Some include a decrease in appetite, weight loss, nausea, vomiting, dizziness, and insomnia. Lisdexamfetamine and atomoxetine have a number of side effects in common. Medscape - Attention deficit hyperactivity disorder (ADHD)-specific dosing for Strattera (atomoxetine), frequency-based adverse effects, comprehensive interactions, contraindications, pregnancy & lactation schedules, and cost information. withdrawal symptoms in newborns. Applies to the following strengths: 10 mg; 25 mg; 40 mg; 18 mg; 60 mg; 80 mg; 100 mg-Mild Liver Dysfunction (Child-Pugh A): No adjustment recommended.Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.The easiest way to lookup drug information, identify pills, check interactions and set up your own personal medication records. Rare cases of liver failure have also been reported, including a case that resulted in a liver transplant. You may report side effects to FDA at 1-800-FDA-1088.Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. There have been postmarketing reports of anxiety In a randomized, double-blind, placebo-controlled, abuse-potential study in adults comparing effects of Atomoxetine and placebo, Atomoxetine was not associated with a pattern of response that suggested stimulant or euphoriant properties.Clinical study data in over 2000 children, adolescents, and adults with ADHD and over 1200 adults with depression showed only isolated incidents of drug diversion or inappropriate self-administration associated with Atomoxetine. It may harm them.This Medication Guide summarizes the most important information about Atomoxetine capsules.

Symptoms of ADHD in teens include inattention, hyperactivity/impulsivity, or a combination of these. The following drugs have been reported to interact with atomoxetine. Although this is not conclusive evidence that Atomoxetine causes aggressive behavior or hostility, these behaviors were more frequently observed in clinical trials among children, adolescents, and adults treated with Atomoxetine compared to placebo.Although uncommon, allergic reactions, including anaphylactic reactions, angioneurotic edema, urticaria, and rash, have been reported in patients taking Atomoxetine.In adult ADHD controlled trials, the rates of urinary retention (1.7%, 9/540) and urinary hesitation (5.6%, 30/540) were increased among Atomoxetine subjects compared with placebo subjects (0%, 0/402; 0.5%, 2/402, respectively). The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for Atomoxetine and any potential adverse effects on the breastfed child from Atomoxetine or from the underlying maternal condition.Anyone considering the use of Atomoxetine in a child or adolescent must balance the potential risks with the clinical need The pharmacokinetics of Atomoxetine in children and adolescents are similar to those in adults. Again, a doctor will decide if the benefits outweigh the risks . ADHD symptoms were statistically significantly improved on Atomoxetine compared with placebo, as measured on the ADHDRS scale. Adderall or Dexedrine because of its slow, measured absorption by the body When remedial measures alone are insufficient, the decision to prescribe drug treatment medication will depend upon the physician’s assessment of the chronicity and severity of the patient’s symptoms.The total daily dose in children and adolescents should not exceed 1.4 mg/kg or 100 mg, whichever is less.The maximum recommended total daily dose in children and adolescents over 70 kg and adults is 100 mg.It is generally agreed that pharmacological treatment of ADHD may be needed for extended periods.

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