The study was carried out in accordance with the guidelines of the Declaration of Helsinki, and the research protocol was approved by the Institutional Review Board of Metro Hospital, Anyang, Republic of Korea. After overnight fasting, the subjects were administered a single oral dose of 20 mg atomoxetine (Strattera®, Eli Lilly and Co., Seoul, Republic of Korea) with 200 mL of water. Blood samples were collected before treatment and at 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 10, 12, and 24 hours after treatment. The blood samples were promptly centrifuged after collection. Plasma samples were kept at −70 °C until analysis.
Strattera
Manufactured by Eli Lilly
Strattera is a laboratory equipment product manufactured by Eli Lilly. It is designed to perform specific functions in a research or analytical setting. The core function of Strattera is to provide precise and reliable measurements or data analysis, supporting various scientific applications.
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Lab products found in correlation
2 protocols using strattera
1
Pharmacokinetics of Atomoxetine in Fasted Subjects
2
Atomoxetine for Intensive UE Motor Training
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The initial recommended and safe dose of atomoxetine (Strattera, by Eli Lilly) in subjects over 70 kg is 40 mg/day; therefore this dose was administered in this study (Simpson & Perry, 2003 ), for the intervention group. Placebo capsules were identical to atomoxetine capsules. Drug condition (ie, real versus placebo) was the only independent variable. In each intervention session (10 total sessions), dosing occurred just prior to intensive, task-oriented UE motor training.
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