Magnesium Sulphate (Obstetric — Eclampsia/Neuroprotection)
Brand names: Magnesium Sulphate (generic)
Intravenous magnesium sulphate used in obstetrics to prevent and treat eclamptic seizures in women with severe pre-eclampsia or eclampsia, and for fetal neuroprotection in anticipated early preterm birth.
Adult dose
Dose adjustments
Doses must be reduced in renal impairment and care taken not to exceed renal excretory capacity — the dosage should not exceed 20 g in 48 hours (200 mL of a 10% solution, or 80 mmol of magnesium ions). A suggested dose reduction in severe renal impairment is a maximum of 20 g (80 mmol of magnesium ions) over 48 hours. Renal failure is a contraindication. Accumulation to toxic levels is particularly likely in impaired renal function.
Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.
Contraindications
- Hypersensitivity to magnesium and its salts
- Renal failure
- Hepatic encephalopathy, hepatic failure
- Parenteral magnesium salts should generally be avoided in patients with heart block
- US labelling additionally lists: heart block or myocardial damage, diabetic coma, and myasthenia gravis
Side effects
- Respiratory depression; decreased respiratory rate progressing to respiratory paralysis in overdose
- Loss of tendon reflexes due to neuromuscular blockade; muscle weakness
- Flushing of the skin and hypotension due to peripheral vasodilatation
- Cardiac arrhythmias, bradycardia, ECG changes (prolonged PR, QRS and QT intervals), cardiac arrest
- Nausea, vomiting, drowsiness, confusion; slurred speech, double vision; coma
- Isolated reports of maternal and fetal hypocalcaemia with high doses; hypersensitivity reactions
Interactions
- Non-depolarising muscle relaxants (e.g. tubocurarine) — effects enhanced by parenteral magnesium salts; neuromuscular blockade may be potentiated and prolonged
- Nifedipine — profound hypotension reported in two women given oral nifedipine
- Digitalis glycosides — administer parenteral magnesium salts with caution
- Aminoglycoside antibacterials — neuromuscular blocking effects may be additive
- CNS depressants (barbiturates, opiates, general anaesthetics) — additive central depressant effects; dosage of these agents must be carefully adjusted
- Intravenous calcium antagonises the effects of magnesium
Clinical monograph
How it works
Magnesium acts as a membrane stabiliser and cerebral vasodilator and modulates NMDA receptor activity, raising the seizure threshold and conferring neuroprotective effects on the preterm fetal brain.
Prescribing in practice
- Magnesium toxicity is the key hazard, progressing from loss of deep tendon reflexes to respiratory depression and cardiac arrest, so administration requires monitoring of reflexes, respiratory rate and urine output, with calcium gluconate available as the antidote.
- It is given by a loading dose followed by a maintenance infusion under close supervision, with dose reduction considered in renal impairment as magnesium is renally cleared.
- Neonates born after recent maternal administration should be observed for hypotonia and respiratory depression.
Monitoring
Monitor deep tendon reflexes, respiratory rate and urine output during the infusion, escalating assessment if signs of toxicity appear.
Counselling the patient
- This medicine is given by drip to prevent fits and, when given early, to help protect a premature baby's brain.
- You may feel flushed, warm or nauseated while it runs.
- Staff will check your reflexes and breathing regularly to keep the dose safe.
Evidence & guidelines
The Magpie trial established magnesium sulphate as the agent of choice for preventing and treating eclampsia, and trial evidence supports its use for fetal neuroprotection in early preterm birth, as reflected in NICE guidance.
Reference: MAGPIE Trial (Magpie Trial Collaboration Group, Lancet 2002); RCOG Green-top 10a (Eclampsia); Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). 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.
- Phenytoin Correction for Albumin / Renal Failure · Drug Dosing
- Pre-eclampsia Risk Assessment · Antenatal
- Modified Obstetric Early Warning Score (MEOWS) · Maternal Deterioration
- HELLP Syndrome Diagnostic Criteria · Hypertensive Disorders
- Pre-eclampsia Risk Screening (NICE NG133) · Obstetric Complications
- Bishop Score (Cervical Ripeness for Induction) · Labour and Delivery
- Paracetamol overdose · TOXBASE/NPIS; MHRA DSU 2012/2024; SNAP regimen (Lancet 2014)
- TCA overdose · TOXBASE/NPIS; AACT/EAPCCT position statements; Resuscitation Council UK ALS
- Opioid overdose · TOXBASE/NPIS; Resuscitation Council UK
- Anticholinergic toxidrome · TOXBASE/NPIS; AACT/EAPCCT
- Benzodiazepine overdose · TOXBASE/NPIS; AACT/EAPCCT
- β-blocker overdose · TOXBASE/NPIS; AACT/EAPCCT; ESC