Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Cabergoline
Drug ID BADD_D00329
Description Cabergoline, an ergot derivative, is a long-acting dopamine agonist and prolactin inhibitor. It is used to treat hyperprolactinemic disorders and Parkinsonian Syndrome. Cabergoline possesses potent agonist activity on dopamine D2 receptors.
Indications and Usage For the treatment of hyperprolactinemic disorders, either idiopathic or due to prolactinoma (prolactin-secreting adenomas). May also be used to manage symptoms of Parkinsonian Syndrome as monotherapy during initial symptomatic management or as an adjunct to levodopa therapy during advanced stages of disease.
Marketing Status Prescription; Discontinued
ATC Code G02CB03; N04BC06
DrugBank ID DB00248
KEGG ID D00987
MeSH ID D000077465
PubChem ID 54746
TTD Drug ID D04EGX
NDC Product Code 40016-011; 49884-673; 14096-153; 50090-3951; 47848-009; 50742-118; 50090-3157; 59762-1005; 50090-5834; 0093-5420
Synonyms Cabergoline | 1-((6-allylergolin-8beta-yl)carbonyl)-1-(3-(dimethylamino)propyl)-3-ethylurea | FCE 21336 | FCE-21336 | Cabaser | Cabaseril | Dostinex | Galastop | Cabergoline Diphosphate | 1-Ethyl-2-(3'-dimethylaminopropyl)-3-(6'-allylergoline-8'-beta-carbonyl)urea diphosphate
Chemical Information
Molecular Formula C26H37N5O2
CAS Registry Number 81409-90-7
SMILES CCNC(=O)N(CCCN(C)C)C(=O)C1CC2C(CC3=CNC4=CC=CC2=C34)N(C1)CC=C
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Vasospasm24.04.02.002--Not Available
Vertigo17.02.12.002; 04.04.01.003--
Vision blurred06.02.06.007; 17.17.01.0100.022020%
Visual acuity reduced17.17.01.011; 06.02.03.0010.044040%
Visual field defect17.17.01.001; 06.02.07.0030.033030%Not Available
Visual impairment06.02.06.0080.044040%Not Available
Vomiting07.01.07.003--
Weight decreased13.15.01.0050.066061%
Weight increased13.15.01.006--
Coronary artery dissection24.02.02.001; 02.02.01.0040.055051%Not Available
Peripheral swelling08.01.03.053; 02.05.04.0150.033030%Not Available
Tumour haemorrhage24.07.01.028; 16.32.03.0080.022020%
Pituitary haemorrhage24.07.04.009; 17.08.01.019; 05.03.04.0050.154142%Not Available
Sudden onset of sleep17.15.04.003--Not Available
Ventricular hypokinesia02.04.02.0130.055051%Not Available
Ejection fraction decreased13.14.02.0030.033030%
Self-injurious ideation19.12.01.0070.022020%Not Available
Central nervous system lesion17.02.10.0110.033030%Not Available
Neural tube defect17.19.02.002; 03.10.02.0030.005744%Not Available
Musculoskeletal stiffness15.03.01.0050.022020%Not Available
Musculoskeletal discomfort15.03.04.001--Not Available
Trisomy 1819.21.06.004; 17.03.07.004; 03.12.01.002; 02.08.01.0030.008617%Not Available
Foetal death18.01.02.003; 08.04.01.0110.005744%
Adnexa uteri pain21.07.04.0060.022020%Not Available
Disturbance in sexual arousal19.08.04.003--Not Available
Insulin-like growth factor decreased13.10.10.0020.022020%Not Available
Drug resistance08.06.01.0050.028722%Not Available
Hot flush24.03.01.005; 21.02.02.001; 08.01.03.027--
Brain neoplasm17.20.01.003; 16.30.01.0030.005744%Not Available
Cardiac disorder02.01.01.003--Not Available
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