The following information is intended to supplement, not substitute for, the expertise and judgment of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that the use of the drug is safe, appropriate, or effective for you. Consult your healthcare professional before taking this drug.
Pronunciation: (mag-NEE-zee-um SUL-fate)
Class: Mineral, Anticonvulsant, Saline Laxative
Magnesium is an important activator of many enzyme systems, and deficits are accompanied by
a variety of functional disturbances. Magnesium has CNS depressant effects; it prevents/controls
seizures by blocking neuromuscular transmission and decreasing the amount of acetylcholine
liberated at end plate by motor nerve impulse. Orally, it attracts/retains water in intestinal lumen,
thereby increasing intraluminal pressure and inducing the urge to defecate.
Approximately 1% to 2% of total body magnesium is in the extracellular fluid space; 30% bound to albumin.
Excreted solely by the kidneys at a rate proportional to the serum concentration and glomerular filtration.
Immediate (IV, when used as an anticonvulsant); 1 h (IM).
30 min (IV, when used as an anticonvulsant); 3 to 4 h (IM).
Indications and Usage
Seizure prevention and control in severe preeclampsia or eclampsia; replacement therapy in
magnesium deficiency, especially in acute hypomagnesemia accompanied by signs of tetany
similar to those observed in hypocalcemia; corrects or prevents hypomagnesemia by addition to
TPN admixture; control hypertension, encephalopathy, and convulsions in children with acute
Treatment of acute exacerbation of severe asthma; treatment of torsades de pointes; paroxysmal
atrial tachycardia; cerebral edema; barium poisoning.
Toxemia of pregnancy during 2 h preceding delivery.
Dosage and Administration
TPN 5 to 8 mEq of magnesium per 1 L of TPN solution. Typical daily intakes range from 10 to 24
TPN 0.25 to 0.6 mEq/kg/day.
Adults Mild hypomagnesemia
IM 1 g (2 mL of undiluted 50% solution) injected every 6 h for 4 doses.
IV / IM As much as 246 mg/kg (0.5 mL/kg of the undiluted 50% solution) may be given within a
period of 4 h if necessary. Alternatively, 5 g (10 mL) can be added to 1 L of dextrose 5% injection
or sodium chloride 0.9% injection for slow IV infusion over a 3-h period. According to American
Heart Association (AHA) guidelines, the recommended dosage is 1 to 2 g IV over 5 to 60 min. If
seizures are present, give 2 g IV over 10 min. Use caution so as not to exceed the renal excretion
Usually a one-time dose.
PO 10 to 15 g.
PO 5 to 10 g.
IM 20 to 40 mg/kg (0.1 to 0.2 mL/kg of a 20% solution) as needed to control seizures. Seizures in Eclampsia/Preeclampsia
IM / IV 10 to 14 g (as a combination of to 5
g of undiluted 50% solution in each buttock and 4 to
5 g IV in 250 mL of dextrose 5% injection or sodium chloride 0.9% injection, or 4 g of magnesium/dextrose 5% injection premixed solution). Alternatively, the initial IV dose of 4 g may be given by diluting the 50% solution to a 10% or 20% solution and the diluted fluid (40 mL of a 10% solution or 20 mL of a 20% solution) may be injected over 3 to 4 minutes. After the initial dose, 1 to 2 g/h by constant IV infusion or IM doses of 4 to 5 g of undiluted 50% solution every 4 h injected into alternate buttocks as needed (max, 30 to 40 g per 24 h and less in anuric patients). Therapy should continue until paroxysms cease. According to American College of Obstetricians and Gynecologists guidelines, the initial dosage is 4 to 6 g (diluted in 100 mL) given IV over 15 to 20 min, followed by a maintenance dosage of 2 g/h continuous IV infusion.
IV 1.2 to 2 g over 20 min according to AHA/American College of Cardiology (ACC) guidelines.
IV 25 to 75 mg/kg (max dose, 2 g) over 20 min every 4 to 6 hours for 3 or 4 doses; repeat as
Barium P soning Adults
IV 1 to 2 g.
IV / intraosseous 25 to 50 mg/kg (max dose, 2 g) over 10 to 20 min every 4 to 6 h for 3 or 4
Paroxysmal Atrial Tachycardia Adults
IV 3 to 4 g (30 to 40 mL of a 10% solutio ) over 30 sec with extreme caution. Use only if simpler
ave failed and there is no evidence of myocardial damage.
Torsades de Pointes Adults IV The following recommendations are according to AHA/ACC guidelines. If torsades de pointes
ciated with cardiac arrest, 1 to 2 g (diluted in 10 mL of dextrose 5% injection) administered
IV/intraosseous over 5 to 20 min. If torsades de pointes is intermittent and not associated
cardiac arrest, dilute 1 to 2 g in 50 to 100 mL of dextrose 5% injection and administer over 5 to 60 min.
IV According to AHA/ACC guidelines, the dosage is 25 to 50 mg/kg (max dose, 2 g)
The dose should be lower and frequent serum magnesium levels must be obtained. Consider
administration only. Not for intradermal, subcutaneous, or intra-arterial
administration. IM administration is painful; avoid if possible.
se flushing, sweating, and warm sensation; avoid if possible.
