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Electrolyte Pregnancy: May be administered in eclampsia as the condition may be life-threatening to mother and baby. Magnesium crosses the placenta and may produce hypotonia, hyporeflexia and hypotension; given during labour it may cause respiratory depression of the newborn. Monitor fetal heart rate and avoid use within 2 hours of delivery. Continuous administration for more than 5–7 days in pregnancy can cause fetal hypocalcaemia, skeletal demineralisation and osteopenia. Breastfeeding: safety not established — not advisable unless considered essential.

Magnesium Sulphate

Brand names: Magnesium Sulphate 50%

An intravenous magnesium salt (British spelling variant) used in emergencies for eclampsia and severe pre-eclampsia, for ventricular arrhythmias including torsades de pointes, and as add-on therapy in severe or life-threatening acute asthma.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: Prevention of recurrent seizures in eclampsia: loading dose 4 g (16 mmol) of magnesium ions IV (40 ml of a 10% solution) — or in some cases 5 g (20 mmol) of magnesium ions IV (50 ml of a 10% solution) — given over 5–15 minutes, followed by an infusion of 1 g (4 mmol)/hour (10 ml of a 10% solution) continued for 24 hours after the last fit
Route: Intravenous infusion
Frequency: Loading dose over 5–15 minutes, then 1 g (4 mmol)/hour continuous infusion for 24 hours after the last fit
Max: In renal impairment the dosage should not exceed 20 g in 48 hours (200 ml of a 10% solution; 80 mmol of magnesium ions)
SOURCE: UK SPC (eMC) for Magnesium Sulfate 10% w/v solution for infusion, §4.2 (https://www.medicines.org.uk/emc/product/10502/smpc). RECURRENT CONVULSIONS: if convulsions recur, a further 2–4 g (8–16 mmol) of magnesium ions (20–40 ml of a 10% solution, depending on the woman's weight — 2 g (8 mmol) if less than 70 kg) is given IV over 5 minutes. SECOND SPC INDICATION — treatment of magnesium deficiency in hypomagnesaemia: up to 40 g or 160 mmol of magnesium ions (400 ml of a 10% solution) by slow intravenous infusion (in glucose 5%) over up to 5 days may be required to replace the deficit (allowing for urinary losses). TITRATION/MONITORING: dosage should be tailored to the individual patient's needs and responses; plasma magnesium concentrations should be measured to determine the rate and duration of infusion and should be monitored throughout therapy. Serum calcium levels should be routinely monitored. ELDERLY: no special recommendation — use with caution due to the risk of renal impairment in this age group. PAEDIATRIC POPULATION: the SPC states 'No special recommendation' and gives no paediatric regimen. PREGNANCY: fetal heart rate should be monitored and use within 2 hours of delivery should be avoided; continuous administration for more than 5 to 7 days can cause fetal skeletal adverse effects. GAP — this SPC covers only hypomagnesaemia and eclampsia. It does NOT contain the acute severe asthma, torsades de pointes or refractory VF regimens shown on this page; those regimens must be sourced separately (national asthma / resuscitation guidance) and verified by the clinician. For instructions on dilution before administration see SPC §6.6.

Dose adjustments

Renal

Doses must be reduced in renal impairment; caution must be observed to prevent exceeding the renal excretory capacity. The dosage should not exceed 20 g in 48 hours (200 ml of a 10% solution; 80 mmol of magnesium ions). In eclampsia, a suggested dose reduction in severe renal impairment is a maximum of 20 g (80 mmol of magnesium ions) over 48 hours.

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

Side effects

  • Respiratory depression
  • Cardiac arrhythmias, cardiac arrest and ECG changes (prolonged PR, QRS and QT intervals), bradycardia
  • Flushing of the skin and hypotension due to peripheral vasodilatation
  • Loss of tendon reflexes due to neuromuscular blockade, muscle weakness
  • Nausea, vomiting, drowsiness and confusion (features of hypermagnesaemia; coma, slurred speech and double vision with excess)
  • Isolated reports of maternal and fetal hypocalcaemia with high doses

Interactions

  • Non-depolarising muscle relaxants (e.g. tubocurarine) — effects enhanced by parenteral magnesium salts; neuromuscular blocking effects may be additive
  • Nifedipine — profound hypotension was produced in two women given oral nifedipine
  • Digitalis glycosides — administer magnesium salts with caution
  • Aminoglycoside antibacterials — neuromuscular blocking effects may be additive with parenteral magnesium
  • CNS depressants (barbiturates, opiates, general anaesthetics) — additive central depressant effects; dosage of these agents must be carefully adjusted
  • Intravenous calcium will antagonise the effects of magnesium

Clinical monograph

How it works

Magnesium behaves as a natural calcium antagonist and membrane stabiliser, influencing neuromuscular transmission, bronchial and vascular smooth muscle tone and cardiac excitability.

Prescribing in practice

  • Watch closely for magnesium toxicity—diminished or absent reflexes, respiratory depression and hypotension—and keep intravenous calcium available as the rescue treatment.
  • Reduce dose and intensify monitoring in renal impairment because of the risk of accumulation.
  • Give intravenous doses at the recommended controlled rate to avoid flushing, hypotension and bradycardia.

Monitoring

Monitor reflexes, respiratory rate, blood pressure and urine output, checking serum magnesium concentrations in renal impairment or prolonged high-dose therapy.

Counselling the patient

  • A sensation of warmth or flushing during the infusion is expected and usually passes.
  • Report sudden weakness, drowsiness, difficulty breathing or feeling faint to staff straight away.

Evidence & guidelines

Intravenous magnesium sulphate is supported by the Magpie trial for eclampsia and by NICE and resuscitation guidance for eclampsia and torsades de pointes.

Reference: Magpie Trial, Lancet 2002; NICE NG133; UK ALS Guidelines 2021; 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.

📚 MRCEM Revision

Featured in these MRCEM clinical pathways

Magnesium Sulphate is a core drug in the following exam-focused workups on our sister siteReviseMRCEM.

MRCEM Primary / Intermediate / OSCE candidates: each pathway includes exam-style questions, RCEM/NICE citations, and FAQ summaries.