Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Isocarboxazid
Drug ID BADD_D01202
Description Isocarboxazid has the formula 1-benzyl-2-(5-methyl-3-isoxazolylcarbonyl)hydrazine-isocarboxazid. It is a monoamine oxidase inhibitor.[A31930] It is used in the treatment of major depression, dysthymic disorder, atypical disorder, panic disorder and the phobic disorders.[T115] It was first introduced by Roche pharmaceuticals, further developed by Validus pharms Inc and first FDA approved as a prescription drug on July 1st, 1959.
Indications and Usage Isocarboxazid is indicated for the treatment of the enduring and debilitating symptoms of depression that have not responded to other antidepressant drugs.[L1372] Depression is a common but serious mood disorder. The patient will present changes in its feelings, thoughts, and ability to handle everyday activities. For a mood disorder to be considered as depression, the symptoms should be present for at least two weeks.[L1375]
Marketing Status approved
ATC Code N06AF01
DrugBank ID DB01247
KEGG ID D02580
MeSH ID D007520
PubChem ID 3759
TTD Drug ID D0I2VK
NDC Product Code 55679-115; 30698-032
UNII 34237V843T
Synonyms Isocarboxazid
Chemical Information
Molecular Formula C12H13N3O2
CAS Registry Number 59-63-2
SMILES CC1=CC(=NO1)C(=O)NNCC2=CC=CC=C2
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Agitation19.06.02.001; 17.02.05.012--
Akathisia19.06.02.006; 17.01.02.002--
Amblyopia06.02.01.001--Not Available
Anxiety19.06.02.002--
Ataxia08.01.02.004; 17.02.02.001--
Chills15.05.03.016; 08.01.09.001--
Coma17.02.09.001--Not Available
Constipation07.02.02.001--
Diarrhoea07.02.01.001--
Discomfort08.01.08.003--Not Available
Dizziness02.11.04.006; 24.06.02.007; 17.02.05.003--
Dry mouth07.06.01.002--
Dysuria20.02.02.002--
Euphoric mood19.04.02.006--
Fluid retention20.01.02.003; 14.05.06.002--Not Available
Hallucination19.10.04.003--
Headache17.14.01.001--
Hyperhidrosis23.02.03.004; 08.01.03.028--
Hyperkinesia17.01.02.008--Not Available
Incontinence17.05.01.006; 07.01.06.011; 20.02.02.004--Not Available
Insomnia19.02.01.002; 17.15.03.002--
Lethargy19.04.04.004; 17.02.04.003; 08.01.01.008--
Loss of consciousness17.02.04.004--Not Available
Memory impairment17.03.02.003; 19.20.01.003--
Myoclonus17.02.05.008--Not Available
Nausea07.01.07.001--
Neuritis17.09.03.001--Not Available
Neuropathy peripheral17.09.03.003--Not Available
Orthostatic hypotension24.06.03.004; 17.05.01.020--Not Available
Palpitations02.11.04.012--
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ADReCS-Target
Drug Name ADR Term Target
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