Amrinone
File:Amrinone.svg | |
Systematic (IUPAC) name | |
---|---|
5-amino-3,4'-bipyridin-6(1H)-one | |
Clinical data | |
Pregnancy category |
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Routes of administration | Intravenous |
Legal status | |
Legal status |
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Pharmacokinetic data | |
Bioavailability | n/a |
Protein binding | 10 to 49% |
Metabolism | Hepatic |
Biological half-life | 5 to 8 hours |
Excretion | Renal (63%) and fecal (18%) |
Identifiers | |
CAS Number | 60719-84-8 |
ATC code | C01CE01 (WHO) |
PubChem | CID 3698 |
ChemSpider | 3570 |
Chemical data | |
Formula | C10H9N3O |
Molar mass | 187.198 g/mol[[Script error: No such module "String".]] |
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Amrinone (INN) or inamrinone (USAN, changed in 2000 to prevent confusion with amiodarone[1]), trade name Inocor, is a pyridine phosphodiesterase 3 inhibitor.[2]
Contents
Uses
It is used in the treatment of congestive heart failure.
It has been studied for use before coronary artery bypass surgery.[3]
Actions
Increases cardiac contractility, vasodilator. Acts by inhibiting the breakdown of both cAMP and cGMP by the phosphodiesterase (PDE3) enzyme.
Indications
Short-term management of severe CHF (not used long term because of increased mortality, probably due to heart failure).
Contraindications
Patients with history of hypersensitivity to the drug.
Precautions
May increase myocardial ischemia. Blood pressure, pulse, and EKG should be constantly monitored. Amrinone should only be diluted with normal saline or 1/2 normal saline; no dextrose solutions should be used. Furosemide should not be administered into an IV line delivering Amrinone.
Side effects
Thrombocytopenia, hepatotoxicity, arrhythmia, nausea, and vomiting.
Routes
IV bolus and infusion as described earlier.
Pediatric dosage
Safety in children has not been established.
References
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- ↑ "Amrinone Becomes Inamrinone". USP Quality Review. United States Pharmacopeia. 73. March 2000.
- ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
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