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Axepta (Atomoxetine)

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Axepta is used as part of a total treatment program to increase the ability to pay attention and decrease impulsiveness and hyperactivity in children and adults with ADHD. Axepta comes as a capsule to take by mouth.

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

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Also known as: Atomoxetine


Axepta is an FDA-approved medication taken for the treatment of attention deficit hyperactivity disorder (ADHD). Its active ingredient, Atomoxetine, is a selective norepinephrine reuptake inhibitor. Atomoxetine increases the balance of certain chemicals in the brain (e.g., norepinephrine), thereby decreasing impulsive behavior and hyperactivity. Axepta may affect the attention span and behavior of the person taking it. It is also known as Atomoxetine, Attentrol, Tomoxetin, Attentin, Axepta.


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 Axepta 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 Axepta 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 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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