De volgende kinetische parameters zijn gevonden na een eenmalige dosis van 2,5-5 mg buspiron [Edwards 2006] en bij steady state na tweemaal daagse doses [Salazar 2001]:
| Studie | Edwards 2006 | Salazar 2001 | |||||
| Leeftijd (jaar) | 2-6 | 6-12 | 13-17 | ||||
| n | 20 | 12 | 12 | ||||
| Dosis (mg/d) | 2.5-5 | 15 | 30 | 60 | 15 | 30 | 60 |
| Cmax (ng/ml) | 1,14 ± 0,75 | 0,67 | 1,96 | 3,96 | 0,54 | 1,44 | 2,64 |
| Tmax (uur) | 0,80 ± 0,40 | 1,0 | 1 | 1 | 1 | 1 | 1 |
| t½ (uur) | 1,61 ± 0,32 | 1,99 | 3,13 | 2,70 | 2,90 | 3,44 | 3,37 |
| Cl/F (l/uur/kg) | 87,8 ± 44,8 | - | - | - | - | - | - |
Off-label
Licensed use Licensed useTablet (hydrochloride) 10 mg
| Anxiety disorders |
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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.
At creatinine clearance <10 ml / min, a study in adults found an increased AUC with reduced kidney function, but the t½ did not differ significantly. In another study in adults, no difference in pharmacokinetic parameters was observed with a decrease in renal function. There is a large inter-individual variation in t½. Buspiron is dosed according to the effect and side effects; this is no different with reduced kidney function.
The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here
Abnormal involuntary movements [Buitelaar 1998] and occasional cases of sleep walking and nightmares have been reported [Simeon 1994.] An increase in aggression, agitation and euphoric mania has been reported in psychiatric prepubertal patients with anxiety symptoms and moderate aggressive behavior [Pfeffer 1997].
The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here
Zeer vaak (≥ 10%): duizeligheid en licht gevoel in het hoofd, hoofdpijn, slaperigheid, sufheid.
Vaak (1-10%): nervositeit slapeloosheid, concentratiestoornis, verwardheid, depressie, woede, wazig zien, paresthesieën, coördinatiestoornissen, tremoren, tinnitus, tachycardie, pijn op de borst, hartkloppingen, keelpijn, verstopte neus, faryngolaryngeale pijn, maag-darmstoornissen, hyperhidrose of klamheid, huiduitslag, pijn in spieren en gewrichten, vermoeidheid, zwakte.
Zelden (0,01-0,1%): angioneurotisch oedeem, ecchymose, urticaria, pruritus, alopecia.
Zeer zelden (< 0,01%): hallucinaties, psychose, labiliteit, serotonine syndroom, convulsies, tunnelvisie, extrapiramidale stoornis, tandrad stijfheid, dyskinesie, dystonie, syncope, amnesie, ataxie, parkinsonisme, acathisie, rusteloze benensyndroom, rusteloosheid, urineretentie, galactorroe
The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here
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
No information available on specific warnings and precautions in children.
The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
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 | ||
| N05BA09 | ||
| N05BA01 | ||
| N05BA06 | ||
| N05BA04 | ||
| Diphenylmethane derivatives | ||
|---|---|---|
| N05BB01 | ||