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Atomoxetine: a novel treatment for child and adult ADHD
Attention deficit hyperactivity disorder (ADHD) is a common chronic condition with childhood onset that can continue into adulthood. Medication is a fundamental element in the management of this disorder. Atomoxetine is the newest nonstimulant medication approved by the United States Food and Drug A...
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Formato: | Texto |
Lenguaje: | English |
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Dove Medical Press
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2671957/ https://www.ncbi.nlm.nih.gov/pubmed/19412494 |
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author | Ledbetter, Marcialee |
author_facet | Ledbetter, Marcialee |
author_sort | Ledbetter, Marcialee |
collection | PubMed |
description | Attention deficit hyperactivity disorder (ADHD) is a common chronic condition with childhood onset that can continue into adulthood. Medication is a fundamental element in the management of this disorder. Atomoxetine is the newest nonstimulant medication approved by the United States Food and Drug Administration (FDA) for the treatment of ADHD. It is the only nonstimulant medication approved by the FDA for treatment of adult ADHD. Atomoxetine is a norepinephrine reuptake inhibitor that selectively inhibits the presynaptic norepinephrine transporter. A growing body of literature supports the use of atomoxetine both in children and adults with ADHD. This paper summarizes information from the literature about atomoxetine, including pharmacokinetics, pharmacodynamics, clinical trials, dosing, and side-effects. |
format | Text |
id | pubmed-2671957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-26719572009-04-30 Atomoxetine: a novel treatment for child and adult ADHD Ledbetter, Marcialee Neuropsychiatr Dis Treat Expert Opinion Attention deficit hyperactivity disorder (ADHD) is a common chronic condition with childhood onset that can continue into adulthood. Medication is a fundamental element in the management of this disorder. Atomoxetine is the newest nonstimulant medication approved by the United States Food and Drug Administration (FDA) for the treatment of ADHD. It is the only nonstimulant medication approved by the FDA for treatment of adult ADHD. Atomoxetine is a norepinephrine reuptake inhibitor that selectively inhibits the presynaptic norepinephrine transporter. A growing body of literature supports the use of atomoxetine both in children and adults with ADHD. This paper summarizes information from the literature about atomoxetine, including pharmacokinetics, pharmacodynamics, clinical trials, dosing, and side-effects. Dove Medical Press 2006-12 /pmc/articles/PMC2671957/ /pubmed/19412494 Text en © 2006 Dove Medical Press Limited. All rights reserved |
spellingShingle | Expert Opinion Ledbetter, Marcialee Atomoxetine: a novel treatment for child and adult ADHD |
title | Atomoxetine: a novel treatment for child and adult ADHD |
title_full | Atomoxetine: a novel treatment for child and adult ADHD |
title_fullStr | Atomoxetine: a novel treatment for child and adult ADHD |
title_full_unstemmed | Atomoxetine: a novel treatment for child and adult ADHD |
title_short | Atomoxetine: a novel treatment for child and adult ADHD |
title_sort | atomoxetine: a novel treatment for child and adult adhd |
topic | Expert Opinion |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2671957/ https://www.ncbi.nlm.nih.gov/pubmed/19412494 |
work_keys_str_mv | AT ledbettermarcialee atomoxetineanoveltreatmentforchildandadultadhd |