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Premarket Safety and Efficacy Studies for ADHD Medications in Children

Overview of attention for article published in PLOS ONE, July 2014
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Title
Premarket Safety and Efficacy Studies for ADHD Medications in Children
Published in
PLOS ONE, July 2014
DOI 10.1371/journal.pone.0102249
Pubmed ID
Authors

Florence T. Bourgeois, Jeong Min Kim, Kenneth D. Mandl

Abstract

Attention-deficit hyperactivity disorder (ADHD) is a chronic condition and pharmacotherapy is the mainstay of treatment, with a variety of ADHD medications available to patients. However, it is unclear to what extent the long-term safety and efficacy of ADHD drugs have been evaluated prior to their market authorization. We aimed to quantify the number of participants studied and their length of exposure in ADHD drug trials prior to marketing.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 60 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Spain 1 2%
United States 1 2%
Netherlands 1 2%
Germany 1 2%
Unknown 56 93%

Demographic breakdown

Readers by professional status Count As %
Student > Master 11 18%
Other 7 12%
Student > Ph. D. Student 7 12%
Professor > Associate Professor 6 10%
Student > Doctoral Student 5 8%
Other 15 25%
Unknown 9 15%
Readers by discipline Count As %
Medicine and Dentistry 16 27%
Psychology 12 20%
Computer Science 4 7%
Nursing and Health Professions 3 5%
Pharmacology, Toxicology and Pharmaceutical Science 3 5%
Other 10 17%
Unknown 12 20%