Pharmacokinetics in children
The kinetic parameters of clobazam in 414 children and adults were investigated In a study [Bun 1990]. The kinetic parameters may have been influenced by co-administration of other drugs.
Volume of distribution 194 l,
Clearance 10.17 l / h,
t½ 16 hours and t½ metabolite 15 hours.
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
| Short-term treatment of sudden extreme insomnia |
- Oral
-
2 years
up to
15 years
-
5
- 15
mg/day
in 1
- 2
doses.
-
15 years
up to
18 years
|
| Epilepsy |
- Oral
-
1 month
up to
16 years
-
16 years
up to
18 years
|
| Febrile convulsions |
- Oral
-
6 months
up to
6 years
-
0.5
mg/kg/day
in 1
- 2
doses. Max: 40 mg/day.
- Duration of treatment:
From the moment the fever starts and throughout the entire period with fever
Limited studies have been carried out into the use of clobazam in febrile convulsions. The dose recommendations are based on the experience of experts.
|
Renal impaiment in children > 3 months
GFR ≥10 ml/min/1.73m2: Dose adjustment not required.
GFR <10 ml/min/1.73m2: A general recommendation on dose adjustment cannot be provided.
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
Sleepiness, ataxia, behavioural disorders, sedation, drooling, agitation. Particularly at high doses, in children: paradoxical reactions such as acute excitement and changes in the mental condition.
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
Do not suddenly stop long-term treatment, but instead gradually reduce the dose to prevent withdrawal symptoms.
Effectiveness and side-effects are correlated to CYP2C19 activity (the N-clobazam concentration increases with poor metabolizers)
Interactions
The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
ANXIOLYTICS
This pages provides a list of drugs from the same ATC class for comparison. This does not necessarily mean that these drugs are interchangeable.
| Benzodiazepine derivatives |
|
|
|
N05BA12
|
|
|
|
N05BA08
|
|
|
|
N05BA01
|
|
|
|
N05BA06
|
|
|
|
N05BA04
|
| Diphenylmethane derivatives |
|
|
|
N05BB01
|
| Azaspirodecanedione derivatives |
|
|
|
N05BE01
|
References
-
Bun H, et al, Effects of age and antiepileptic drugs on plasma levels and kinetics of clobazam and N-desmethylclobazam., Pharmacol Toxicol., 1990, Aug;67(2), 136-4
-
Kalra V, et al, Clobazam in refractory childhood epilepsy, Indian J Pediatr, 2010, Mar;77(3), 263-6
-
Canadian Study Group for Childhood Epilepsy, Clobazam has equivalent efficacy to carbamazepine and phenytoin as monotherapy for childhood epilepsy , Epilepsia, 1998, Sep;39(9), 952-9
-
Conry JA, et al, Clobazam in the treatment of Lennox-Gastaut syndrome, Epilepsia, 2009, May;50(5), 1158-66
-
Kaushal S, et al, Safety and efficacy of clobazam versus phenytoin-sodium in the antiepileptic drug treatment of solitary cysticercus granulomas, Neurol India, 2006, Jun;54(2), 157-60
-
Rose W, et al, Intermittent clobazam therapy in febrile seizures, Indian J Pediatr, 2005, Jan;72(1), 31-3
-
Canadian Clobazam Cooperative Group, Clobazam in treatment of refractory epilepsy: the Canadian experience. A retrospective study. , Epilepsia, 1991, May-Jun;32(3):, 407-16
-
Shimizu H, et al, Antiepileptic effects of clobazam in children. , Brain Dev, 1982, 4(1), 57-62
-
Keene DL, et al, Clobazam as an add-on drug in the treatment of refractory epilepsy of childhood, Can J Neurol Sci., 1990, Aug;17(3), 317-9
-
Koeppen D. , Review of clinical studies on clobazam. , Br J Clin Pharmacol. , 1979, 7, Suppl 1139S-50S
-
Seo T, et al, Impact of CYP2C19 polymorphisms on the efficacy of clobazam therapy, Pharmacogenomics, 2008, May;9(5), 527-3
-
Sanofi-Aventis Netherlands BV, SPC Frisium (RVG 09600) mei 2018, www.geneesmiddeleninformatiebank.nl
-
Khosroshahi, N. et al, Diazepam versus clobazam for intermittent prophylaxis of febrile seizures, Indian J Pediatr, 2011, 78(1), 38-40
-
Ng, Y.T. et al, Randomized, phase III study results of clobazam in Lennox-Gastaut syndrome, Neurology, 2011, 77(15), 1473-81
-
Samanta, D. et al, Absence status after starting clobazam in a patient with syndrome of continuous spike and wave during slow sleep (CSWS)., Neurol India, 2014, 62(2), 685-7
-
Sattar, S. et al, Intermittent prophylaxis of recurrent febrile seizures with clobazam versus diazepam, Mymensingh Med, 2014, 23(4), 676-85
-
Incecik, F. et al, Unusual side effects due to clobazam: a case report with edema of the extremities, Acta Neurol Belg, 2018, 118(3), 521-522
-
Koeppen D., Review of clinical studies on clobazam., Br J Clin Pharmacol., 1979, 7, Suppl 1139S-50S
-
Canadian Study Group for Childhood Epilepsy, Clobazam has equivalent efficacy to carbamazepine and phenytoin as monotherapy for childhood epilepsy, Epilepsia, 1998, Sep;39(9), 952-9
-
Canadian Clobazam Cooperative Group, Clobazam in treatment of refractory epilepsy: the Canadian experience. A retrospective study., Epilepsia, 1991, May-Jun;32(3):, 407-16
-
Shimizu H, et al, Antiepileptic effects of clobazam in children., Brain Dev, 1982, 4(1), 57-62
Therapeutic Drug Monitoring
Overdose