18 Years., Aaps j., 2021, 23(3):, 53