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FDA Approves Strattera(R) for Maintenance of ADHD in Children and Adolescents
Date:5/9/2008

u or your child takes, including vitamins, and herbal supplements. Do not start any new medicine while taking STRATTERA without talking to your doctor first.

Tell your doctor if you or your child is pregnant, planning to become pregnant, or breastfeeding.

In children, the most common side effects were upset stomach, decreased appetite, nausea or vomiting, tiredness, and drowsiness. In adults, the most common side effects were constipation, dry mouth, nausea, decreased appetite, dizziness, problems sleeping, sexual side effects, problems urinating, and menstrual cramps. Most people in clinical studies who experienced side effects were not bothered enough to stop using Strattera. Strattera has not been tested in children under 6 years of age or in geriatric adults.

For Medication Guide, visit http://www.Strattera.com.

For full Prescribing Information, including Boxed Warning information, visit http://www.Strattera.com/.

About Eli Lilly and Company

Lilly, a leading innovation-driven corporation, is developing a growing portfolio of first-in-class and best-in-class pharmaceutical products by applying the latest research from its own worldwide laboratories and from collaborations with eminent scientific organizations. Headquartered in Indianapolis, Ind., Lilly provides answers - through medicines and information -- for some of the world's most urgent medical needs. Additional information about Lilly is available at http://www.lilly.com.

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This press release contains forward-looking statements about Strattera for the treatment of ADHD and reflects Lilly's current beliefs. However, as with any pharmaceutical product, there are substantial risks and uncertainties in the process of development and commercialization, including the risk of side effects and other sa
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SOURCE Eli Lilly and Company
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