Pharmacokinetics in children
No information
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
| Mucous membrane bleeding with a blood clotting disorder |
- Oral
-
0 years
up to
18 years
and
<
40 kg
-
0 years
up to
18 years
and
≥ 40 kg
-
3
- 4
g/day
in 3
- 4
doses.
- Duration of treatment:
7-10 days
- Intravenous
-
0 years
up to
18 years
-
25
mg/kg/day
in 3
- 4
doses.
- Duration of treatment:
7-10 days
|
| Massive bleeding in case of trauma |
- Intravenous
-
1 month
up to
18 years
- Initial dose:
15
mg/kg/dose,
bolus in 10 minutes. Max: 1 g/dose.
- Maintenance dose:
in continued massive bleeding
2
mg/kg/hour,
continuous infusion over 8 hours or until bleeding stops.
-
Term neonate
- Initial dose:
15
mg/kg/dose,
bolus in 10 minutes. Max: 1 g/dose.
- Maintenance dose:
2
mg/kg/hour,
continuous infusion over 8 hours or until bleeding stops.
|
Renal impaiment in children > 3 months
Oral
- GFR ≥ 50: no dosage adjustment is needed
- GFR 30-50: 100% of normal reversal dose, interval between 2 doses: 12 hours.
- GFR 10-30: 100% of normal reversal dose, interval between 2 doses: 24 hours.
- GFR <10: general advice is not given.
Intravenous
- GFR ≥ 50: no dosage adjustment is needed
- GFR 30-50: 67% of normal reversal dose, interval between 2 doses: 12 hours.
- GFR 10-30: 67% of normal reversal dose, interval between 2 doses: 24 hours.
- GFR <10: general advice is not given.
Clinical consequences
With impaired renal function, the half-life of tranexamic acid may be prolonged. This increases the risk of adverse reactions.
Clinical Effects:
Possible symptoms of overdose include nausea, diarrhea, dizziness, headache, hypotension, and myopathy.
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
Abdominal pain and diarrhoea. These side effects are dose-dependent.
The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here
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
Adjust the dose in renal insufficiency.
Interactions
The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
ANTIFIBRINOLYTICS
This pages provides a list of drugs from the same ATC class for comparison. This does not necessarily mean that these drugs are interchangeable.
References
-
Rademaker C.M.A. et al, Geneesmiddelen-Formularium voor Kinderen, 2007
-
Nederlandse Vereniging van Hemofiliebehandelaars (NVHB)., Richtlijn Diagnostiek en Behandeling van Hemofilie, 2020
-
NVK, Werkboek kinderhematologie, www.hematologienederland.nl, 23 sept 2012
-
MMI, Online GL, Cyklokapron®, Filmtbl., Accessed June 7, 2018.
-
MEDA, SmPC Cyklokapron 500mg Filmtabletten (6376142.00.00), 07/2016
-
Pfizer, SmPC Cyklokapron 500mg/5ml_1000mg/10ml Injektionslösung (6376165.00.00), 06/2016
-
Carino, SmPC Tranexamsäure 100mg/ml Injektionslösung (88847.00.00), 08/2014
-
Turner, NM. Leroy, P., Advanced Paediatric Life Support, de Nederlandse editie, 2017, 5e editie
-
NKFK Workinggroup Acute Kidney Impairment, Extrapolation of KNMP risk analysis "Impaired renal function" for adults to children, 20 Dec 2021
-
Beno S,et al, Tranexamic acid in pediatric trauma: why not?, Crit Care, 2014, Jul 2;18(4):, 313.
-
Beno S,et al, Tranexamic acid in pediatric trauma: why not?, Crit Care, 2014, Jul 2;18(4):, 313.
Therapeutic Drug Monitoring
Overdose