2008
DOI: 10.1002/hup.932
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Adverse events in children and adolescents treated with antipsychotic medications

Abstract: Pediatric exposure to antipsychotic polypharmacotherapy confers a higher risk of developing adverse events than monotherapy, especially for females.

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Cited by 68 publications
(61 citation statements)
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References 14 publications
(24 reference statements)
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“…Research has shown an association of APP with increased adverse effects, including extrapyramidal effects, [11][12][13] hyperprolactinemia, [14][15][16] sexual dysfunction, 17 hypersalivation, 18 sedation, 14 cognitive impairment, 19 and diabetes. 20,21 Possible increased risk of sudden cardiac death 22 and mortality 23,24 has been suggested. Additional concerns include drugdrug interactions, problems in determining cause and effect of different treatments, complex drug regimens resulting in decreased compliance, and greater cost.…”
Section: Introductionmentioning
confidence: 99%
“…Research has shown an association of APP with increased adverse effects, including extrapyramidal effects, [11][12][13] hyperprolactinemia, [14][15][16] sexual dysfunction, 17 hypersalivation, 18 sedation, 14 cognitive impairment, 19 and diabetes. 20,21 Possible increased risk of sudden cardiac death 22 and mortality 23,24 has been suggested. Additional concerns include drugdrug interactions, problems in determining cause and effect of different treatments, complex drug regimens resulting in decreased compliance, and greater cost.…”
Section: Introductionmentioning
confidence: 99%
“…[6][7][8][9] The incidence of T1DM varies with geography, age, gender, family history, and race. Risk for developing T1DM in childhood seems to increase with distance from the equator.…”
mentioning
confidence: 99%
“…One factor that can mediate this influence may be time of exposure. Children and adolescents with lengthy exposure to antipsychotic pharmacotherapy were at higher risk of developing neurological, nervous, and/or sensory conditions than were those taking antipsychotic medications for 5 months or less (Jerrell & McIntyre, 2008). Nevertheless, in general, AAs are better tolerated and show improved medication compliance than do TAs (Chakos, Lieberman, Hoffman, Bradford, & Sheitman, 2001).…”
Section: Adverse Impacts Of Typical and Aasmentioning
confidence: 94%