Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Vortioxetine hydrobromide
Drug ID BADD_D02372
Description Vortioxetine is an atypical antipsychotic and antidepressant indicated for the treatment of major depressive disorder (MDD). It is classified as a serotonin modulator and simulator (SMS) as it has a multimodal mechanism of action towards the serotonin neurotransmitter system whereby it simultaneously modulates one or more serotonin receptors and inhibits the reuptake of serotonin. More specifically, vortioxetine acts via the following biological mechanisms: as a serotonin reuptake inhibitor (SRI) through inhibition of the serotonin transporter, as a partial agonist of the 5-HT1B receptor, an agonist of 5-HT1A, and an antagonist of the 5-HT3, 5-HT1D, and 5-HT7 receptors. SMSs were developed because there are many different subtypes of serotonin receptors, however, not all of these receptors appear to be involved in the antidepressant effects of SRIs. Some serotonin receptors seem to play a relatively neutral or insignificant role in the regulation of mood, but others, such as 5-HT1A autoreceptors and 5-HT7 receptors, appear to play an oppositional role in the efficacy of SRIs in treating depression.
Indications and Usage Vortioxetine is indicated for the treatment of major depressive disorder (MDD).
Marketing Status Prescription; Discontinued
ATC Code N06AX26
DrugBank ID DB09068
KEGG ID D10185
MeSH ID D000078784
PubChem ID 56843850
TTD Drug ID D03WEX
NDC Product Code 68554-0110; 53747-072; 50370-0051; 42973-236; 50370-0054; 45562-1135
Synonyms Vortioxetine | 1-(2-(2,4-Dimethylphenylsulfanyl)phenyl)piperazine | Lu AA21004 | LuAA21004 | Lu-AA21004 | Brintellix | Vortioxetine Hydrobromide
Chemical Information
Molecular Formula C18H23BrN2S
CAS Registry Number 960203-27-4
SMILES CC1=CC(=C(C=C1)SC2=CC=CC=C2N3CCNCC3)C.Br
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Abnormal dreams19.02.03.001; 17.15.02.001--Not Available
Anger19.04.02.001--Not Available
Constipation07.02.02.001--
Diarrhoea07.02.01.001--
Dizziness17.02.05.003; 02.01.02.004; 24.06.02.007--
Dry mouth07.06.01.002--
Dysgeusia17.02.07.003; 07.14.03.001--
Dyspepsia07.01.02.001--
Flatulence07.01.04.002--
Flushing23.06.05.003; 08.01.03.025; 24.03.01.002--
Headache17.14.01.001--
Hypersensitivity10.01.03.003--
Hypomania19.16.02.001--Not Available
Hyponatraemia14.05.04.002--
Mania19.16.02.002--
Mood swings19.04.03.001--Not Available
Nausea07.01.07.001--
Pruritus23.03.12.001--
Rhinorrhoea22.02.05.010--
Serotonin syndrome17.05.02.004; 15.05.04.016; 12.03.01.041--Not Available
Suicide attempt19.12.01.004--
Vertigo04.04.01.003; 17.02.12.002--
Vomiting07.01.07.003--
Muscle tightness15.05.03.007--Not Available
Female sexual dysfunction21.03.02.004; 19.08.05.001--Not Available
Male sexual dysfunction21.03.02.012; 19.08.05.003--Not Available
Abdominal wall haemorrhage24.07.02.036; 07.16.05.002--Not Available
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