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Use in Patients with Concomitant Illness Clinical experience with Fluoxetine in patients fluoxetine with concomitant systemic illness is limited. Sacramento, CA 95827, USA Toll Free Number: Revised: November 2017 principal display panel - 60 mg Tablet Bottle Label nivagen pharmaceuticals NDC Fluoxetine Tablets, USP 60 mg 30 Tablets pharmacist: Dispense the accompanying Medication Guide to real each patient Rx only Fluoxetine Fluoxetine. In one of these real studies, no dose-response relationship for effectiveness was demonstrated. This condition can be life-threatening and fluoxetine may include: agitation, hallucinations, coma or other changes in mental status coordination problems or muscle twitching (overactive reflexes) racing heartbeat, high or low blood real pressure sweating or fever nausea, vomiting, or diarrhea muscle rigidity dizziness flushing tremor seizures. Fluoxetine can cause sleepiness or may affect your ability to make decisions, think clearly, or react quickly. Patient Counseling Information See FDA-approved patient labeling (Medication Guide). Thase, ME; Corya, SA; Osuntokun, O; Case, M; Henley, DB; Sanger, TM; online Watson, SB; Dub, S (2007-02). This listing is not intended to include reactions real (1) already listed in previous tables or elsewhere in labeling, (2) for which a drug cause was remote, (3) which were so general as to be uninformative, (4) which were not considered. The size of the effect was related to baseline frequency, with greater reductions seen in patients with higher fluoxetine baseline frequencies. The most common adverse reaction (incidence at least 1 for Fluoxetine and greater than fluoxetine placebo) fluoxetine associated with discontinuation in 3 pediatric placebo-controlled trials (N 418 randomized; 228 Fluoxetine-treated; 190 placebo-treated) was mania/hypomania (1.8 for Fluoxetine-treated, 0 for placebo-treated). Take a Monoamine Oxidase Inhibitor fluoxetine (maoi). No unusual age-associated pattern of adverse reactions was observed in those elderly patients. Ask your healthcare provider or pharmacist if you are not sure if you take an maoi, including the antibiotic linezolid. Orap fluoxetine is a registered trademark of Teva Pharmaceuticals USA. Limited evidence is available concerning the longer-term effects of Fluoxetine on the development and maturation of children and adolescent patients. Starting Fluoxetine in a patient who is being treated with maois such as linezolid or intravenous methylene blue is also contraindicated because of an increased risk of serotonin syndrome see Dosage and Administration (2.7) and Warnings and Precautions (5.2). La fluoxtine peut avoir une interaction avec les mdicaments suivants: lalprazolam; la real clozapine; le flcanide; lhalopridol; les mdicaments contre les accs tels que la phnytone ou la carbamazpine; le tryptophane; la vinblastine; des anti-coagulants tels que la warfarine; lalmotriptan, le frovatriptan. Digestive System- Infrequent: dysphagia, gastritis, gastroenteritis, melena, stomach ulcer; Rare: bloody diarrhea, duodenal ulcer, esophageal ulcer, gastrointestinal hemorrhage, hematemesis, hepatitis, peptic real ulcer, stomach ulcer hemorrhage. Most Common Adverse Reactions Associated with Discontinuation in Major Depressive Disorder, Obsessive Compulsive Disorder, Bulimia, and Panic Disorder Placebo-Controlled Clinical Trials MDD, OCD, Bulimia, and Panic Disorder Combined (N 1533) fluoxetine MDD (N 392) OCD (N 266) Bulimia (N 450).

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