- Appetite loss;
- Stomach;
- Dyspepsia (digestion upset);
- Nausea;
- Drowsiness;
- Early morning awakenings.
Increased side-effects may lead to cancellation of the treatment.
Do Not Use Strattera If you:
- are pregnant, planning to become pregnant, or breastfeeding.
- have liver problems.
- have an eye problem called narrow angle glaucoma.
- have or had suicide thoughts or actions.
- have mental problems, psychosis, mania, bipolar illness, or depression.
- have heart problems, heart defects, irregular heart beat, high blood pressure, or low blood pressure.
- do not combine Strattera with a monoamine oxidase inhibitor.
Serious Reactions to Strattera:
- trouble sleeping
- aggressiveness
- anxiety
- depression
- agitation
- impulsivity
- panic attacks
- irritability
- hostility
- restlessness
- mania
- suicide thoughts
Strattera Side-effects are observed during the first month of ADHD treatment and are not harmful to the child’s health.
The Food and Drug Administration (U.S.) warning information on Strattera:
“…Pooled analyses of short-term (from 6 to 18 weeks) placebo-controlled trials of Srattera in children and adolescents (a total of 12 trials involving over 2200 patients, including 11 trials in ADHD and 1 trial in enuresis) have revealed a greater risk of suicidal ideation early during treatment in those receiving Strattera compared to placebo. The average risk of suicidal ideation in patients receiving Strattera was 0.4% (5/1357 patients), compared to none in placebo-treated patients (851 patients). Howewer, no suicides occurred in these trial…”.
Patients who are started on therapy should be monitored closely for suicidality (suicidal thinking and behavior), clinical worsening, or unusual changes in behavior.
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