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Strattera (Atomoxetine)

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Strattera is a non-stimulant medication used for adults and children with attention-deficit/hyperactivity disorder (ADHD). This medication has a high risk of suicidal thoughts in children and adolescents.

Other names for this medication:
Atomoxetine, Attentrol, Axepta, Tomoxetin

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Also known as: Atomoxetine


Strattera (atomoxetine) affects chemicals in the brain and nerves that contribute to hyperactivity and impulse control.

Strattera is used to treat attention deficit hyperactivity disorder (ADHD).


Usual Adult Dose for Attention Deficit Disorder:

-Initial Dose: 40 mg/day orally. -Maintenance Dose: Increase dose to 80 mg/day orally after a minimum of 3 days at the initial dose. -Maximum Dose: After 2 to 4 additional weeks, the dose may be increased up to 100 mg/day in patients who have not achieved an optimal response. Comments: Take dose once a day in the morning OR as evenly divided doses in the morning and late afternoon/early evening. Use: Treatment of Attention Deficit Hyperactivity Disorder (ADHD).

Usual Pediatric Dose for Attention Deficit Disorder:

70 kg or Less: -Initial Dose: 0.5 mg/kg/day orally. -Maintenance dose: Increase dose to 1.2 mg/kg/day after a minimum of 3 days at the initial dose. -Maximum dose: 1.4 mg/kg/day or 100 mg/day, whichever is less. Over 70 kg: -Initial Dose: 40 mg/day orally. -Maintenance dose: Increase dose to 80 mg/day after a minimum of 3 days at the initial dose. -Maximum dose: After 2 to 4 additional weeks, the dose may be increased up to 100 mg/day in patients who have not achieved an optimal response. Comments: Take dose once a day in the morning OR as evenly divided doses in the morning and late afternoon/early evening. Use: Treatment of Attention Deficit Hyperactivity Disorder (ADHD) in pediatric patients age 6 and older.

Detailed Strattera dosage information


If you overdose Generic Strattera and you don't feel good you should visit your doctor or health care provider immediately.


Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture and heat. Throw away any unused medication after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Strattera are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.


Do not take Strattera if you are allergic to any of Strattera’s components. Do not take Strattera if you're pregnant or you plan to have a baby, or if you are a nursing mother. Do not take Strattera if you are taking or have taken a monoamine oxidase inhibitor (MAOI) (e.g., phenelzine) within the last 14 days. Do not take Strattera if you have certain heart problems (e.g., heart defect, heart failure), certain types of irregular heartbeat, severe blood vessel problems, or narrow-angle glaucoma. Children and teenagers who take Strattera may be at increased risk of suicidal thoughts or actions. Adults may also be affected. The risk may be greater in patients who have had suicidal thoughts or actions in the past. The risk may also be greater in patients who have had bipolar (manic-depression) illness, or if their family members have had it. Watch patients who take Strattera closely. Do not open the capsules or take them apart. Wash your hands immediately after using Strattera. Do not get Strattera in your eye as it may cause irritation. If you get Strattera in your eyes or nose, rinse at once with cool water. Lab tests, including heart rate, blood pressure, and liver function, may be performed while you use Strattera. Use Strattera with caution in the elderly. They may be more sensitive to its effects, especially dizziness. Corticosteroids may affect growth rate in children and teenagers in some cases. They may need regular growth checks while they take Strattera. Strattera should be used with extreme caution in children younger than 6 years old. Safety and effectiveness in these children has not been confirmed. Sit up or stand slowly, especially in the morning. Avoid consuming alcohol while taking Strattera. Avoid driving or operating machinery, as atomoxetine can cause sleepiness or dizziness. Do not stop taking Strattera suddenly.

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Diagnosis of disseminated candidiasis by fine needle aspiration of lymph node and by splenic imprint in a patient with acute promyelocytic leukemia. A tumor-necrosis factor-alpha (TNF-alpha) antagonist, the WP9QY peptide, was designed based on the crystal structure of the TNF-beta/TNF-receptor complex in order to overcome the disadvantages of macromolecules such as antibodies or soluble receptors by reducing the molecular size of TNF-alpha antagonists. Auxin promotes degradation of Aux/IAA proteins that prevent transcription factors of the auxin response factor (ARF) family from regulating auxin-responsive target genes. Identification of the orifice(s) connected with the bronchial circulation is carried out by the backflow which takes place from the pulmonary circulation after organ reperfusion is resumed. These results show that an experience-dependent interaction between visual and somatosensory inputs occurs during development, and that early exposure to abnormal visual-somatosensory experience modifies the organization of multisensory neurons in the superior colliculus.

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Deglycosylation of glucoamylase from Aspergillus niger: effects on structure, activity and stability. Before ischemia, glycolysis was accelerated in hypertrophied hearts, but to a greater extent in males, and did not differ between male bactrim drug allergy and female non-hypertrophied hearts. The results of this study show that recombinant interleukin-8 (IL-8) enhances the intracellular killing of Mycobacterium fortuitum by human granulocytes. The theoretical basis of stereoselectivity in drug targeting in terms of eudismic ratio and quantitative structure-activity relationship has been presented. Electron microscopy showed that, in these animals, erythrocytes infected with P.

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