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Or in a crisis, text NAMI to All FDA black box warnings are at the end of this fact sheet. Bupropion is an antidepressant medication that works in the brain. It is approved for the treatment of major depressive disorder MDD, seasonal affective disorder SAD, and to help people quit smoking smoking cessation.

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This means you do not have to taper off the use of Strattera if you decide to stop taking the medication. However, the tradeoff is that it may take a month or two for the medication to reach its full efficacy. Take our 2-minute Attention Deficit Hyperactivity Disorder quiz to see if you may benefit from further diagnosis and treatment.

They should take the medication in the exact amount prescribed by their doctor. Are there potential interaction issues for people taking Strattera and any other drugs? Do not take Strattera if you, or your child, have taken an MAO inhibitor in the past two weeks, as a dangerous interaction effect could occur. There are also many drugs which are known to interact with Strattera in major, moderate, or mild ways, so let your doctor know what other medications you are taking before you begin Strattera therapy.

Are there any other medical conditions that would make someone ineligible for Strattera therapy? You should not take Strattera if you are allergic to anything in the medication. Also talk to your doctor if you have had heart problems, high or low blood pressure, liver problems, or a history of mental illness such as depression or bipolar disorder. Also, if you or your child has a history of suicidal thoughts or action, talk to your doctor about the risks.

Dosage for children varies depending on the age and weight of a child. Strattera can be taken with or without food. So at administration of drug it is possible to take alcohol and greasy food that is not recommended at taking of any other type of viagra. The effect of Viagra Soft Flavored comes in 30 minutes after reception, and lasts for 4 hours. Brand Cialis improves erection and helps to achieve a successful sexual intercourse.

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In the clinical trials for atomoxetine in children and adolescents, the most common adverse events were upset stomach, decreased appetite, nausea or vomiting, dizziness, tiredness, and mood swings. This medication has a boxed warning for the increased risk of suicidal ideation in children and adolescents. Patients taking this medication should be monitored appropriately and observed closely for clinical worsening, suicidality, and unusual changes in behavior, especially during the initial few months of a course of drug therapy, or at times of dose changes. Other important warnings include the risk of severe liver damage and potential for serious cardiovascular events. Conferences Conference Coverage. Publications All Publications.

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