Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Maprotiline hydrochloride
Drug ID BADD_D01351
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 Prescription; Discontinued
ATC Code N06AA21
DrugBank ID DB00934
KEGG ID D00818
MeSH ID D008376
PubChem ID 71478
TTD Drug ID D03KQF
NDC Product Code 17337-0527
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 C20H24ClN
CAS Registry Number 10347-81-6
SMILES CNCCCC12CCC(C3=CC=CC=C31)C4=CC=CC=C24.Cl
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)
Abdominal pain07.01.05.002--
Accommodation disorder06.02.04.001--Not Available
Agitation17.02.05.012; 19.06.02.001--
Akathisia19.06.02.006; 17.01.02.002--
Alopecia23.02.02.001--
Anxiety19.06.02.002--
Arrhythmia02.03.02.001--Not Available
Asthenia08.01.01.001--Not Available
Ataxia08.01.02.004; 17.02.02.001--
Atrioventricular block02.03.01.002--Not Available
Blood glucose decreased13.02.02.001--Not Available
Blood glucose increased13.02.02.002--Not Available
Confusional state19.13.01.001; 17.02.03.005--
Constipation07.02.02.001--
Delusion19.10.01.001--
Derealisation19.10.02.001--Not Available
Diarrhoea07.02.01.001--
Disorientation19.13.01.002; 17.02.05.015--Not Available
Dizziness24.06.02.007; 17.02.05.003; 02.01.02.004--
Dry mouth07.06.01.002--
Dysarthria19.19.03.001; 17.02.08.001--
Dysgeusia17.02.07.003; 07.14.03.001--
Dyspepsia07.01.02.001--
Dysphagia07.01.06.003--
Electroencephalogram abnormal13.07.03.001--Not Available
Extrapyramidal disorder17.01.02.007--
Fatigue08.01.01.002--
Flushing24.03.01.002; 23.06.05.003; 08.01.03.025--
Hallucination19.10.02.002--
Headache17.14.01.001--
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