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)
Abdominal pain07.01.05.002--
Alanine aminotransferase increased13.03.04.005--
Albuminuria20.02.01.001---
Altered state of consciousness17.02.04.001; 19.07.01.0030.007424%-
Anaemia01.03.02.001--
Angina pectoris02.02.02.002; 24.04.04.002--
Angina unstable02.02.02.004; 24.04.04.004---
Angioedema10.01.05.009; 22.04.02.008; 23.04.01.0010.007424%-
Arrhythmia02.03.02.0010.011136%-
Arthralgia15.01.02.001--
Aspartate aminotransferase increased13.03.04.011--
Asthenia08.01.01.0010.036378%-
Atrial fibrillation02.03.03.0020.007424%
Back pain15.03.04.005--
Blood cholesterol increased13.12.01.002--
Blood creatine increased13.13.01.001---
Blood creatine phosphokinase increased13.04.01.001--
Blood creatinine increased13.13.01.004--
Blood glucose increased13.02.02.002---
Blood potassium increased13.11.01.011---
Blood sodium decreased13.11.01.012---
Blood triglycerides increased13.12.03.001---
Blood urea increased13.13.01.006---
Blood uric acid increased13.02.04.001---
Body temperature increased13.15.01.001---
Bradycardia02.03.02.0020.014848%-
Breast pain21.05.05.0030.025242%
Bronchitis11.01.09.001; 22.07.01.001--
Cardiac failure02.05.01.0010.011136%
Cardiovascular disorder02.11.01.010; 24.03.02.009---
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ADReCS-Target
Drug Name ADR Term Target
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