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Strattera (Atomoxetine)
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Strattera

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

Description

Strattera 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. Strattera may affect the attention span and behavior of the person taking it. It is also known as Atomoxetine, Attentrol, Tomoxetin, Attentin, Axepta.

Dosage

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