Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Selegiline
Drug ID BADD_D02002
Description A selective, irreversible inhibitor of Type B monoamine oxidase. It is used in newly diagnosed patients with Parkinson's disease. It may slow progression of the clinical disease and delay the requirement for levodopa therapy. It also may be given with levodopa upon onset of disability. (From AMA Drug Evaluations Annual, 1994, p385) The compound without isomeric designation is Deprenyl.
Indications and Usage Monotherapy for initial treatment of Parkinson's disease, as well as an adjunct therapy in patients with a decreased response to levodopa/carbadopa. Also used for the palliative treatment of mild to moderate Alzheimer's disease and at higher doses, for the treatment of depression.
Marketing Status approved; investigational; vet_approved
ATC Code N04BD01
DrugBank ID DB01037
KEGG ID D03731
MeSH ID D012642
PubChem ID 26757
TTD Drug ID D0S2UG
NDC Product Code 49502-902; 46438-0642; 49502-901; 42973-349; 49502-900
UNII 2K1V7GP655
Synonyms Selegiline | Selegyline | Selegiline, (R)-Isomer | L-Deprenyl | Emsam | Selegiline Hydrochloride, (R,S)-Isomer | Selegiline Hydrochloride, (S)-Isomer | Eldepryl | Selegiline, (S)-Isomer | Yumex | Jumex | Humex | Zelapar | Deprenyl | E-250 | E 250 | E250 | Selegiline Hydrochloride, (R)-Isomer | Selegiline Hydrochloride | Selegiline, (R,S)-Isomer | Deprenalin | Deprenil
Chemical Information
Molecular Formula C13H17N
CAS Registry Number 14611-51-9
SMILES CC(CC1=CC=CC=C1)N(C)CC#C
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)
Blood disorder01.05.01.004---
Psychotic disorder19.03.01.002--
Pulmonary function test decreased13.19.01.001---
Grimacing17.02.05.029---
Hepatobiliary disease09.01.08.003---
Hyperlipidaemia14.08.03.001--
Cystitis noninfective20.03.02.001--
Chronic kidney disease20.01.03.017--
Vulvovaginal mycotic infection11.03.05.004; 21.14.02.004---
Congenital skin disorder03.05.01.008; 23.07.04.013---
Application site haemorrhage08.02.01.040; 12.07.01.040; 24.07.01.0480.014242%-
Candida infection11.03.03.021--
Depersonalisation/derealisation disorder19.14.01.004---
Parkinsonism hyperpyrexia syndrome08.06.02.018; 17.01.05.0130.014242%-
Dyskinesia hyperpyrexia syndrome17.01.02.0280.006474%-
Gait inability08.01.02.011; 17.02.05.0690.014242%-
Heavy menstrual bleeding21.01.03.005---
Intermenstrual bleeding21.01.01.015---
Therapeutic product effect decreased08.06.01.0500.044021%-
Vulvovaginal inflammation21.14.02.014---
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