• Rate of IV injection should generally not exceed 150 mg/min (1.5 mL of a 10%
concentration or 7.5 mL of a 2% concentration or its e
• 50% solution may be administered undiluted to adults if given by deep IM injection.
Rotate injection sites to reduce tissue irritation.
um chloride 0.9% injection or dextrose 5% injection
to a concentration of 20% or less before IV administration or IM administration in infants and children.
• When administering via IV route, use infusion pump. Deliver in separate line and do not
mix with other IV drugs unless compatibility has been established.
• Prior to repeat doses, test for knee-jerk reflexes. If they are absent, no additional
magnesium should be given until reflexes return.
• Incompatibilities: alcohol (in high concentrations), al
alkali hydroxides, arsenates, barium, calcium, clindamycin, heavy metals, hydrocortisone sodium succinate, phosphates, polymyxin B, procaine, salicylates, streptomycin, strontium, tartrates, tetracycline, tobramycin.
ct from freezing. Discard any unused solution. Unused portions of the
the container should be discarded within 24 h of initial use.
aminoglycosides, amphotericin B, cisplatin, cyclosporine, digitalis, diuretics
Drug-induced renal losses of magnesium can occur. Use with caution and closely monitor
Oral magnesium sulfate may decrease the absorption and clinical effect of chloroquine or
eltrombopag. Separate th admi
nistration times of chloroquine and oral magnesium sulfate by 2
to 4 h. Higher doses of chloroquine may be needed. Separate the administration times of eltrombopag and oral magnesium sulfate by at least 4 h.
Neuromuscular blocking agents
Potentiation of neuromuscular blockade; use with caution. Monitor for respiratory depression.
uromuscular blocking agent dose as needed. Be prepared to provide life support.
The risk of neuromuscular blockade and hypotension may be increased. Closely monitor the
clinical response. Be prepared to provide supportive treatment or to discontinue one or both
drugs if needed.
Decreased absorption of nitrofurantoin (oral magnesium). Separate the administration times by as
cillam e effects (oral magnesium). No special precautions are needed.
Decreased absorption of tetracyclines (oral magnesium). Separate the administration times by 3
ression; circulatory collapse; hypotension.
CNS depression; depressed reflexes; flaccid paralysis.
Hypermagnesemia; hypocalcemia with signs of tetany.
Respiratory depression; respiratory paralysis.
Flushing; hypothermia; sweating.
Monitor serum magnesium levels and the patient's clinical status to guide need for continued
dosage. Normal serum concentration is 1.5 to 2.5 or 3 mEq/mL. Effective anticonvulsant serum
levels range from 2.5 or 3 to 7.5 mEq/L (6 mg per 100 mL). Monitor levels hourly for patients with
severe hypomagnesemia until they reach 1.5 mEq/mL, then every 6 to 12 h for the next 24 h. Once stable, obtain the serum concentration daily. Carefully observe respiration and BP during and after administration of IV magnesium. Urine output should be maintained at 100 mL every 4 h. Clinical indications of a safe dosage regimen include the presence of the patellar reflex (knee-jerk) and absence of respiratory depression (approximately 16 or more breaths per minute). When repeated doses of the drug are given parenterally, knee-jerk reflexes should be tested before each dose; if they are absent, no additional magnesium should be given until they return. The strength of the deep tendon reflexes begins to diminish when magnesium levels exceed 4 mEq/L. Reflexes may be absent at magnesium 10 mEq/L, where respiratory paralysis is a potential hazard.
Category A / Category C , depending on manufacturer.
Excreted. The American Academy of Pediatrics classifies magnesium as compatible with breast-
May requ re reduced dosage because of renal impairment.
Use with caution; renal impairment may lead to magnesium intoxication.
Aluminum toxicit Some of these products may contain aluminum that
cluding premature neonates, who receive parenteral levels of aluminum at more than 4
ate aluminum at levels associated with CNS and bone toxicity. Tissue
loading may occur at even lower rates of administration.
Use IV form only for immediate control of life-threatening convulsions.
Administer with caution if flushing and sweating occurs.
Decreased deep tendon reflexes, disappearance of patellar reflex, ECG changes (ie, prolonged
prolonged QRS complex, prolonged QT interval), heart block, hypotension,
• Advise patient that medication will be prepared and administered by a health care
ealth care provider if drowsiness, muscle weakness, sweating,
• Advise patient to mix granules in at least a half glass of water before swallowing and to
atient to mix with ice chips or flavor with lemon or
• Educate patient regarding other measures that may help prevent constipation (eg,
adequate fluid intake, dietary fiber, regular exercise).
• Caution patient that drug is for short- rm laxative u
lead to dehydration and electrolyte imbalance.
• Advise patient to discontinue use and notify heal
unrelieved constipation, rectal bleeding, symptoms of electrolyte imbalance (eg, muscle cramps or pain, weakness, dizziness).
Copyright 2009 Wolters Kluwer Health.
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