Navigation

ergonovine (ergometrine, Ergotrate)

 

Classes: Ergot Derivatives

Dosing and uses of Ergometrine, Ergotrate (ergonovine)

 

Adult dosage forms and strengths

tablet

  • 0.2mg

injection solution

  • 0.2 mg/mL (1) mL

 

Pospartum or Postabortion Hemorrhage

0.2 mg IM; may repeat in 2-4hr; not to exceed 5 doses totaL

Give IV only in emergency because of potential for HTN & CVA

Alternatively, 0.2-0.4 mg PO q6-12hr PRN for 48 hr or until danger of uterine atony has passed; no more than 1 week

Give over >1 minute & monitor Bp

 

Other Indications & Uses

Prevention and treatment of postpartum and postabortion hemorrhage caused by uterine atony or subinvolution

 

Pediatric dosage forms and strengths

Safety and efficacy not established

 

Ergometrine, Ergotrate (ergonovine) adverse (side) effects

Frequency not defined

Dizziness

Headache

Hypertension

Nasal congestion

Nausea and vomiting

Allergic phenomenon including shock

Angina

Arrythmia

Diaphoresis

Diarrhea

Dyspnea

Foul taste

Hallucinations

Hematuria

Hypertensive episode

Leg cramps

Thrombophlebitis

Tinnitus

Water intoxication

 

Warnings

Contraindications

Hypertension, toxemia, pregnancy, hypersensitivity, prolonged use

Cases of threatened spontaneous abortion

Avoid during breast-feeding

 

Cautions

If administered during the second or third stage of labor prior to delivery of the placenta, complications such as captivation of the placenta may occur

In patients with sepsis, hepatic impairment, renal impairment

 

Pregnancy and lactation

Pregnancy category: C

Lactation: excreted in milk; adverse effect on the nursing infant; may inhibit lactation; use not recommended

 

Pregnancy categories

A: Generally acceptable. Controlled studies in pregnant women show no evidence of fetal risk.

B: May be acceptable. Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk.

C: Use with caution if benefits outweigh risks. Animal studies show risk and human studies not available or neither animal nor human studies done.

D: Use in LIFE-THREATENING emergencies when no safer drug available. Positive evidence of human fetal risk.

X: Do not use in pregnancy. Risks involved outweigh potential benefits. Safer alternatives exist.

NA: Information not available.

 

Pharmacology of Ergometrine, Ergotrate (ergonovine)

Mechanism of action

Produces vasoconstriction to increased strength, duration, and frequency of uterine contraction which in turn impedes uterine blood flow; shortens the third stage of labor

 

Pharmacokinetics

Half-Life: 1-5 min (initial phase); 0.5-2 hr (terminal phase)

Plasma peak time: 30 min

Concentration: 3 ng/mL

Duration in uterine effects: 3 hr (IM); 45 min (IV)

Onset: Uterine contractions are usually initiated within 5-15 min following oral administration, within 2-3 min after IM injection, and 1 min following IV injection

Metabolism: Liver

Excretion: Feces

 

Administration

IV Administration

Give IV only in emergency because of potential for HTN & CVA

Give over >1 min & monitor Bp