| Literature DB >> 16768642 |
James J McGough1, Keith McBurnett, Oscar Bukstein, Timothy E Wilens, Laurence Greenhill, Marc Lerner, Mark Stein.
Abstract
This 8-week, open-label extension of a double-blind study reports on safety data for 171 adolescents with attention-deficit/hyperactivity disorder (ADHD) who received once-daily OROS methylphenidate (MPH) (18-72 mg/day). Headache, anorexia, and insomnia were the most frequently reported treatment-related adverse events. The incidence of adverse events was not related to dose. OROS MPH was safe and well tolerated at doses up to 72 mg/day.Entities:
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Year: 2006 PMID: 16768642 DOI: 10.1089/cap.2006.16.351
Source DB: PubMed Journal: J Child Adolesc Psychopharmacol ISSN: 1044-5463 Impact factor: 2.576