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Label for FLUVOXAMINE MALEATE

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Label for FLUVOXAMINE MALEATE Highlights Of Prescribing Information Ramelteon: Should not be used in combination with fluvoxamine (5.8). These highlights do not include all the information needed to use Theophylline: Clearance decreased; reduce theophylline dose by one-third FLUVOXAMINE MALEATE TABLETS safely and effectively. See full (5.8). Warfarin: Plasma concentrations increased and prothrombin times prescribing information for FLUVOXAMINE MALEATE TABLETS. prolonged; monitor prothrombin time and adjust warfarin dose accordingly (5.8). Other Drugs Affecting Hemostasis: Increased risk of bleeding with FLUVOXAMINE MALEATE Tablets for oral administration concomitant use of NSAIDs, aspirin, or other drugs affecting coagulation Initial U.S. Approval: 1994 (5.8, 5.10). See Contraindications (4). Warning: Suicidality and Antidepressants • Discontinuation: Symptoms associated with discontinuation have been See full prescribing information for complete boxed warning. reported (5.9). Abrupt discontinuation not recommended. See Dosage And Increased risk of suicidal thinking and behavior in children, adolescents, Administration (2.8). and young adults taking antidepressants for major depressive disorder and • Activation of mania/hypomania has occurred (5.11). other psychiatric disorders. Fluvoxamine Maleate Tablets are not approved • for use in pediatric patients except those with obsessive compulsive Seizures: Avoid administering fluvoxamine in patients with unstable epilepsy; monitor patients with controlled epilepsy; discontinue treatment if disorder (5.1). seizures occur or frequency increases (5.12). ----------------------------------Recent Major Changes-------------------------------­ • Hyponatremia: May occur with SSRIs and SNRIs, including Fluvoxamine Warnings and Precautions, Serotonin Syndrome (5.2) 1/2017 Maleate Tablets. The elderly may be at increased risk. Consider discontinuing in patients with symptomatic hyponatremia (5.13). ----------------------------------Indications And Usage--------------------------------- • Concomitant illness: Use caution in patients with diseases or conditions that Fluvoxamine Maleate Tablets are indicated for the treatment of obsessions and affect hemodynamic responses or metabolism (5.14). Patients with impaired compulsions in patients with obsessive compulsive disorder (OCD) (1). liver function may require a lower starting dose and slower titration (2.3). -------------------------------Dosage And Administration----------------------------­ ------------------------------Adverse Reactions ----------------------------------------­ • Adults: Recommended starting dose is 50 mg at bedtime, with increases of • Most common reactions in controlled trials with adult OCD and 50 mg every 4 to 7 days as tolerated to maximum effect, not to exceed depression patients (incidence ≥5% and at least twice that for placebo) 300 mg/day. Daily doses over 100 mg should be divided (2.1). were nausea, somnolence, insomnia, asthenia, nervousness, dyspepsia, • Children and adolescents (8-17 years): Recommended starting dose is 25 mg at abnormal ejaculation, sweating, anorexia, tremor, and vomiting (6.2). bedtime, with increases of 25 mg every 4 to 7 days as tolerated to maximum Using the above rule, the following events were also identified: effect, not to exceed 200 mg/day (8-11 years) or 300 mg/day (12-17 years). anorgasmia, decreased libido, dry mouth, rhinitis, taste perversion, and Daily doses over 50 mg should be divided (2.2). urinary frequency in patients with OCD; and agitation, depression, • Hepatically impaired: Decreased clearance may require modified dose and dysmenorrhea, flatulence, hyperkinesia, and rash in pediatric patients titration (2.3). with OCD. • Extended treatment: Adjust dose to maintain lowest effective dose; reassess To report Suspected Adverse Reactions, call toll free at 1-800-308-6755 patients periodically (2.7). (phone); 1-651-641-0341 (fax); or FDA at 1-800-FDA-1088 or • Discontinuation: Gradual dose reduction is recommended (2.8, see www.fda.gov/Medwatch. Warnings And Precautions [5.9]). -------------------------------Drug Interactions ----------------------------------------­ -------------------------------Dosage Forms And Strengths -----------------------------­ Drug Interactions (not described in Contraindications or Warnings And • 25 mg Tablets, 50 mg Tablets, and 100 mg Tablets (3) Precautions) include the following: Drugs Inhibiting or Metabolized by Cytochrome P450: Fluvoxamine inhibits ------------------------------------Contraindications---------------------------------------­ several cytochrome P450 isoenzymes (CYP1A2, CYP2C9, CYP3A4, and • Coadministration of tizanidine, thioridazine, alosetron, pimozide (4.1) CYP2C19). Carbamazepine: