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Ergonovine (Ergotrate)

Category:

  • Nervous System

Description:

  • Oxytocic

Indications:

  • Postpartum/postabortal hemorrhage due to uterine atony

Contraindications:

  • Augmentation of labor; administration before delivery of placenta

  • Threatened spontaneous abortion

Precautions:

  • Pregnancy category D; not recommended for routine use prior to delivery of the placenta; may lower prolactin levels, which may decrease lactation

  • Calcium deficiency, prolonged use, hypertension, heart disease

  • Venoarterial shunts, mitral valve stenosis, obliterative vascular disease, sepsis

  • Renal or hepatic disease

Adverse Reactions (Side Effects):

  • CNS: dizziness, fainting, headache

  • CV: chest pain, hypertension

  • EENT: tinnitus

  • GU: cramping

  • MISC: sweating, dyspnea

Dosage:

Administered intramuscularly and intravenously

  • Adult: 

    • IM/IV 0.2mg, severe uterine bleeding may require repeated doses, but rarely more than 0.2mg per 2-4 hours (confine IV route to emergencies)

 


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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