Amrinone
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Routes of administration | Intravenous |
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Pharmacokinetic data | |
Bioavailability | n/a |
Protein binding | 10 to 49% |
Metabolism | Hepatic |
Elimination half-life | 5 to 8 hours |
Excretion | Renal (63%) and fecal (18%) |
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E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
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Formula | C10H9N3O |
Molar mass | 187.198 g/mol |
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Ongoing Trials on Amrinone at Clinical Trials.gov Clinical Trials on Amrinone at Google
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US National Guidelines Clearinghouse on Amrinone
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Overview
Amrinone (INN) or inamrinone, trade name Inocor, is a type 3 pyridine phosphodiesterase inhibitor. It is used in the treatment of congestive heart failure.
Class: Cardiac inotrope.
Actions: Increases cardiac contractility, vasodilator.
Indications: Short-term management of severe CHF.
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: Reduction in platelets, nausea and vomiting cardiac arrhythmias.
Dosage: 0.75 mg/kg bolus given slowly over 2-3 minute interval followed by maintenance infusion of 2-15 µg/kg/minute.
Routes: IV bolus and infusion as described earlier.
Pediatric Dosage: Safety in children has not been established
Template:Phosphodiesterase inhibitors
Template:Cardiac stimulants excluding cardiac glycosides
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- Phosphodiesterase inhibitors
- Drugs