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)
Nervousness19.06.02.003--Not Available
Neuropathy peripheral17.09.03.003--Not Available
Nightmare19.02.03.003--Not Available
Oedema08.01.07.006; 14.05.06.010--Not Available
Oedema peripheral08.01.07.007; 02.05.04.007; 14.05.06.011--
Orthostatic hypotension24.06.03.004; 17.05.01.020--Not Available
Osteoarthritis15.01.04.001--Not Available
Palpitations02.11.04.012--
Pancytopenia01.03.03.003--Not Available
Paraesthesia23.03.03.094; 17.02.06.005--
Petechiae01.01.03.002; 24.07.06.004; 23.06.01.003--Not Available
Photosensitivity reaction23.03.09.003--
Pollakiuria20.02.02.007--
Pruritus23.03.12.001--
Purpura23.06.01.004; 01.01.04.003; 24.07.06.005--
Pyrexia08.05.02.003--
Rash23.03.13.001--Not Available
Rash erythematous23.03.13.029--Not Available
Rash maculo-papular23.03.13.004--
Salivary hypersecretion07.06.01.009--Not Available
Seizure17.12.03.001--
Sensory loss17.02.07.007--Not Available
Shock24.06.02.002--Not Available
Sinus tachycardia02.03.03.010--
Skin disorder23.03.03.007--Not Available
Sleep disorder19.02.04.001--Not Available
Somnolence19.02.05.003; 17.02.04.006--
Speech disorder22.12.03.027; 19.19.02.002; 17.02.08.003--Not Available
Stevens-Johnson syndrome10.01.01.045; 23.03.01.007; 11.07.01.005; 12.03.01.014--
Stomatitis07.05.06.005--
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ADReCS-Target
Drug Name ADR Term Target
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