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Strattera may be taken with or without food.If Strattera should not be taken during pregnancy unless its benefits justify the potential risk to the baby. It is not known whether Strattera makes its way into breast milk. Patients who were pubertal (girls greater than 8 to less than 13 years old, boys greater than 9 to less than 14 years old) or late pubertal (girls greater than 13 years old, boys greater than 14 years old) had average weight and height gains that were close to or exceeded those predicted after three years of treatment.
Strattera Missed DoseCall your child's health care professional right away if your child or teenager has new or increased thoughts of suicide or has changes in mood or behavior like becoming irritable or anxious. Regularly monitor your child for these behavioral changes.You may get drowsy or dizzy. Do not drive, use machinery, or do anything that needs mental alertness until you know how this medicine affects you. Do not stand or sit up quickly, especially if you are an older patient. This reduces the risk of dizzy or fainting spells. Alcohol can make you more drowsy and dizzy. Avoid alcoholic drinks.Do The daily dose of Strattera can be taken as a single dose in the morning, or divided into two equal doses taken in the morning and late afternoon or early evening. Strattera PrecautionsThe complete text of the Medication Guide is reprinted at the end of this document. Patients should be advised of the following issues and asked to alert their prescriber if these occur while taking Strattera. Suicide Risk - Patients, their families, and their caregivers should be encouraged to be alert to the emergence of anxiety, agitation, panic attacks, insomnia, irritability, hostility, aggressiveness, impulsivity, akathisia (psychomotor restlessness), hypomania, mania, other unusual changes in behavior, depression, and suicidal ideation, especially early during Strattera treatment and when the dose is adjusted. Strattera NotesLaboratory and/or medical tests (e.g., pulse and blood pressure, liver function tests) should be performed periodically to monitor your progress or check for side effects. Remember that your doctor has prescribed this medication because he or she has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects. Tell your doctor immediately if any of these unlikely but serious side effects occur: weight loss decrease in sexual ability/desire (e.g., impotence, ejaculation problems) difficulty urinating unusually fast/irregular heartbeat fainting This medication may rarely cause serious problems such as heart attacks or stroke. Strattera WarningThe data in the following tables and text cannot be used to predict the incidence of side effects in the course of usual medical practice where patient characteristics and other factors differ from those that prevailed in the clinical trials. Similarly, the cited frequencies cannot be compared with data obtained from other clinical investigations involving different treatments, uses, or investigators. The cited data provide the prescribing physician with some basis for estimating the relative contribution of drug and non-drug factors to the adverse event incidence in the population studied. Child and Adolescent Clinical Trials Reasons for discontinuation of treatment due to adverse events in child and adolescent clinical trials - In acute child and adolescent placebo-controlled trials, 3.5% (15/427) of atomoxetine subjects and 1.4% (4/294) placebo subjects discontinued for adverse events. |
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