Carbetocin
Brand names: Pabal, Duratocin
Carbetocin is a long-acting synthetic analogue of oxytocin used to prevent uterine atony and postpartum haemorrhage following delivery.
Adult dose
Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.
Contraindications
- During pregnancy and labour before delivery of the infant
- Must not be used for the induction of labour
- Hypersensitivity to carbetocin, oxytocin or to any of the excipients
- Hepatic or renal disease
- Serious cardiovascular disorders
- Epilepsy
Side effects
- Nausea, abdominal pain (very common); vomiting, metallic taste (common) - IV administration
- Headache, tremor (very common); dizziness (common)
- Hypotension, flushing
- Pruritus
- Feeling of warmth, chills, pain
Interactions
- No drug interactions identified during clinical trials with analgesics, spasmolytics and agents used for epidural or spinal anaesthesia; specific interaction studies not undertaken
- As carbetocin is closely related to oxytocin, oxytocin-associated interactions cannot be excluded: severe hypertension reported when oxytocin given 3-4 hours after prophylactic vasoconstrictor with caudal-block anaesthesia
- With ergot-alkaloids (e.g. methylergometrine), oxytocin and carbetocin may enhance the blood pressure raising effect
Clinical monograph
How it works
It binds oxytocin receptors on uterine smooth muscle, producing sustained uterine contraction and tone to reduce postpartum bleeding.
Prescribing in practice
- It is given as a single dose for prevention of postpartum haemorrhage and must not be used to induce or augment labour or before delivery of the baby.
- It should be used with caution in women with cardiovascular disease, pre-eclampsia, or eclampsia, and is not recommended in significant hepatic or renal impairment.
- Because of its long duration of action, the effect cannot be stopped once administered, unlike a titratable oxytocin infusion.
Monitoring
Monitor uterine tone, blood pressure, and vaginal blood loss after administration.
Counselling the patient
- Explain that this single injection helps the womb contract after birth to reduce the risk of heavy bleeding.
- Report any feeling of faintness, palpitations, or excessive bleeding to the maternity team.
- It is given by a healthcare professional immediately after delivery.
Evidence & guidelines
Uterotonics for active management of the third stage of labour are recommended by NICE to reduce the risk of postpartum haemorrhage.
Reference: RCOG GTG 52; NICE NG235; WHO PPH; SmPC; Confirm identity and dosing against the manufacturer SPC (eMC) and NICE. Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- Spinal Anaesthesia Hypotension Management · AAGBI; ASA
- Pre-Eclampsia / Eclampsia in ED · NICE NG133; RCOG Green-top 10A
- Suspected Ectopic Pregnancy · NICE NG126; RCOG Green-top 21
- Polycystic Ovary Syndrome (PCOS) · International PCOS Guideline 2023; NICE CKS
- Pre-eclampsia Management · NICE NG133 2019
- Ectopic Pregnancy · NICE CG154 / RCOG GTG 21