Pharmacokinetics in children
No information is present at this moment.
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
| Prophylaxis for thromboembolic complications |
- Subcutaneous
-
0 months
up to
2 months
[3]
[12]
-
1.5
mg/kg/day
in 2
doses. (equivalent to 150 IU/kg/day).
- Titrate the dose based on the concentrations, see warning & precautions section
- Dissolve the dose in a minimum of 0.2 ml
-
2 months
up to
18 years
[3]
[12]
-
1
mg/kg/day
in 2
doses. (equivalent to 100 IU/kg/day).
- Titrate the dose based on the concentrations, see warnings & precautions section
- Dissolve the dose in a minimum of 0.2 ml
|
| Deep vein thrombosis |
- Subcutaneous
-
Premature neonates:
Gestational age
<
37 weeks
[3]
-
4
mg/kg/day
in 2
doses. (equivalent to 400 IU/kg/day).
- Titrate the dose based on the concentrations, see warnings & precautions section
- The dose may be diluted to a mimumum of 0,2 ml to enable precise administration of small doses.
-
0 months
up to
2 months
[3]
-
3.4
mg/kg/day
in 2
doses. (equivalent to 340 IU/kg/day).
- Titrate the dose based on the concentrations, see warnings & precautions section
- The dose may be diluted to a mimumum of 0,2 ml to enable precise administration of small doses.
-
2 months
up to
6 years
[1]
[3]
-
2.6
mg/kg/day
in 2
doses. (equivalent to 260 IU/kg/day).
- Titrate the dose based on the concentrations, see warnings & precautions section
- The dose may be diluted to a mimumum of 0,2 ml to enable precise administration of small doses.
-
6 years
up to
18 years
[3]
-
2
mg/kg/day
in 2
doses. (equivalent to 200 IU/kg/day).
- Titrate the dose based on the concentrations, see warnings & precautions section
- The dose may be diluted to a mimumum of 0,2 ml to enable precise administration of small doses.
|
Renal impaiment in children > 3 months
Therapeutic dose:
- GFR ≥ 50: adjustment of dose is not necessary.
- GFR 30-50: 1st dose 100% of normal single dose, then 75% of normal single dose, interval between two doses: 12 hours; if used longer than 3 days, dose according to anti-Xa levels.
- GFR 10-30: 1st dose 100% of normal single dose, then 50% of normal single dose, interval between doses: 12 hours; if used for more than 3 days, dose according to anti-Xa levels.
- GFR <10: general advice is not given.
Prophylactic dose:
- GFR ≥10: adjustment of dose is not necessary.
- GFR <10: general advice is not given.
Clinical consequences
With impaired kidney function, the half-life of enoxaparin is prolonged. This increases the risk of bleeding.
Clinical implications:
Bleeding
The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here
Side effects
No information is present at this moment.
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
1 mg of protamine sulfate neutralizes 100 IU of anti-Xa-enoxaparin. See further protamine monograph.
Target levels and monitoring:
Anti-FXa level measured 4 hours after gift (3 hours in neonates); first anti-FXa measured after 3 gifts.
Target anti-FXa level:
therapeutic: 0.5 - 1.0 E/mL;
prophylactic: 0.1 - 0.4 E/mL,
>40 kg: generally no monitoring anti-FXa necessary, WELL in sick children, co-medication and/or poor renal function
After any dose adjustment it is not necessary to wait for 3 doses and can be agreed upon with the local laboratory. Upon reaching therapeutic level, only further monitoring is necessary in neonates, critically ill patients, and patients during asparaginase use (due to decreasing antithrombin).
Interactions
The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
ANTITHROMBOTIC AGENTS
This pages provides a list of drugs from the same ATC class for comparison. This does not necessarily mean that these drugs are interchangeable.
| Heparin group |
|
|
|
B01AB04
|
|
|
|
B01AB01
|
|
|
|
B01AB06
|
| Platelet aggregation inhibitors excl. heparin |
|
|
|
B01AC06
|
References
-
NVK, Werkboek kinderhematologie, http://www.hematologienederland.nl/werkboek-kinderhematologie , 2014, Geraadpleegd 20-01-14
-
M. Cnossen. , Expertopinie profylaxe dosering sectie Benigne Hematologie, 14 jan 2014
-
Klaassen ILM. et al, Are low-molecular-weight heparins safe and effective in children? A systematic review., Blood Rev, 2018, 10.1016/j.blre.2018.06.003
-
Sanofi-Aventis Deutschland GmbH, SmPC, Clexane® Injektionslösung in einer Fertigspritze (15854.00.00), 04/18
-
Techdow Europe AB, SmPC, Inhixa Injektionslösung (EU/1/16/1132/001), 08/17
-
Sanofi-Aventis Deutschland GmbH, SmPC, Clexane® multidose Injektionslösung (99843.00.00), 04/18
-
Laboratorios Farmacéuticos ROVI, SmPC, Enoxaparin Becat Injektionslösung in einer Fertigspritze (99912.00.00), 03/18
-
Chemi S.p.A, SmPC, Hepaxane Injektionslösung in einer Fertigspritze (2201226.00.00), 10/18
-
Uptodate: UpToDate®, Pediatric Drug information: Enoxaparin Topic 13270 Version 181.0, accessed 03/19
-
DinH C, et al, A Critical Evaluation of Enoxaparin Dose Adjustment Guidelines in Children, J Pediatr Pharmacol Ther, 2019, 24(2):, 128–133
-
NKFK Workinggroup Acute Kidney Impairment, Extrapolation of KNMP risk analysis "Impaired renal function" for adults to children, 20 Dec 2021
-
Monagle P, et al., Antithrombotic therapy in neonates and children: Antithrombotic Therapy and Prevention of Thrombosis. 9th ed: American College of Chest Physicians Evid ence-Based Clinical Practice Guidelines., Chest, 2012, Feb;141(2 Suppl), e737S-e801S
Therapeutic Drug Monitoring
Overdose