Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Bromocriptine
Drug ID BADD_D00304
Description Bromocriptine mesylate is a semisynthetic ergot alkaloid derivative with potent dopaminergic activity. It is indicated for the management of signs and symptoms of Parkinsonian Syndrome. Bromocriptine also inhibits prolactin secretion and may be used to treat dysfunctions associated with hyperprolactinemia. It also causes sustained suppression of somatotropin (growth hormone) secretion in some patients with acromegaly. Bromocriptine has been associated with pulmonary fibrosis.
Indications and Usage For the treatment of galactorrhea due to hyperprolactinemia, prolactin-dependent menstrual disorders and infertility, prolactin-secreting adenomas, prolactin-dependent male hypogonadism, as adjunct therapy to surgery or radiotherapy for acromegaly or as monotherapy is special cases, as monotherapy in early Parksinsonian Syndrome or as an adjunct with levodopa in advanced cases with motor complications. Bromocriptine has also been used off-label to treat restless legs syndrome and neuroleptic malignant syndrome.
Marketing Status approved; investigational
ATC Code G02CB01; N04BC01
DrugBank ID DB01200
KEGG ID D03165
MeSH ID D001971
PubChem ID 31101
TTD Drug ID D06YFA
NDC Product Code Not Available
UNII 3A64E3G5ZO
Synonyms Bromocriptine | 2-Bromo-alpha-ergokryptine | 2 Bromo alpha ergokryptine | Bromocryptin | 2-Bromoergokryptine | 2 Bromoergokryptine | Bromocriptin | 2-Bromoergocryptine | 2 Bromoergocryptine | 2-Bromo-alpha-ergocryptine | 2 Bromo alpha ergocryptine | CB-154 | CB 154 | CB154 | Parlodel | 2-Bromoergocryptine Mesylate | 2 Bromoergocryptine Mesylate | Mesylate, 2-Bromoergocryptine | Bromocriptine Mesylate | Mesylate, Bromocriptine | 2-Bromoergocryptine Methanesulfonate | 2 Bromoergocryptine Methanesulfonate | Methanesulfonate, 2-Bromoergocryptine
Chemical Information
Molecular Formula C32H40BrN5O5
CAS Registry Number 25614-03-3
SMILES CC(C)CC1C(=O)N2CCCC2C3(N1C(=O)C(O3)(C(C)C)NC(=O)C4CN(C5CC6=C(NC7=CC=CC(=C67)C5=C 4)Br)C)O
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)
Depression19.15.01.0010.001979%
Diarrhoea07.02.01.001--
Disorientation17.02.05.015; 19.13.01.002---
Disturbance in attention17.03.03.001; 19.21.02.0020.001319%
Dizziness02.11.04.006; 17.02.05.003; 24.06.02.0070.001979%
Drug ineffective08.06.01.0060.003298%-
Dry mouth07.06.01.002--
Dyskinesia17.01.02.006--
Dyspepsia07.01.02.001--
Dysphagia07.01.06.0030.001319%
Dyspnoea02.11.05.003; 22.02.01.0040.003298%
Epilepsy17.12.03.002---
Erythromelalgia23.06.05.002; 24.03.01.001---
Face oedema08.01.07.003; 10.01.05.002; 23.04.01.004--
Fatigue08.01.01.002--
Gastrointestinal haemorrhage07.12.02.001; 24.07.02.009---
Hallucination19.10.04.0030.001319%
Hallucination, visual19.10.04.007---
Headache17.14.01.0010.008180%
Hypertension24.08.02.0010.003958%
Hypoaesthesia17.02.06.023; 23.03.03.081---
Hypokalaemia14.05.03.0020.001979%
Hypotension24.06.03.0020.005145%
Insomnia17.15.03.002; 19.02.01.002--
Lethargy08.01.01.008; 17.02.04.003; 19.04.04.004--
Libido increased19.08.03.002; 21.03.02.0070.001319%
Livedo reticularis23.06.05.001; 24.03.04.003---
Loss of consciousness17.02.04.0040.004881%-
Malaise08.01.01.0030.004618%
Migraine17.14.02.001; 24.03.05.0030.001319%-
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