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 Prescription; Discontinued
ATC Code C03DA04
DrugBank ID DB00700
KEGG ID D01115
MeSH ID D000077545
PubChem ID 443872
TTD Drug ID D0Q4SD
NDC Product Code 51991-877; 69367-307; 71216-3011; 16729-294; 71205-864; 60687-451; 70436-098; 16729-293; 70436-099; 46014-1102; 70966-0033; 16812-001; 0025-1720; 0025-1710; 71216-3010; 71205-863; 66993-343; 42291-454; 59762-1720; 68554-0116; 14501-0007; 42291-455; 59762-1710; 0378-1031; 66993-344; 51991-878; 73309-095; 0185-5368; 0009-5276; 69367-308; 0185-5369; 0378-1030
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
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)
Abdominal pain07.01.05.002--
Acute prerenal failure20.01.03.001; 24.06.02.0030.034027%Not Available
Alanine aminotransferase increased13.03.01.003--
Albuminuria20.02.01.001--Not Available
Altered state of consciousness19.07.01.003; 17.02.04.0010.034027%Not Available
Anaemia01.03.02.001--
Angina pectoris24.04.04.002; 02.02.02.002--
Angina unstable24.04.04.004; 02.02.02.004--Not Available
Angioedema23.04.01.001; 10.01.05.009--Not Available
Arthralgia15.01.02.001--
Aspartate aminotransferase increased13.03.01.006--
Asthenia08.01.01.0010.068055%Not Available
Atrial fibrillation02.03.03.002--
Back pain15.03.04.005--
Blood cholesterol increased13.12.01.002--
Blood creatine increased13.13.01.001--Not Available
Blood creatine phosphokinase increased13.04.01.001--
Blood creatinine increased13.13.01.0040.008877%
Blood glucose increased13.02.02.002--Not Available
Blood potassium increased13.11.01.0110.034027%Not Available
Blood pressure decreased13.14.03.0020.008877%Not Available
Blood sodium decreased13.11.01.012--Not Available
Blood triglycerides increased13.12.03.001--Not Available
Blood urea increased13.13.01.006--Not Available
Blood uric acid increased13.02.04.001--Not Available
Body temperature increased13.15.01.001--Not Available
Bradycardia02.03.02.0020.051041%Not Available
Breast pain21.05.05.0030.034027%
Bronchitis22.07.01.001; 11.01.09.001--
Cardiac failure02.05.01.0010.008877%
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