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Strattera (Atomoxetine)
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Strattera

Strattera modulates the activity of certain chemical messengers in the brain, which increases attention and decreases restlessness. It is a non-stimulant medicine. It is the most effective medicine for treating ADHD. It improves your behavior and enhances the quality of life.

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

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Also known as: Atomoxetine

Description

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

{name} is used to treat attention deficit hyperactivity disorder (ADHD).

Dosage

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

Overdose

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

Storage

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.

Contraindications

Do not use Strattera if you have used an MAO inhibitor in the past 14 days. A dangerous drug interaction could occur. MAO inhibitors include isocarboxazid, linezolid, methylene blue injection, phenelzine, rasagiline, selegiline, tranylcypromine, and others.

You should not use this medicine if you are allergic to atomoxetine, or if you have:

severe heart or blood vessel problems; narrow-angle glaucoma; or pheochromocytoma (tumor of the adrenal gland).

Strattera has caused stroke, heart attack, and sudden death in certain people. Tell your doctor if you have:

heart problems or a congenital heart defect; high blood pressure; or a family history of heart disease or sudden death.

To make sure this medicine is safe for you, tell your doctor if you or anyone in your family has ever had:

depression, mental illness, bipolar disorder, psychosis; suicidal thoughts or actions; low blood pressure; or liver disease.

Some young people have thoughts about suicide when first taking Strattera, or whenever the dose is changed. Your doctor will need to check your progress at regular visits. Your family or other caregivers should also be alert to changes in your mood or symptoms.

It is not known whether this medicine will harm an unborn baby. 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. Ask your doctor about any risk,

Strattera is not FDA-approved for use by anyone younger than 6 years old.

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Blocking nociceptive afferents by retrobulbar bupivacaine does not decrease nausea and vomiting after propofol-remifentanil anaesthesia. Subjects were assigned to either the ozone group, in which ozonated oil was applied to the surgical wound, or the control group cardura 4 mg dosage , in which non-ozonated oil was used as a control. Factors related to patient satisfaction with complete denture therapy. Multiple Sclerosis (MS) is a disabling chronic disease of the nervous system in which the myelin system of the central nervous system is deteriorated. Numerous studies have sought to assess the effectiveness of control measures aimed at reducing the spread of pathogens such as Methicillin-resistant Staphylococcus aureus (MRSA) in hospital settings. Patients on first ever OC orders in Northern Norway used inpatient services more after OC orders than before.

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Pretreatment AGR is a significant and independent predictive factor of prognosis. In contrast, verbal generative fluency decreased independent of lesion laterality, suggesting diffuse acute lesion effects on certain tasks mediated primarily by the left hemisphere. Transoesophageal echocardiographic images of the ascending, arch and descending aorta were evaluated in 128 patients to determine the aortic atheroma burden. Furthmore, CL 218,872 was relatively free of the ataxic and depressant side effects commonly associated with the benzodiazepines. Significance of the autonomic nervous system for vascular and volume regulation. The released factors then stimulate tumor cell signaling, which causes breast cancer cells to make increased amounts of osteolytic factors, such as parathyroid hormone-related protein (PTHrP), interleukin-11 (IL-11), and vascular endothelial growth factor (VEGF). The t 1/2 values for the acylated enzyme samples (lower pI) were reduced, succinylated asparaginase sharply and the acetylated enzyme less so. This genetic approach created mice with a KD of GR primarily confined to hypothalamic cell groups, including the PVN, sparing GR expression in other HPA axis limbic regulatory regions, and the pituitary. Of the 5 cases, 2 presented thalamic lacunar infarcts, 2 basal ganglia hemorrhages, and 1 dorsal midbrain hemorrhage on computed tomography scan. A comparative effectiveness study was done to compare 2 viscoelastic foam support surfaces.

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