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Shire to Present Important Study Findings on its ADHD Treatments at a Major Psychiatric Meeting on October 29 and 30
Date:10/29/2009

ansdermal system) CII

October 30, 2009; 3:00 pm to 5:30 pm ET / 9:00 am to 11:30 am HT

Pharmacokinetics of Methylphenidate Transdermal System and Osmotic-Release Oral System Methylphenidate in Children and Adolescents With ADHD

Poster Presentation # 4.52

October 30, 2009; 3:00 pm to 5:30 pm ET / 9:00 am to 11:30 am HT

Pharmacokinetic Predictors of Abuse-Related Liking With Transdermal and Subcutaneous Methylphenidate

Poster Presentation # 4.54

October 30, 2009; 3:00 pm to 5:30 pm ET / 9:00 am to 11:30 am HT

Evaluation of the Tolerability and Effectiveness of the Methylphenidate Transdermal System Over 6 Months in Adolescents With ADHD

Poster Presentation # 4.55

Additional information about INTUNIV and Full Prescribing Information are available at http://www.intuniv.com.

Additional information about Vyvanse and Full Prescribing Information, including the Medication Guide, are available at http://www.vyvanse.com.

Additional information about Daytrana and Full Prescribing Information, including the Medication Guide, are available at http://www.daytrana.com.

INTUNIV IMPORTANT SAFETY INFORMATION

INTUNIV is indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) in children and adolescents aged 6 to 17. Efficacy was established in two controlled clinical trials (8 and 9 weeks in duration). The physician electing to use INTUNIV for extended periods should periodically reevaluate its long-term usefulness for the individual patient.

INTUNIV should not be used in patients with a history of hypersensitivity to gua
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SOURCE Shire plc
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