Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Milrinone
Drug ID BADD_D01467
Description Heart failure is a multifactorial condition that affects roughly 1-2% of the adult population. Often the result of long-term myocardial ischemia, cardiomyopathy, or other cardiac insults, heart failure results from an inability of the heart to perfuse peripheral tissues with sufficient oxygen and metabolites, resulting in complex systemic pathologies. Heart failure is underpinned by numerous physiological changes, including alteration in β-adrenergic signalling and cyclic adenosine monophosphate (cAMP) production, which affects the heart's contractile function and cardiac output.[A228323] Milrinone is a second-generation bipyridine phosphodiesterase (PDE) inhibitor created through chemical modification of [amrinone].[A228333] As a PDE-III inhibitor, milrinone results in increased cAMP levels and improves cardiac function and peripheral vasodilation in acute decongested heart failure.[A228338, A11759, A228323, A228333, A228348, L31483] Milrinone was originally synthesized at the Sterling Winthrop Research Institute in the 1980s.[A228333] It was approved by the FDA on December 31, 1987, and was marketed under the trademark PRIMACOR® by Sanofi-Aventis US before being discontinued.[L31483]
Indications and Usage Indicated for the treatment of congestive heart failure.
Marketing Status Prescription; Discontinued
ATC Code C01CE02
DrugBank ID DB00235
KEGG ID D00417
MeSH ID D020105
PubChem ID 4197
TTD Drug ID D0Y9ZE
NDC Product Code 51916-312; 22568-1127; 17404-0017; 63660-0002; 65392-2202
Synonyms Milrinone | Win-47203 | Win 47203 | Win47203 | Primacor | Corotrope | Corotrop | Milrinone Lactate | Lactate, Milrinone
Chemical Information
Molecular Formula C12H9N3O
CAS Registry Number 78415-72-2
SMILES CC1=C(C=C(C(=O)N1)C#N)C2=CC=NC=C2
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)
Anaphylactic shock10.01.07.002; 24.06.02.004--Not Available
Angina pectoris24.04.04.002; 02.02.02.002--
Arrhythmia02.03.02.001--Not Available
Arrhythmia supraventricular02.03.03.001--Not Available
Bronchospasm22.03.01.004; 10.01.03.012--
Chest pain02.02.02.011; 22.02.08.003; 08.01.08.002--Not Available
Dermatitis23.03.04.002--Not Available
Headache17.14.01.001--
Hypokalaemia14.05.03.002--
Hypotension24.06.03.002--
Liver function test abnormal13.03.01.013--Not Available
Patent ductus arteriosus02.08.01.001; 24.03.03.002; 03.07.01.001--Not Available
Rash23.03.13.001--Not Available
Thrombocytopenia01.08.01.002--Not Available
Torsade de pointes02.03.04.005--Not Available
Tremor17.01.06.002--
Ventricular arrhythmia02.03.04.006--
Ventricular extrasystoles02.03.04.007--Not Available
Ventricular fibrillation02.03.04.008--
Ventricular tachycardia02.03.04.010--
Infusion site reaction12.07.05.006; 08.02.05.005--Not Available
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