Rats were treated with 1, 10, or 50 mg/kg/day (approximately 0.2, 2, and 8 times, respectively, the maximum human dose on a mg/mThe safety, efficacy and pharmacokinetics of STRATTERA in geriatric patients have not been evaluated.Atomoxetine exposure (AUC) is increased, compared with normal subjects, in EM subjects with moderate (Child-Pugh Class B) (2-fold increase) and severe (Child-Pugh Class C) (4-fold increase) hepatic insufficiency. Psychoses. Learn about drug imprint, side effects, uses (treating), dosage, interaction, overdose, and warnings. The medicine from inside the capsule can be dangerous if it gets in your eyes.
The capsules are imprinted with edible black ink.STRATTERA is indicated for the treatment of Attention-Deficit/The efficacy of STRATTERA Capsules was established in seven clinical trials in outpatients with ADHD: four 6 to 9-week trials in pediatric patients (ages 6 to 18), two 10-week trial in adults, and one maintenance trial in For the Inattentive Type, at least 6 of the following symptoms must have persisted for at least 6 months: lack of attention to details/careless mistakes, lack of sustained attention, poor listener, failure to follow through on tasks, poor organization, avoids tasks requiring sustained mental effort, loses things, easily distracted, forgetful. You can ask your doctor or pharmacist forinformation about STRATTERA that was written for healthcare professionals. The elimination half-life of 4-hydroxyatomoxetine is similar to that of N-desmethylatomoxetine (6 to 8 hours) in EM subjects, while the half-life of N-desmethylatomoxetine is much longer in PM subjects (34 to 40 hours).Atomoxetine is excreted primarily as 4-hydroxyatomoxetine-O-glucuronide, mainly in the urine (greater than 80% of the dose) and to a lesser extent in the feces (less than 17% of the dose). Labor & delivery. Assess cardiovascular status and do physical exam. Skip the missed dose if it is almost time for your next scheduled dose. It is eliminated primarily by oxidative The pharmacokinetics of atomoxetine have been evaluated in more than 400 children and adolescents in selected clinical trials, primarily using population pharmacokinetic studies. Atomoxetine may also be used for purposes not listed in this medication guide. You may report side effects to FDA at 1-800-FDA-1088.Tell your doctor about all your current medicines and any you start or stop using, especially:a cold or allergy medicine that contains a decongestant such as pseudoephedrine or phenylephrine.This list is not complete. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. Tell your doctor if you are pregnant or plan to become pregnant before taking Strattera.If you are pregnant, your name may be listed on a pregnancy registry to track the effects of atomoxetine on the baby.It may not be safe to breastfeed while using Strattera. Atomoxetine affects chemicals in the brain and nerves that contribute to Atomoxetine may also be used for purposes not listed in this medication guide.Atomoxetine can affect growth in children. Keep a list of your medicines with you to show your doctor and pharmacist.This is not a complete list of possible side effects. Stay alert to changes in your mood or symptoms, especially if you have ever had suicidal thoughts.Do not use Strattera if you have used an MAO inhibitor in the past 14 days. Use atomoxetine regularly to get the most benefit. Although no evidence of liver injury was detected in clinical trials of about 6000 patients, there have been rare cases of clinically significant liver injury that were considered probably or possibly related to STRATTERA use in postmarketing experience. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. For all studies, (including open-label and long-term studies), 6.3% of extensive metabolizer (EM) patients and 11.2% of poor metabolizer (PM) patients discontinued because of an adverse reaction. Substance active: Atomoxetine Titulaire : Lilly France SA Critères d'octroi: TDHA enfants et adolescents après échec des traitements bénéficiant d’une AMM dans l’indication ; TDAH de l’adulte; En l’absence de pathologies cardiovasculaires …
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