Generic Strattera

1. Denomination

Strattera

2. Active Substance

Atomoxetine

3. Indications for Use.

— attention deficit/hyperactivity disorder in children of 6 years of age and more, adolescences and adults.

4. Action

Atomoxetine have an effect on all the disease symptoms, which may develop either at school and at home; the drug leads to long-lasting and stable improvement of the state.

5. Posology and Administration

The treatment should be done under survey of the doctor, experienced in the work with attention deficit/hyperactivity disorder patients.
Atomoxetine should be taken orally regardless of meal either during meal or as a single-shout daily dose in the morning. In the drug administration once daily adverse events appear, the patients may be recommended to take Atomoxetine 2 times/daily, dividing a dose in a morning intake and a late day/early evening one.
The drug withdrawal does not require a gradual decrease of a dose.

6. Counterindications

Hypersensitivity, closed-angle glaucoma, lactation period, childhood (less than 6 years of age).

7. Should Be Taken with Precautions, if…

Care should be taken in Atomoxetine application in patients with hypertension, tachycardia, cardiovascular diseases or brain circulation disorder, likewise in the states that may result in arterial hypotension.
Atomoxetine capsules are not intended for opening. Atomoxetine provokes eyes irritation. In the event of penetration of a capsule’s contents into eyes, rinse them with water immediately and seek a doctor’s attendance. Also the hands and contact surfaces should be rinsed with water.

8. Interface with Other Medications

Because of a possible interaction of Atomoxetine, this drug should be applied with care in combination with other medications and, as a rule, a doctor’s advice is needed.

9. Overdosing

Symptoms: drowsiness, agitation, hyperactivity, behavior disorder and gastric-intestinal tract disorders, pupil’s dilatation, tachycardia, dry mouth, convulsions, lethal outcome.

10. Side Effects

Dizziness, drowsiness, early morning awakening, insomnia, irritation, emotional instability; pupil’s dilatation; heartbeat, tachycardia; pain in the stomach, vomit, abdominal swelling, anorexia, reduction in the body mass; elevated perspiration, dermatitis, itch, rash, angioedema, hives; libido decrease, urinary difficulty, urine retention, ejaculation and erection disorders, anorgasmy, prostatitis; fatigability, flue.

11. Pregnancy and Lactation

Clinical practice of the use of Atomoxetine in pregnancy is insufficient, for this reason the drug should be administered in pregnancy only in the case if expected utility of the therapy for the mother far exceeds a potential risk for the fetus.
It is not known whether Atomoxetine excretes with human milk. If there is a need to administer the drug to a nursing mother caution is needed.

12. Driving

Atomoxetine administration may be accompanied with drowsiness. Owing to it the patients who take Atomoxetine should be careful while operating dangerous motor vehicles, including automobile, until they are confident that Atomoxetine does not provoke any disorders.

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