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Dobutamine (Dobutrex)

Category:

  • Nervous system

Description:

  • Sympathomimetic

Indications:

  • Short-term treatment of adults with cardiac decompensation due to depressed myocardial contractility

Contraindications:

  • Hypertrophic cardiomyopathy

  • Uncontrolled atrial fibrillation or flutter (unless a digitalis preparation is used prior to starting therapy with dobutamine)

Precautions:

  • Pregnancy category C; excreted in breast milk

  • Children, hypertension, sulfite sensitivity

Adverse Reactions (Side Effects):

  • CNS: anxiety, dizziness, headache, paresthesia

  • CV: angina, dysrhythmia, hypertension, palpitations, PVC’s, tachycardia

  • GI: heartburn, nausea, vomiting,

  • METAB: hypokalemia

  • MS: leg cramps

Dosage:

Administered intravenously

  • Adult:   

    • IV INF 2.5-15 mcg/kg/min

    • maximum dose 40 mcg/kg/min

Special Consideration:

  •  Sodium bicarbonate: alkalinizing substances inactivate dobutamine

 


The information contained here is an abbreviated summary. For more detailed and complete information, consult the manufacturer's product information sheets or standard textbooks

Source: Operational Medicine 2001,  Health Care in Military Settings, NAVMED P-5139, May 1, 2001, Bureau of Medicine and Surgery, Department of the Navy, 2300 E Street NW, Washington, D.C., 20372-5300

This information is provided by The Brookside Associates.  The Brookside Associates, LLC. is a private organization, not affiliated with any governmental agency. The opinions presented here are those of the author and do not necessarily represent the opinions of the Brookside Associates or the Department of Defense. The presence of any advertising on these pages does not constitute an endorsement of that product or service by either the US Department of Defense or the Brookside Associates. All material presented here is unclassified.

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