2010
DOI: 10.1055/s-0029-1223511
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Risperidonintoxikation bei genetischer Disposition als „poor [non]metabolizer”

Abstract: In intoxications with psychoactive agents, the presence of an enzyme defect in the P450 system should be considered as an additional possible cause.

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Cited by 3 publications
(4 citation statements)
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“…Pimozide is equally effective in other psychotic syndromes, but is currently rarely used because of cardiac toxicity. Similarly, all antipsychotic medications are effective in DD treatment, though tolerability and, thus, adherence differ [ 36 , 37 , 38 , 39 , 40 , 41 , 42 , 43 , 44 , 45 , 46 , 47 , 48 , 49 , 50 , 51 , 52 , 53 , 54 , 55 , 56 ]. The mechanism of action is generally attributable to action on dopamine and serotonin pathways, though other neurotransmitters may also be involved.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Pimozide is equally effective in other psychotic syndromes, but is currently rarely used because of cardiac toxicity. Similarly, all antipsychotic medications are effective in DD treatment, though tolerability and, thus, adherence differ [ 36 , 37 , 38 , 39 , 40 , 41 , 42 , 43 , 44 , 45 , 46 , 47 , 48 , 49 , 50 , 51 , 52 , 53 , 54 , 55 , 56 ]. The mechanism of action is generally attributable to action on dopamine and serotonin pathways, though other neurotransmitters may also be involved.…”
Section: Discussionmentioning
confidence: 99%
“…This drug is chiefly metabolized by CYP2D6. A case report by Strauss and collaborators rightly highlighted the relevance of genetic variants of CYP2D6 when treating DD with risperidone [ 38 ]. The patient was a 37-year-old woman who was a poor metabolizer of risperidone, and in whom a very low dose proved toxic.…”
Section: Use Of Second-generation Antipsychotics In the Treatment Of ...mentioning
confidence: 99%
“…Strauss and collaborators reported the case of a 37-year-old woman with DD treated with risperidone [ 106 ]. High plasma levels suggest a potential metabolic disorder, particularly an unusual genetic polymorphism in the CYP2D6 gene.…”
Section: Collaboration With Pharmacologistsmentioning
confidence: 99%
“…Nebenwirkungen bei Gabe von 300 mg / d Venlafaxin) kein Hinweis. Polymorphismen bei CYP 2D6 mit einer resultierenden verminderten Aktivität treten bei 5-8 % der mitteleuropäischen Bevölkerung auf und können selbst bei geringer Dosierung von Pharmaka, die Substrat von 2D6 sind, mit heftigen Intoxikationssymptomen einhergehen [11]. Über CYP 2D6 läuft ein Abbauweg von Venlafaxin, der andere über CYP 3A4.…”
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