In neonates, premature neonates and children, the following kinetic parameters have been found after IV administration (Charles 1997, Huisman-de Boer 1995, Pullen 2006, Pullen 2007, Schaad 1983):
Age
PNA (avg)
n=
t½ (hours)
Cl (l/kg/hour)
Vd (ml/kg)
26-32 weeks GA
3 days
17
6.7 ± 1.7
0.066 ± 0.024
671 ± 117
25-42 (avg. 35) weeks GA
0.8 days
150
5.2 ± 1.9
0.096 ± 0.036
650 ± 130
26-41 (avg. 34) weeks GA
25 days
32
3.0 ± 1.3
0.18 ± 0.10
660 ± 270
2-14.5 years
-
12
1.2 ± 0.06
764 ± 58
The following kinetic parameters have been observed in infants aged over 4 months and in children after oral administration (Ginsburg 1979, Ginsburg 1981, Nelson 1982, Van Niekerk 1985, Schaad 1986):
t½ (hours)
HTmax (hours)
Cl (l/kg/hour)
Vd (l/kg)
Cmax (µg/ml) (15-25 mg/kg)
1.1-1.8
1-1.5
1.16-1.30
1.95-2.17
3.2-8.9
In a pooled popPK study by Keij et al. 2023, absorption of amoxicillin in neonates was estimated to be delayed. Tmax was estimated to be 9 hours. This would lead to a gradually increase in plasma concentration and justify twice daily dosing. Clearance (L/h/kg) in neonates born after 30 weeks’ gestation was found to increase with postnatal age (PNA day 10, 1.25-fold; PNA day 20, 1.43-fold vs PNA day 3). Oral bioavailability was estimated to be 87%. [Keij 2023]
dose recommendation of formulary compared to licensed use (on-label versus off-label)
30-60 minutes before the treatment:
50
mg/kg/dose,
once only.
Max single dose:
2 g/dose.
Endocarditis prophylaxis in hypersensitivity to penicillin or treatment with penicillin in the 7 days before the procedure: - for procedures in the oral cavity and upper respiratory tract: clindamycin (for the dosage, refer to the monograph on clindamycin) - for procedures in the urogenital tract and digestive tract: vancomycin (for the dosage, refer to the monograph on vancomycin)
30-60 minutes before the treatment:
50
mg/kg/dose,
once only.
Max single dose:
2 g/dose.
Endocarditis prophylaxis in hypersensitivity to penicillin or treatment with penicillin in the 7 days before the procedure: - for procedures in the oral cavity and upper respiratory tract: clindamycin (for the dosage, refer to the monograph on clindamycin) - for procedures in the urogenital tract and digestive tract: vancomycin (for the dosage, refer to the monograph on vancomycin)
Early localized and disseminated Lyme disease, with the exception of meningitis and Lyme carditis
100 percentage of single dose and dosing interval : 12 up to 24 uur
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
Superficial tooth discoloration was observed in children using dispersible tablets and oral suspensions. Adequate oral hygiene can help to avoid tooth discolotrations as brushing usually removes them [SmPC].
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
In cases of long-term use, application in premature children or during the neonatal period, check the renal and hepatic function regularly and have regular haematological tests carried out. Cases of nephrotoxicity have been described after using amoxicillin.
