Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Fluvoxamine maleate
Drug ID BADD_D00951
Description Fluvoxamine is an antidepressant which functions pharmacologically as a selective serotonin reuptake inhibitor. Though it is in the same class as other SSRI drugs, it is most often used to treat obsessive-compulsive disorder. Fluvoxamine has been in use in clinical practice since 1983 and has a clinical trial database comprised of approximately 35,000 patients. It was launched in the US in December 1994 and in Japan in June 1999. As of the end of 1995, more than 10 million patients worldwide have been treated with fluvoxamine.
Indications and Usage Indicated predominantly for the management of depression and for Obsessive Compulsive Disorder (OCD) [FDA Label]. Has also been used in the management of bulimia nervosa [A250].
Marketing Status Prescription; Discontinued
ATC Code N06AB08
DrugBank ID DB00176
KEGG ID D00824
MeSH ID D016666
PubChem ID 5384136
TTD Drug ID D0M5JI
NDC Product Code 62559-160; 0832-1670; 62756-113; 71335-1974; 53296-0043; 60505-0164; 62559-159; 70518-1057; 60505-0166; 70518-3153; 72789-221; 70518-1789; 0228-2849; 0832-1672; 63629-8018; 59349-0009; 68788-7219; 68071-2337; 11722-063; 71335-2008; 70966-0026; 70518-1643; 76072-1003; 10370-176; 62559-158; 0832-1671; 71335-0264; 69452-183; 60505-0165; 0228-2848; 69452-182; 10370-175
Synonyms Fluvoxamine | Fluvoxadura | Fluvoxamin AL | Fluvoxamin beta | Fluvoxamin Stada | Fluvoxamin-neuraxpharm | Fluvoxamin neuraxpharm | Fluvoxamin-ratiopharm | Fluvoxamin ratiopharm | ratio-Fluvoxamine | ratio Fluvoxamine | Fluvoxamina Geminis | Geminis, Fluvoxamina | Fluvoxamine Maleate | Fluvoxamine Maleate, (E)-Isomer | Fluvoxamine, (Z)-Isomer | Luvox | Floxyfral | Fevarin | Dumirox | Faverin | Novo-Fluvoxamine | Novo Fluvoxamine | Nu-Fluvoxamine | Nu Fluvoxamine | PMS-Fluvoxamine | PMS Fluvoxamine | Desiflu | DU-23000 | DU 23000 | DU23000
Chemical Information
Molecular Formula C19H25F3N2O6
CAS Registry Number 61718-82-9
SMILES COCCCCC(=NOCCN)C1=CC=C(C=C1)C(F)(F)F.C(=CC(=O)O)C(=O)O
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Poisoning and toxicityCytochrome P450 2D6P10635T57392Not Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Gingivitis11.01.04.013; 07.09.03.003--
Glossitis07.14.01.001--Not Available
Goitre14.11.01.008; 05.02.01.001--Not Available
Haematemesis24.07.02.011; 07.12.02.002--Not Available
Haematospermia24.07.03.008; 21.03.03.003--Not Available
Haematuria20.02.01.006; 24.07.01.047--
Haemoptysis24.07.01.006; 22.02.03.004; 02.01.02.006--Not Available
Haemorrhoids24.10.02.002; 07.15.03.001--
Hallucination19.10.02.002--
Headache17.14.01.001--
Heart rate irregular13.14.04.003--Not Available
Hemiplegia17.01.04.002--Not Available
Henoch-Schonlein purpura24.07.06.003; 23.06.01.002; 10.02.02.004; 01.01.04.001--Not Available
Hepatitis09.01.07.004--Not Available
Hiccups07.01.06.009; 22.02.04.002--
Hostility19.05.01.003--Not Available
Hypercholesterolaemia14.08.01.001--Not Available
Hyperglycaemia14.06.02.002; 05.06.02.002--
Hyperhidrosis23.02.03.004; 08.01.03.028--
Hyperkinesia17.01.02.008--Not Available
Hypersensitivity10.01.03.003--
Hypersomnia19.02.05.001; 17.15.01.001--
Hypertension24.08.02.001--
Hypertonia17.05.02.001; 15.05.04.007--Not Available
Hyperventilation22.02.01.006; 19.01.02.004--Not Available
Hypoglycaemia05.06.03.001; 14.06.03.001--
Hypokalaemia14.05.03.002--
Hypokinesia17.01.02.009--Not Available
Hyporeflexia17.02.01.003--
Hypotension24.06.03.002--
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