Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Maprotiline
Drug ID BADD_D01350
Description Maprotiline is a tetracyclic antidepressant with similar pharmacological properties to tricyclic antidepressants (TCAs). Similar to TCAs, maprotiline inhibits neuronal norepinephrine reuptake, possesses some anticholinergic activity, and does not affect monoamine oxidase activity. It differs from TCAs in that it does not appear to block serotonin reuptake. Maprotiline may be used to treat depressive affective disorders, including dysthymic disorder (depressive neurosis) and major depressive disorder. Maprotiline is effective at reducing symptoms of anxiety associated with depression.
Indications and Usage For treatment of depression, including the depressed phase of bipolar depression, psychotic depression, and involutional melancholia, and may also be helpful in treating certain patients suffering severe depressive neurosis.
Marketing Status approved; investigational
ATC Code N06AA21
DrugBank ID DB00934
KEGG ID D02566
MeSH ID D008376
PubChem ID 4011
TTD Drug ID D03KQF
NDC Product Code Not Available
UNII 2U1W68TROF
Synonyms Maprotiline | Maprotilin | N-Methyl-9,10-ethanoanthracene-9(10H)-propylamine | Dibencycladine | Psymion | Ludiomil | Maprolu | Maprotilin Holsten | maprotilin von ct | Maprotilin-neuraxpharm | Maprotilin neuraxpharm | Maprotilin-ratiopharm | Maprotilin ratiopharm | Maprotilin-TEVA | Maprotilin TEVA | Maprotiline Hydrochloride | Hydrochloride, Maprotiline | Maprotiline Mesylate | Mesylate, Maprotiline | Mirpan | Novo-Maprotiline | Novo Maprotiline | Ba-34,276 | Ba34,276 | Deprilept
Chemical Information
Molecular Formula C20H23N
CAS Registry Number 10262-69-8
SMILES CNCCCC12CCC(C3=CC=CC=C31)C4=CC=CC=C24
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)
Dermatitis atopic23.03.04.016; 10.01.04.004--Not Available
Diarrhoea07.02.01.001--
Disorientation19.13.01.002; 17.02.05.015--Not Available
Dizziness17.02.05.003; 02.11.04.006; 24.06.02.007--
Drug withdrawal syndrome19.07.06.013; 08.06.02.004--Not Available
Dry mouth07.06.01.002--
Dysarthria19.19.03.001; 17.02.08.001--
Dysgeusia17.02.07.003; 07.14.03.001--
Dyskinesia17.01.02.006--
Dyspepsia07.01.02.001--
Dysphagia07.01.06.003--
Ear disorder04.03.01.001--Not Available
Electrocardiogram QRS complex13.14.05.034--Not Available
Electroencephalogram abnormal13.07.03.001--Not Available
Endocrine disorder05.09.01.001--Not Available
Eosinophilia01.02.04.001--
Erythema multiforme23.03.01.003; 10.01.03.015--
Extrapyramidal disorder17.01.02.007--
Eye disorder06.08.03.001--Not Available
Face oedema23.04.01.004; 10.01.05.002; 08.01.07.003--
Fatigue08.01.01.002--
Feeling abnormal08.01.09.014--Not Available
Flushing08.01.03.025; 24.03.01.002; 23.06.05.003--
Gait disturbance17.02.05.016; 08.01.02.002; 15.03.05.013--
Galactorrhoea21.05.02.002; 05.03.04.002--Not Available
Gastrointestinal disorder07.11.01.001--Not Available
Gastrointestinal pain07.01.05.005--
Generalised tonic-clonic seizure17.12.01.002--Not Available
Gynaecomastia21.05.04.003; 05.05.02.003--
Hallucination19.10.04.003--
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ADReCS-Target
Drug Name ADR Term Target
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