Methylergometrine Injectable: Dosing and Precautions
Methylergometrine injectable guidance for postpartum haemorrhage due to uterine atony.
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Source reviewed
source date listed on the source page
Guide category
Injectable drugs
Safety boundary
Prescription medicine information for clinician-guided use.
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Therapeutic action
Uterotonic, oxytocic.
Indications
Postpartum haemorrhage due to uterine atony, although oxytocin is preferred for this indication.
Forms and strengths, route of administration
- 0.2 mg in 1 ml ampoule (0.2 mg/ml) for IM injection.
Dose
- Adult: 0.2 mg every 2 to 4 hours if necessary, maximum 1 g.
Contra-indications, adverse effects, precautions
- Do not administer during delivery or labour.
- Do not administer in case of allergy to ergot alkaloids, severe hypertension, pre-eclampsia, eclampsia, or septicaemia.
- Do not combine with another ergot alkaloid.
- Administer with caution to patients with hepatic or renal impairment or ischaemic disorders.
- Do not administer simultaneously with prostaglandins or oxytocin because uterotonic activity is additive.
- May cause gastrointestinal disturbances, headache, paraesthesia, confusion, dizziness, tinnitus, hypertension, peripheral vasoconstriction, and chest pain.
- Monitor combination with metronidazole, azole antifungals, macrolides, protease inhibitors, efavirenz, and fluoxetine due to the risk of ergotism.
- Pregnancy: contraindicated.
- Breast-feeding: avoid.
- Do not confuse with dihydroergotamine, another ergot alkaloid used for different indications.
- Ergometrine is another uterotonic used for the same indications.
Source
MSF Essential drugs practical guidelines (January 2026)
This page combines source-derived medicine reference sections with Kenza editorial context, while leaving out the Storage and Remarks sections from the source batch.
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