Interactions
The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
Pullen J, et al, Amoxicillin pharmacokinetics in (preterm) infants aged 10 to 52 days: effect of postnatal age, Ther Drug Monit., 2007, 29, 376-80
Pullen J, et al, Population pharmacokinetics and dosing of amoxicillin in (pre)term neonates, Ther Drug Monit., 2006, 28, 226-31
Sánchez Navarro A., New formulations of amoxicillin/clavulanic acid: a pharmacokinetic and pharmacodynamic review, Clin Pharmacokinet, 2005, 44, 1097-115
EMA, Amoxicilline: Public Assessment Report for paediatric studies submitted in accordance with Article 45 of Regulation (EC) No1901/2006, www.hma.eu, Geraadpleegd 13 juni 2012, http://www.hma.eu/fileadmin/dateien/Human_Medicines/CMD_h_/Paediatric_Regulation/Assessment_Reports/Article_45_work-sharing/Amoxicillin_2010_07_45PaedPAR.pdf
NVK, Richtlijn Helicobacter Pylori-infectie bij kinderen van 0-18 jaar, 2012
Mrvos R et al, Amoxicillin renal toxicity: how often does it occur?, Pediatr Emerg Care, 2013 , May;29(5):, 641-3
Verduijn MM et al, NHG-Behandelrichtlijn endocarditis profylaxe, www.nhg.org, 2016
Habib G et al, ESC Guidelines for the management of infective endocarditis: The Task Force for the Management of Infective Endocarditis of the European Society of Cardiology (ESC), Eur Heart J, 2015 Nov 21, 36(44), 3075-128
Charles BG et al. , Population pharmacokinetics of intravenous amoxicillin in very low birth weight infants., J Pharm Sci. , 1997 , Nov;86(11), 1288-92
Huisman-de Boer JJ et al., Amoxicillin pharmacokinetics in preterm infants with gestational ages of less than 32 weeks., Antimicrob Agents Chemother., 1995 , Feb;39(2), 431-4
Schaad UB et al. , Single-dose pharmacokinetics of intravenous clavulanic acid with amoxicillin in pediatric patients., Antimicrob Agents Chemother., 1983 , Feb;23(2), 252-5
Ginsburg CM et al., Comparative pharmacokinetics of amoxicillin and ampicillin in infants and children, Pediatrics. , 1979 , Nov;64(5), 627-31
Ginsburg CM et al. , Comparative pharmacokinetics of cyclacillin and amoxicillin in infants and children., Antimicrob Agents Chemother., 1981 , Jun;19(6):, 1086-8
Nelson JD et al. , Pharmacokinetics of potassium clavulanate in combination with amoxicillin in pediatric patients. , Antimicrob Agents Chemother., 1982 , Apr;21(4), 681-2
van Niekerk CH et al. , Pharmacokinetic study of a pediatric formulation of amoxycillin and clavulanic acid in children., Eur J Clin Pharmacol , 1985;, 29, 235-9
Schaad UB et al. , Pharmacokinetics of a syrup formulation of amoxycillin-potassium clavulanate in children. , J Antimicrob Chemother., 1986 , Mar;17(3), 341-5
Sandoz, SmPC Ospamox 250 mg/5 ml Plv. f. orale Susp. (17663), https://www.univadis.at/, 10/2017
Jones N, et al, Joint ESPGHAN/NASPGHAN Guidelines for the Management of Helicobacter pylori in Children and Adolescents (Update 2016), JPGN, 2017, 64, 991-1003
European Committee on Antimicrobial Susceptibility Testing - EUCAST, Clinical breakpoints - breakpoints and guidance, https://www.eucast.org/clinical_breakpoints, Jan2, 2023
Dutch Working Party on Antibiotic Policy (SWAB) - Special Interest Group Pediatrics, Expert opinion on high dosing for infections caused by microorganisms susceptible to increased doses., Dec 6, 2022
Keij FM, et al. , Oral antibiotics for neonatal infections: a systematic review and meta-analysis., J Antimicrob Chemother., 2019, 74(11):, 3150-61
Mir F, et al. , Simplified antibiotic regimens for treatment of clinical severe infection in the outpatient setting when referral is not possible for young infants in Pakistan (Simplified Antibiotic Therapy Trial [SATT]): a randomised, open-label, equivalence trial., Lancet Glob Health, 2017, 5(2):, e177-e85
Keij FM, et al. . 2023., Oral and Intravenous Amoxicillin Dosing Recommendations in Neonates: A Pooled Population Pharmacokinetic Study. , Clin Infect Dis, 2023, Nov 30;77(11), 1595-1603
Mir F, et al., Serum amoxicillin levels in young infants (0-59 days) with sepsis treated with oral amoxicillin., Arch Dis Child, 2020, 105(12), 1208-14
Keij FM, et al., RAIN study: a protocol for a randomised controlled trial evaluating efficacy, safety and cost-effectiveness of intravenous-to-oral antibiotic switch therapy in neonates with a probable bacterial infection., BMJ Open, 2019, 9(7), e026688
Keij FM,et al., Efficacy and safety of switching from intravenous to oral antibiotics (amoxicillin-clavulanic acid) versus a full course of intravenous antibiotics in neonates <.....> , Lancet Child Adolesc Health, 2022, 6(11), 799-809