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Electrolyte / Anticonvulsant / Tocolytic 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 (IV — ICU/Anaesthesia)

Brand names: MgSO4, Magnesium Sulphate 50%

Intravenous magnesium sulphate is used for eclampsia and severe pre-eclampsia (seizure treatment and prevention), for severe or life-threatening acute asthma, and for torsades de pointes.

Adult dose

Dose: 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)
Route: Intravenous infusion
Frequency: Slow intravenous infusion over up to 5 days; rate and duration determined by measured plasma magnesium concentrations
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). SECOND SPC INDICATION — prevention of recurrent seizures in eclampsia: a loading dose of 4 g (16 mmol) of magnesium ions IV (40 ml of a 10% solution), or in some cases 5 g (20 mmol; 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. 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. 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 monitored throughout therapy; serum calcium levels should be routinely monitored. Respiratory depression may occur — caution in patients with respiratory disease; caution in myasthenia gravis (risk of myasthenic crisis). 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. GAP — this SPC covers only hypomagnesaemia and eclampsia. It does NOT contain the torsades de pointes or severe asthma regimens shown on this page, and it states no per-mmol bolus regimen (e.g. 8 mmol/2 g over 10–15 min) for hypomagnesaemia; those must be sourced separately and verified by the clinician. Note the SPC product is a 10% w/v solution. 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). Especially in patients with impaired renal function there may be sufficient accumulation to produce toxic effects.

Dose independently re-sourced from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — clinician-reviewed. 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, confusion; coma, slurred speech and double vision with excess magnesium
  • Electrolyte/fluid abnormalities (hypophosphataemia, hyperosmolar dehydration); 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
  • Neuromuscular blocking agents and CNS depressants — effects may be enhanced by parenteral magnesium
  • Aminoglycoside antibacterials — neuromuscular blocking effects may be additive with parenteral magnesium
  • Barbiturates, opiates, general anaesthetics and other CNS depressants — additive central depressant effects; their dosage must be carefully adjusted
  • Nifedipine — profound hypotension was produced in two women given oral nifedipine
  • Digitalis glycosides — administer magnesium salts with caution
  • Intravenous calcium will antagonise the effects of magnesium

Clinical monograph

How it works

Magnesium acts as a membrane stabiliser and physiological calcium antagonist, with anticonvulsant, bronchodilator and antiarrhythmic effects and cerebral vasodilatation relevant to eclampsia.

Prescribing in practice

  • Watch for magnesium toxicity — loss of deep tendon reflexes is an early warning sign, progressing to respiratory depression, hypotension and ultimately cardiac arrest.
  • Reduce the dose and monitor more closely in renal impairment, as magnesium is renally cleared and accumulates.
  • Have intravenous calcium available as the antidote for significant magnesium toxicity.

Monitoring

Monitor deep tendon reflexes, respiratory rate, blood pressure and conscious level during and after infusion (with urine output in pre-eclampsia), and check magnesium levels where toxicity is suspected or renal function is impaired.

Counselling the patient

  • Brief the team to check reflexes and respiratory rate regularly and to stop the infusion if reflexes are lost or breathing is depressed.
  • Warn that a warm, flushed feeling during infusion is common, but breathlessness or marked weakness must be reported at once.
  • Ensure intravenous calcium is to hand as the antidote, especially in renal impairment.

Evidence & guidelines

Recommended for eclampsia and severe pre-eclampsia (NICE NG133), severe acute asthma (BTS/SIGN; NICE) and torsades de pointes (Resuscitation Council UK).

Reference: Magpie Trial (Lancet 2002); NICE NG133 (Hypertension in Pregnancy); 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.