Milrinone

Table of contents

  • Brand Names
  • Chemistry
  • Pharmacologic Category
  • Mechanism of Action
  • Therapeutic Use
  • Unlabeled Use
  • Pregnancy and Lactation Implications
  • Contraindications
  • Warnings and Precautions
  • Adverse Reactions
  • Genes that may be involved
  • Drug Interactions
  • Dosage
  • Pharmacokinetics and Pharmacodynamics
  • Special Considerations

Brand Names

Europe

Austria: Corotrop; Belgium: Corotrope; Czech Republic: Corotrop; France: Corotrope; Germany: Corotrop; Greece: Corotrope; Hungary: Corotrope; Luxembourg: Corotrope; Malta: Primacor; Netherlands: Corotrope, Milrinon; Poland: Corotrope; Portugal: Corotrope; Romania: Corotrope; Slovakia: Corotrope; Spain: Corotrope; Sweden: Corotrop; UK: Primacor.

North America

Canada: Milrinone; USA: Milrinone, Primacor.

Latin America

Argentina: Corotrope; Brazil: Primacor; Mexico: Primacor.

Asia

Japan: Milrila, Milrinone.

Drug combinations

Chemistry

Milrinone: C~12~H~9~N~3~O. Mw: 211.22. (1) [3,4′-Bipyridine]-5-carbonitrile, 1,6-dihydro-2-methyl-6-oxo-; (2) 1,6-Dihydro-2-methyl-6-oxo[3,4′-bipyridine]-5-carbonitrile. CAS-78415-72-2 (1983).

Pharmacologic Category

Cardiotonic Agents; Phosphodiesterase Enzyme Inhibitor. (ATC-Code: C01CE02).

Mechanism of action

Selective phosphodiesterase inhibitor in cardiac and vascular tissue, resulting in vasodilation and inotropic effects with little chronotropic activity.

Therapeutic use

Short-term intravenous therapy of acutely-decompensated heart failure.

Pregnancy and lactiation implications

Use with caution during pregnancy or lactation.

Unlabeled use

Inotropic therapy for patients unresponsive to other acute heart failure therapies (e.g. dobutamine). Outpatient inotropic therapy for heart transplant candidates. Palliation of symptoms in end-stage heart failure patients who are not transplant candidates.

Contraindications

Hypersensitivity to milrinone, inamrinone, or any component of the formulation. Concurrent use of inamrinone.

Warnings and precautions

Arrhythmias possible; might persist even after discontinuation of therapy, especially in renal dysfunction. Hepatic effects might occur (elevations in LFTs or clinical symptoms of hepatotoxicity). Hypotension might be prolonged, especially in renal dysfunction. Electrolyte imbalances (hypokalemia or hypomagnesemia), should be corrected. Not recommended in acute myocardial infarction treatment. Use with caution in renal impairment (hypotension might be prolonged). Long-term therapy strongly discouraged.

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