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1 May 2026Injectable drugs

Methylergometrine injectable

Methylergometrine injectable guidance for postpartum haemorrhage due to uterine atony.

Prescription under medical supervision
This guide page is for structured reference only and does not replace a clinician, pharmacist, or emergency review. Dose choice, route choice, interactions, and safety decisions still need professional judgment.

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 reproduces the structured reference information for this batch while leaving out the Storage and Remarks sections.

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