Fluvoxamine
Floxyfral · ATC code N06AB08
Also known as: Fluvoxamin, Fluvoksamin, fluvoxamine maleate · Brand names: Floxyfral, Fevarin, Fluvoxamin Neuraxpharm, Faverin, Revoxin
- Key facts
- Active substance
- Fluvoxamine
- Drug class
- Selective serotonin reuptake inhibitor
- ATC code
- N06AB08
- Authorisation
- authorised nationally; no central EU authorisation
- Information as of
- 2026-10-27
Boxed warning
Antidepressants increased the risk compared to placebo of suicidal thinking and behavior (suicidality) in children, adolescents, and young adults in short-term studies of major depressive disorder (MDD) and other psychiatric disorders. Anyone considering the use of Fluvoxamine Maleate Tablets or any other antidepressant in a child, adolescent, or young adult must balance this risk with the clinical need. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24; there was a reduction in risk with antidepressants compared to placebo in adults aged 65 and older. Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide. Patients of all ages who are started on antidepressant therapy should be monitored appropriately and observed closely for clinical worsening, suicidality, or unusual changes in behavior. Families and caregivers should be advised of the need for close observation and communication with the prescriber. Fluvoxamine Maleate Tablets are not approved for use in pediatric patients except for patients with obsessive compulsive disorder (OCD) [see Warnings and Precautions (5.1)].
Key facts
Fluvoxamine is a selective serotonin reuptake inhibitor (SSRI). Per the US label it is used to treat obsessions and compulsions in obsessive compulsive disorder (OCD).
What it is used for
- Obsessive compulsive disorder (OCD) in adults and in children and adolescents (ages 8-17)
Dosing
- Adults: start 50 mg once daily at bedtime, increase by 50 mg every 4 to 7 days; not to exceed 300 mg per day
- Children and adolescents (8-17 years): start 25 mg at bedtime, increase by 25 mg every 4 to 7 days; up to age 11 not to exceed 200 mg/day
- Daily doses above 100 mg (children: above 50 mg) given in two divided doses, the larger at bedtime
- Elderly and hepatic impairment: the initial dose and titration may need modification
- At least 14 days between fluvoxamine and MAOIs
Contraindications
- Coadministration of tizanidine, thioridazine, alosetron or pimozide
- MAOIs for psychiatric disorders concomitantly or within 14 days
- Starting in patients treated with linezolid or intravenous methylene blue
Important warnings
- Boxed warning: antidepressants increase the risk of suicidal thinking and behavior in children, adolescents and young adults; monitor closely
- Serotonin syndrome, especially with other serotonergic drugs
- Increased bleeding risk, particularly with NSAIDs, aspirin or warfarin
- May trigger angle closure attacks in patients with anatomically narrow angles
- Discontinuation symptoms with abrupt stopping; reduce gradually
Side effects
- Most common: nausea, somnolence, insomnia, asthenia, nervousness, dyspepsia, abnormal ejaculation, sweating, anorexia, tremor, vomiting
- 22% discontinued due to adverse reactions in trials, most often nausea (9%)
Interactions
- Inhibits several CYP enzymes: tizanidine, thioridazine, alosetron and pimozide are contraindicated
- Theophylline clearance markedly decreased, reduce its dose; elevated levels also with clozapine and tricyclic antidepressants
- Warfarin, NSAIDs, aspirin: increased bleeding risk; diltiazem: bradycardia reported
- Smoking increases fluvoxamine metabolism
Pregnancy and breastfeeding
- SSRI exposure in the month before delivery has been associated with an increased risk of postpartum hemorrhage
- Fluvoxamine is present in human milk; diarrhea, vomiting, decreased sleep and agitation in infants have been reported
Summary of the official product information, written with AI (Claude, Anthropic) on 2026-10-28. Every number was checked automatically against the original text. Not reviewed by a physician – the full official text is authoritative.
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For patients
Patient information (US)
Authorisation and brand names by country
Medicines with exactly this active-substance composition, as listed in the national registers – alphabetical and without ranking. Whether a product is currently available is not shown here.
Austria
- FloxyfralViatris Healthcare Limited · 1 register entry
Source: EMA – Article 57 product data (EU/EEA), as of 2026-10-28
Germany
- FevarinViatris Healthcare Gmbh · 1 register entry
- Fluvoxamin NeuraxpharmNeuraxpharm Arzneimittel Gmbh · 1 register entry
Source: EMA – Article 57 product data (EU/EEA), as of 2026-10-28
Turkey
- FaverinABBOTT LABORATUARLARI İTHALAT İHRACAT VE TİC. LTD. ŞTİ. · 2 register entries
- RevoxinRECORDATİ İLAÇ SAN. VE TİC. A.Ş. · 2 register entries
Source: TİTCK – Ruhsatlı Beşeri Tıbbi Ürünler Listesi, as of 2026-10-16
Brand names in 24 more European countries
- Belgium
- Floxyfral, Fluvoxamine Eg
- Bulgaria
- Феварин
- Croatia
- Fevarin
- Cyprus
- Faverin
- Czechia
- Fevarin
- Estonia
- Fevarin
- Finland
- Fluvosol
- France
- Floxyfral, Fluvoxamine Arrow, Fluvoxamine Viatris
- Greece
- Dumyrox
- Hungary
- Fevarin
- Ireland
- Faverin
- Italy
- Dumirox, Fevarin, Fluvoxamina Eg, Maveral
- Latvia
- Fevarin
- Lithuania
- Fevarin
- Luxembourg
- Floxyfral, Fluvoxamine Eg
- Malta
- Dumyrox
- Netherlands
- Fevarin, Fluvoxaminemaleaat Aurobindo, Fluvoxaminemaleaat Genthon, Fluvoxaminemaleaat Mylan, Fluvoxaminemaleaat Sandoz
- Norway
- Fevarin
- Poland
- Fevarin
- Portugal
- Dumyrox, Fluvoxamina Generis
- Romania
- Fevarin
- Slovakia
- Fevarin
- Spain
- Dumirox, Fluvoxamina Sandoz
- Sweden
- Fevarin
EMA – Article 57 product data (EU/EEA), 2026-10-28
Medelix receives no money from pharmaceutical companies. Brand names are listed alphabetically and without ranking.
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Sources
- U.S. Food and Drug Administration. fluvoxamine maleate (ANI Pharmaceuticals, Inc.) – Prescribing Information, 2025-08-04. DailyMed (NLM), 2026-10-27. https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7ecd83ec-88f5-4f85-9cc2-9068375d8820
- EMA – Article 57 product data (EU/EEA), 2026-10-28. https://www.ema.europa.eu/en/human-regulatory-overview/post-authorisation/data-medicines-iso-idmp-standards-post-authorisation/public-data-article-57-database
- EMA – Article 57 product data (EU/EEA), 2026-10-28. https://www.ema.europa.eu/en/human-regulatory-overview/post-authorisation/data-medicines-iso-idmp-standards-post-authorisation/public-data-article-57-database
- TİTCK – Ruhsatlı Beşeri Tıbbi Ürünler Listesi, 2026-10-16. https://www.titck.gov.tr/dinamikmodul/85
- Wikidata (CC0): ATC N06AB.
Editorial: Medelix editorial team · last updated 2026-10-27 · How these pages are made · Report an error
Source: U.S. Food and Drug Administration (FDA), prescribing information, via DailyMed (NLM); public domain. Not advertising, not a treatment recommendation. For questions about your own treatment, ask your doctor or pharmacist.