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Axepta (Atomoxetine)
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Axepta

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

Description

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.

Dosage

Take Axepta orally with or without food. If stomach upset occurs, take with food to reduce stomach irritation. Take Axepta with a full glass of water. Do not chew, crush, open or take the capsules apart. Take Axepta at the same time each day. To achieve the most effective results, do not stop taking Axepta suddenly.

Overdose

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Overdose symptoms may include drowsiness, dizziness, stomach problems, tremors, or unusual behavior.

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 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.

Contraindications

Do not use Axepta 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).

Axepta 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 Axepta, 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 Axepta.

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 Axepta. Ask your doctor about any risk,

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

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Effectiveness of a patient education intervention in enhancing the self-efficacy of hospitalized patients to recognize and report acute deteriorating conditions. Duct tape for the treatment of common warts in adults: a double-blind randomized controlled trial. The Rayleigh hypothesis (RH) is often invoked in the theoretical and numerical treatment of rough surface scattering in order to decouple the analytical form of the scattered field. Although these diseases most commonly present in childhood, some rarely present in adulthood, and thus all endocrinologists must be familiar with these syndromes. In order to point out molecular markers expressed in this early neuroectodermic commitment, we used a cDNA subtractive hybridization method.

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