Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Eplerenone
Drug ID BADD_D00786
Description Eplerenone, an aldosterone receptor antagonist similar to spironolactone, has been shown to produce sustained increases in plasma renin and serum aldosterone, consistent with inhibition of the negative regulatory feedback of aldosterone on renin secretion. The resulting increased plasma renin activity and aldosterone circulating levels do not overcome the effects of eplerenone. Eplerenone selectively binds to recombinant human mineralocorticoid receptors relative to its binding to recombinant human glucocorticoid, progesterone and androgen receptors.
Indications and Usage For improvement of survival of stable patients with left ventricular systolic dysfunction (ejection fraction <40%) and clinical evidence of congestive heart failure after an acute myocardial infarction.
Marketing Status approved
ATC Code C03DA04
DrugBank ID DB00700
KEGG ID D01115
MeSH ID D000077545
PubChem ID 443872
TTD Drug ID D0Q4SD
NDC Product Code 16637-0060; 63629-9414; 69367-307; 31722-050; 42291-455; 71205-864; 70966-0033; 71216-3010; 42291-454; 59762-1720; 70436-098; 71205-863; 60687-451; 73309-095; 16729-293; 0185-5369; 51991-878; 0025-1710; 0025-1720; 69367-308; 14501-0007; 31722-049; 16812-001; 46014-1102; 73320-004; 68554-0116; 59762-1710; 66993-343; 70436-099; 0009-5276; 16729-294; 51991-877; 66993-344; 73320-005; 0185-5368
UNII 6995V82D0B
Synonyms Eplerenone | Eplerenon | Inspra | 9,11-Epoxy-7-(methoxycarbonyl)-3-oxo-17-pregn-4-ene-21,17-carbolactone
Chemical Information
Molecular Formula C24H30O6
CAS Registry Number 107724-20-9
SMILES CC12CCC(=O)C=C1CC(C3C24C(O4)CC5(C3CCC56CCC(=O)O6)C)C(=O)OC
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)
Renal failure20.01.03.0050.025985%-
Rhabdomyolysis15.05.05.0020.007424%
Shock24.06.02.002---
Skin disorder23.03.03.007---
Sudden death02.03.04.013; 08.04.01.0030.007424%
Swelling08.01.03.0150.016333%-
Syncope02.11.04.015; 17.02.04.008; 24.06.02.0120.007424%
Tinnitus04.04.01.002; 17.04.07.004--
Upper respiratory tract infection11.01.13.009; 22.07.03.011--
Urethral disorder20.07.01.002---
Urinary tract disorder20.08.01.001---
Urinary tract infection11.01.14.004; 20.08.02.001--
Urine abnormality20.02.01.013---
Urticaria10.01.06.001; 23.04.02.0010.007424%
Vaginal haemorrhage21.08.01.001; 24.07.03.005--
Ventricular arrhythmia02.03.04.006--
Ventricular tachycardia02.03.04.010--
Vomiting07.01.07.003--
General physical health deterioration08.01.03.0180.007424%-
Blood pressure inadequately controlled24.06.01.0070.020045%-
Acute coronary syndrome02.02.02.015; 24.04.04.011---
Lymphatic disorder01.09.01.003---
Protein urine present13.13.02.006---
Musculoskeletal discomfort15.03.04.001---
Haemorrhage24.07.01.0020.007424%-
Cognitive disorder17.03.03.003; 19.21.02.0010.007424%
Disturbance in sexual arousal19.08.04.003---
Angiopathy24.03.02.007---
Cardiac disorder02.11.01.0030.049000%-
Connective tissue disorder10.04.04.026; 15.06.01.006---
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ADReCS-Target
Drug Name ADR Term Target
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