- September 13, 2022
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Brand Name :
Ergotab, Ergotrate, Ergoto, Erinmet, Evina, Metregina, Malergo, Mitrotan
Synonyms :
ergonovine
Class :
Uterine stimulants; ergot alkaloids
Brand Name :
Ergotab, Ergotrate, Ergoto, Erinmet, Evina, Metregina, Malergo, Mitrotan
Synonyms :
ergonovine
Class :
Uterine stimulants; ergot alkaloids
Dosage Forms & Strengths
Injectable solution
0.25 mg/ml
0.2 mg intramuscularly
In the case of an emergency where excessive bleeding from the uterus occurs, 0.2 mg through an intravenous route is administered
The intravenous dose is administered for at least 1 minute; uterine contractions and blood pressure should be monitored carefully
A total of 5 doses can be repeated every 2-4 hours as required
Additional Comments
The intravenous dose should be diluted with 5 ml of normal saline before administration
Patients who are calcium deficient may not respond to the drug; for them, cautious calcium administration is advised
Not recommended for pediatrics
Refer to the adult dosing
acrivastine and pseudoephedrine
may increase the vasoconstrictive effect of alpha/beta agonists
may decrease the vasodilatory effect when combined with nitroglycerin
they increase the effect of vasoconstriction of alpha-1 agonists
may increase the vasoconstriction effect
may increase the vasoconstriction effect
may increase the vasoconstriction effect
may increase the vasoconstriction effect
may increase the vasoconstriction effect
reverse transcriptase inhibitors increase the concentration of ergonovine in the serum
reverse transcriptase inhibitors increase the concentration of ergonovine in the serum
reverse transcriptase inhibitors increase the concentration of ergonovine in the serum
reverse transcriptase inhibitors increase the concentration of ergonovine in the serum
reverse transcriptase inhibitors increase the concentration of ergonovine in the serum
may have an increased vasoconstricting effect when combined with ergot derivatives
may have an increased vasoconstricting effect when combined with ergot derivatives
may have an increased vasoconstricting effect when combined with ergot derivatives
may have an increased vasoconstricting effect when combined with ergot derivatives
may have an increased vasoconstricting effect when combined with ergot derivatives
may have an increased vasoconstricting effect when combined with alpha1-agonists
may enhance the vasoconstricting effect of ergot Derivatives
may enhance the vasoconstricting effect of ergot Derivatives
may enhance the vasoconstricting effect of ergot Derivatives
may enhance the vasoconstricting effect of ergot Derivatives
may enhance the vasoconstricting effect of ergot Derivatives
may increase the vasoconstriction effect of sympathomimetic drugs
may increase the vasoconstriction effect of sympathomimetic drugs
may enhance the serum concentration of CYP3A4 inhibitors
may enhance the serum concentration of CYP3A4 inhibitors
may increase the levels of serum concentration of ergot derivatives
may increase the levels of serum concentration of ergot derivatives
may increase the levels of serum concentration of ergot derivatives
may increase the levels of serum concentration of ergot derivatives
may increase the levels of serum concentration of ergot derivatives
may increase the levels of serum concentration of ergot derivatives
may increase the vasoconstricting effect of Serotonin 5-HT1D Receptor Agonists (Triptans)
ergot Derivatives may enhance the serotonergic effect of serotonergic Agents
Beta-Blockers increase the effect of vasoconstriction of ergot derivatives
Beta-Blockers increase the effect of vasoconstriction of ergot derivatives
Beta-Blockers increase the effect of vasoconstriction of ergot derivatives
Beta-Blockers increase the effect of vasoconstriction of ergot derivatives
Beta-Blockers increase the effect of vasoconstriction of ergot derivatives
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may increase the levels of serum concentration
may decrease the levels of serum concentration
may decrease the levels of serum concentration
may decrease the levels of serum concentration
may decrease the levels of serum concentration
may decrease the levels of serum concentration
may decrease the levels of serum concentration
may decrease the levels of serum concentration
may decrease the levels of serum concentration
may decrease the levels of serum concentration
it may increase the effect of serotonergic agents
beta-blockers may enhance the vasoconstricting effect of ergot derivatives
beta-blockers may enhance the vasoconstricting effect of ergot derivatives
beta-blockers may enhance the vasoconstricting effect of ergot derivatives
beta-blockers may enhance the vasoconstricting effect of ergot derivatives
beta-blockers may enhance the vasoconstricting effect of ergot derivatives
may increase the serum concentration of ergot derivatives
may increase the serum concentration of ergot derivatives
may increase the serum concentration of ergot derivatives
may increase the serum concentration of ergot derivatives
may increase the serum concentration of ergot derivatives
may increase the vasoconstrictive effect of beta blockers
may increase the effect of ergot derivatives
may increase the effect of ergot derivatives
may increase the effect of ergot derivatives
may increase the effect of ergot derivatives
may increase the effect of ergot derivatives
may increase the effect of ergot derivatives
may increase the vasoconstricting effect
may increase the vasoconstricting effect
may increase the vasoconstricting effect
may increase the vasoconstricting effect
may increase the vasoconstricting effect
may increase the vasoconstricting effect
may increase the vasoconstricting effect
may increase the serum concentration
may increase the serum concentration
may increase the serum concentration
may increase the serum concentration
may increase the serum concentration
may increase the serum concentration
may increase the vasoconstricting effect
Actions and Spectrum:
ergonovine is a medication that is used for a variety of purposes, including treating certain types of headaches, preventing bleeding after childbirth, and stimulating uterine contractions during labor. It is a type of ergot alkaloid, which means that it is derived from the ergot fungus.