Elevated carbamazepine levels and symptoms of • Serotonin Syndrome and MAOIs: Do not use MAOIs intended to treat toxicity with coadministration (7.2). Sumatriptan: Rare postmarketing reports psychiatric disorders with Fluvoxamine Maleate Tablets or within 14 days of of weakness, hyperreflexia, and incoordination following use of an SSRI and stopping treatment with Fluvoxamine Maleate Tablets. Do not use sumatriptan. Monitor appropriately if concomitant treatment is clinically Fluvoxamine Maleate Tablets within 14 days of stopping an MAOI intended warranted (7.2). Tacrine: Coadministration increased tacrine Cmax and AUC to treat psychiatric disorders. In addition, do not start Fluvoxamine Maleate five- and eight-fold and caused nausea, vomiting, sweating, and diarrhea (7.2). Tablets in a patient who is being treated with linezolid or intravenous Tricyclic Antidepressants (TCAs): Coadministration significantly increased methylene blue (4.2) plasma TCA levels. Use caution; monitor plasma TCA levels; reduce TCA dose if indicated (7.2). Tryptophan: Severe vomiting with coadministration (7.2). --------------------------------Warnings And Precautions -------------------------------­ Diltiazem: Bradycardia with coadministration (7.3). Propranolol or • Suicidality: Monitor for clinical worsening and suicide risk (5.1). metoprolol: Reduce dose if coadministered and titrate more cautiously (7.3). • Bipolar disorder: Screen for bipolar disorder (5.1). -------------------------Use In Specific Populations ----------------------------------­ Specific populations not discussed in Dosage and Administration or • Serotonin Syndrome: Serotonin syndrome has been reported with SSRIs and Warnings and Precautions include: SNRIs, including Fluvoxamine Maleate Tablets, both when taken alone, but especially when co-administered with other serotonergic agents (including • Pregnancy: Consider both potential risks and benefits when treating a triptans, tricyclic antidepressants, fentanyl, lithium, tramadol, tryptophan, pregnant woman. Infants exposed to SSRIs late in pregnancy have buspirone, amphetamines, and St. John's Wort). If such symptoms occur, developed various complications and may be at risk for persistent discontinue Fluvoxamine Maleate Tablets and initiate supportive treatment. pulmonary hypertension of the newborn (PPHN) (2.4, 8.1). If concomitant use of Fluvoxamine Maleate Tablets with other serotonergic • Nursing mothers: Fluvoxamine is secreted in human breast milk (8.3). drugs is clinically warranted, patients should be made aware of a potential • Pediatric: Monitor weight and growth; effects of long-term use on growth, increased risk for serotonin syndrome, particularly during treatment initiation congnitive behavioral development, and maturation have not been studied and dose increases. (5.2). (8.4). • Angle Closure Glaucoma: Angle closure glaucoma has occurred in patients with • Geriatric: Use of a lower starting dose may be warranted. Titrate slowly untreated anatomically narrow angles treated with antidepressants (5.3). during initiation of therapy (2.3, 8.5). • Other potentially important drug interactions. Benzodiazepines: Use with • Smokers: Smokers had a 25% increase in fluvoxamine metabolism (7.4). caution. Coadministration with diazepam is generally not advisable (5.8). Clozapine: Clozapine levels may be increased and produce orthostatic See 17 For Patient Counseling Information and the FDA-Approved hypotension or seizures (5.8). Methadone: Coadministration may produce Medication Guide opioid intoxication. Discontinuation of fluvoxamine may produce opioid Rev 1/2017 withdrawal (5.8). Mexiletine: Monitor serum mexiletine levels (5.8). 1 Reference ID: 4036397 FULL PRESCRIBING INFORMATION: CONTENTS* 7 DRUG INTERACTIONS SUICIDALITY AND ANTIDEPRESSANT DRUGS 7.1 Potential Interactions with Drugs that Inhibit or are Metabolized by 1 INDICATIONS AND USAGE Cytochrome P450 Isoenzymes 1.1 Obssesive-Compulsive Disorder 7.2 CNS Active Drugs 2 DOSAGE AND ADMINISTRATION 7.3 Other Drugs 2.1 Adults 7.4 Effects of Smoking on Fluvoxamine Metabolism 2.2 Pediatric Population (children and adolescents) 7.5 Electroconvulsive Therapy (ECT) 2.3 Elderly or Hepatically Impaired Patients 8 USE IN SPECIFIC POPULATIONS 2.4 Pregnant Women During the Third Trimester 8.1 Pregnancy 2.5 Switching a Patient To or From a Monoamine Oxidase Inhibitor 8.2 Labor And Delivery (MAOI) Intended to Treat Psychiatric Disorders 8.3 Nursing Mothers 2.6 Use of Fluvoxamine Maleate Tablets with Other MAOIs such as 8.4 Pediatric Use Linezolid or Methylene Blue 8.5 Geriatric Use 2.7 Maintenance/Continuation Extended Treatment 9 DRUG ABUSE AND DEPENDENCE 2.8 Discontinuation of Treatment with Fluvoxamine Maleate Tablets 9.1 Controlled Substance 3 DOSAGE FORMS AND STRENGTHS 9.2 Physical and Psychological Dependence 4 CONTRAINDICATIONS
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