The primary action of ergonovine is to stimulate the smooth muscle tissue in the body, including the smooth muscle in the blood vessels and uterus. It works by binding to and activating specific receptors in these tissues, which leads to their contraction.
In the blood vessels, ergonovine causes vasoconstriction, which means that the blood vessels narrow and the blood flow through them is reduced.
In the uterus, ergonovine can cause strong, coordinated contractions, which can be useful during labor to help promote the progress of childbirth. It can also be used after childbirth to help prevent excessive bleeding by causing the uterus to contract.
Frequency not Defined
Peripheral vasospasm
Gangrene
Palpitation
Vasoconstriction
Bradycardia
Thrombophlebitis
Ventricular arrhythmias
Chest pain
Diarrhea
Vomiting
Nausea
Abdominal Pain
Esophageal spasm
Hypertension
Headache
Dizziness
Skin rashes
Diaphoresis
Dyspnea
Pleural thickening
Leg cramps
Hallucinations
Abnormal liver functioning
Black Box Warning:
The black box warning for ergonovine states that the medication should not be used to induce labor in women with a history of cardiovascular disease, including hypertension, preeclampsia, and eclampsia.
This is because ergonovine can cause constriction of the blood vessels, that leads to decrease in blood flow causing a heart attack, stroke, and death.
Contraindication/Caution:
Contraindications:
Caution:
Pregnancy consideration:
Category X
Breastfeeding warnings:
Lactating mothers should not breastfeed during the therapy
Pregnancy category:
Pharmacology:
ergonovine works by binding to and activating specific receptors in smooth muscle cells, leading to their contraction. It has a high affinity for the serotonin receptor subtype 5-HT2A, as well as for alpha-adrenergic receptors. The activation of these receptors causes vasoconstriction, leading to decreased blood flow through the vessels. In the uterus, ergonovine causes strong, coordinated contractions, leading to its use during labor to help promote the progress of childbirth.
Pharmacodynamics:
Effect on Uterine Contraction: ergonovine has a direct stimulatory effect on the smooth muscle of the uterus, causing strong and coordinated contractions. The medication increases the tone and frequency of uterine contractions, leading to the progress of labor. It is particularly useful in cases of postpartum hemorrhage, where it can help to prevent excessive bleeding by promoting uterine contractions.
Effect on Blood Vessels: ergonovine causes vasoconstriction by activating alpha-adrenergic receptors and 5-HT2A receptors in the smooth muscle cells of the blood vessels. This can lead to decreased blood flow through the vessels, which can be useful in the treatment of certain types of headaches, such as migraines. However, excessive vasoconstriction can also lead to serious complications such as heart attack, stroke, and tissue damage.
Pharmacokinetics:
Absorption
ergonovine is administered orally, intravenously, or intramuscularly. After oral administration, ergonovine is rapidly and completely absorbed from the gastrointestinal tract. Peak plasma concentrations are reached within 30 minutes to 2 hours after oral administration.
Distribution
ergonovine is widely distributed throughout the body, with a volume of distribution of about 1.5 L/kg. It is highly bound to plasma proteins, with a protein binding of more than 90%.
Metabolism
ergonovine is primarily metabolized in the liver by cytochrome P450 enzymes, particularly CYP3A4. The major metabolite of ergonovine is 6-methylergometrine, which is less active than the parent drug.
Elimination
ergonovine and its metabolites are excreted mainly in the urine, with a half-life of about 2 hours. The clearance of ergonovine is reduced in patients with liver disease.
Administration:
ergonovine is usually administered as an oral tablet, an injection, or an intrauterine device. The dosage and route of administration depend on the condition being treated and the response of the patient to the medication.
Patient information leaflet
Generic Name: ergonovine
Pronounced: er-goe-NOE-veen
Why do we use ergonovine?
ergonovine is used for several medical purposes, including the prevention and treatment of excessive bleeding after childbirth and the treatment of migraines. Here are some of the reasons why ergonovine is used: