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Magnesium oxide: Drug information

Magnesium oxide: Drug information
(For additional information see "Magnesium oxide: Patient drug information" and see "Magnesium oxide: Pediatric drug information")

For abbreviations, symbols, and age group definitions used in Lexicomp (show table)
Brand Names: US
  • Mag-200 [OTC];
  • Mag-Oxide [OTC];
  • Magnesium Oxide 400 [OTC] [DSC];
  • MAGnesium-Oxide [OTC];
  • Maox [OTC];
  • Uro-Mag [OTC] [DSC]
Pharmacologic Category
  • Electrolyte Supplement, Oral;
  • Magnesium Salt
Dosing: Adult
Antacid

Antacid (dosage in terms of magnesium oxide salt): OTC labeling: Oral: 1 tablet (400 mg) twice daily; maximum: 2 tablets (800 mg)/24 hours.

Dietary supplement

Dietary supplement (dosage in terms of magnesium oxide salt): OTC labeling: Oral: 1 to 2 tablets (400 to 800 mg) daily; maximum: 2 tablets (800 mg)/24 hours.

Dosing: Kidney Impairment: Adult

There are no dosage adjustments provided in the manufacturer's labeling; however, magnesium is renally excreted. Use with caution; accumulation in renal impairment may lead to magnesium toxicity.

Dosing: Hepatic Impairment: Adult

There are no dosage adjustments provided in the manufacturer's labeling.

Dosing: Pediatric

(For additional information see "Magnesium oxide: Pediatric drug information")

Note: 400 mg magnesium oxide = 241.3 mg elemental magnesium = 19.86 mEq elemental magnesium = 9.93 mmol elemental magnesium.

Hypomagnesemia

Hypomagnesemia: Limited data available: Infants, Children, and Adolescents: Dose expressed as elemental magnesium: Oral: 10 to 20 mg/kg/dose up to 4 times daily; usual adult dose: 300 mg 4 times daily (Anderson 2021; Gal 2007). Note: Achieving optimal magnesium levels using oral therapy may be difficult due to the propensity for magnesium to cause diarrhea: IV replacement may be more appropriate, particularly in situations of severe deficit.

Dosing: Kidney Impairment: Pediatric

There are no dosage adjustments provided in the manufacturer's labeling; however, magnesium is renally excreted. Use with caution; accumulation in renal impairment may lead to magnesium toxicity.

Dosing: Hepatic Impairment: Pediatric

There are no dosage adjustments provided in the manufacturer's labeling.

Dosing: Older Adult

Refer to adult dosing.

Dosage Forms: US

Excipient information presented when available (limited, particularly for generics); consult specific product labeling. [DSC] = Discontinued product

Capsule, Oral:

Uro-Mag: 140 mg [DSC]

Packet, Oral:

Magnesium Oxide 400: 240 mg (80 ea [DSC])

Tablet, Oral:

Mag-200: 200 mg [contains para-aminobenzoic acid]

MAGnesium-Oxide: 400 mg [contains soy polysaccarides]

Maox: 420 mg [contains fd&c yellow #5 (tartrazine)]

Generic: 100 mg, 400 mg, 420 mg, 420 (252 Mg) MG

Tablet, Oral [preservative free]:

Mag-Oxide: 200 mg [corn free, gluten free, no artificial color(s), no artificial flavor(s), starch free, sugar free, wheat free, yeast free]

Generic: 400 mg [DSC], 500 mg

Generic Equivalent Available: US

May be product dependent

Dosage Forms Considerations

400 mg magnesium oxide = elemental magnesium 241.3 mg = magnesium 19.86 mEq = magnesium 9.93 mmol

Administration: Adult

Oral: Administer (preferably with food) at least 2 hours apart from other medications.

Administration: Pediatric

Oral: Administer at least 2 hours apart from other medications.

Use: Labeled Indications

Dietary supplement; antacid: Dietary magnesium supplement; relief of acid indigestion and upset stomach

Adverse Reactions

The following adverse drug reactions and incidences are derived from product labeling unless otherwise specified.

Frequency not defined: Gastrointestinal: Diarrhea (excessive oral doses)

Warnings/Precautions

Disease-related concerns:

• Acid indigestion/upset stomach (self-medication, OTC use): Appropriate use: For occasional use only; serious side effects may occur with prolonged use. For use only under the supervision of a physician in patients with kidney dysfunction or who are pregnant or breast-feeding. Unless directed by a physician, do not use for >2 weeks or exceed the recommended daily dose.

• Renal impairment: Use with caution in patients with renal impairment; accumulation of magnesium may lead to magnesium intoxication.

Warnings: Additional Pediatric Considerations

Multiple salt forms of magnesium exist; pay close attention to the salt form when ordering and administering magnesium; incorrect selection or substitution of one salt for another without proper dosage adjustment may result in serious over- or underdosing.

Metabolism/Transport Effects

None known.

Drug Interactions

Note: Interacting drugs may not be individually listed below if they are part of a group interaction (eg, individual drugs within “CYP3A4 Inducers [Strong]” are NOT listed). For a complete list of drug interactions by individual drug name and detailed management recommendations, use the Lexicomp drug interactions program by clicking on the “Launch drug interactions program” link above.

Alfacalcidol: May increase the serum concentration of Magnesium Salts. Management: Consider using a non-magnesium-containing antacid or phosphate-binding product in patients also receiving alfacalcidol. If magnesium-containing products must be used with alfacalcidol, serum magnesium concentrations should be monitored closely. Risk D: Consider therapy modification

Alpha-Lipoic Acid: Magnesium Salts may decrease the absorption of Alpha-Lipoic Acid. Alpha-Lipoic Acid may decrease the absorption of Magnesium Salts. Management: Separate administration of alpha-lipoic acid from that of any magnesium-containing compounds by several hours. If alpha-lipoic acid is given 30 minutes before breakfast, then administer oral magnesium-containing products at lunch or dinner. Risk D: Consider therapy modification

Baloxavir Marboxil: Polyvalent Cation Containing Products may decrease the serum concentration of Baloxavir Marboxil. Risk X: Avoid combination

Bictegravir: Polyvalent Cation Containing Products may decrease the serum concentration of Bictegravir. Management: Administer bictegravir under fasting conditions at least 2 hours before or 6 hours after polyvalent cation containing products. Coadministration of bictegravir with or 2 hours after most polyvalent cation products is not recommended. Risk D: Consider therapy modification

Bisphosphonate Derivatives: Polyvalent Cation Containing Products may decrease the serum concentration of Bisphosphonate Derivatives. Management: Avoid administration of oral medications containing polyvalent cations within: 2 hours before or after tiludronate/clodronate/etidronate; 60 minutes after oral ibandronate; or 30 minutes after alendronate/risedronate. Risk D: Consider therapy modification

Cabotegravir: Polyvalent Cation Containing Products may decrease the serum concentration of Cabotegravir. Management: Administer polyvalent cation containing products at least 2 hours before or 4 hours after oral cabotegravir. Risk D: Consider therapy modification

Calcitriol (Systemic): May increase the serum concentration of Magnesium Salts. Management: Consider using a non-magnesium-containing antacid or phosphate-binding product in patients also receiving calcitriol. If magnesium-containing products must be used with calcitriol, serum magnesium concentrations should be monitored closely. Risk D: Consider therapy modification

Calcium Polystyrene Sulfonate: Laxatives (Magnesium Containing) may enhance the adverse/toxic effect of Calcium Polystyrene Sulfonate. More specifically, concomitant use of calcium polystyrene sulfonate with magnesium-containing laxatives may result in metabolic alkalosis or with sorbitol may result in intestinal necrosis. Management: Avoid concomitant use of calcium polystyrene sulfonate (rectal or oral) and magnesium-containing laxatives. Risk X: Avoid combination

Deferiprone: Polyvalent Cation Containing Products may decrease the serum concentration of Deferiprone. Management: Separate administration of deferiprone and oral medications or supplements that contain polyvalent cations by at least 4 hours. Risk D: Consider therapy modification

Dolutegravir: Magnesium Salts may decrease the serum concentration of Dolutegravir. Management: Administer dolutegravir at least 2 hours before or 6 hours after oral magnesium salts. Administer the dolutegravir/rilpivirine combination product at least 4 hours before or 6 hours after oral magnesium salts. Risk D: Consider therapy modification

Doxercalciferol: May enhance the hypermagnesemic effect of Magnesium Salts. Management: Consider using a non-magnesium-containing antacid or phosphate-binding product in patients also receiving doxercalciferol. If magnesium-containing products must be used with doxercalciferol, serum magnesium concentrations should be monitored closely. Risk D: Consider therapy modification

Eltrombopag: Polyvalent Cation Containing Products may decrease the serum concentration of Eltrombopag. Management: Administer eltrombopag at least 2 hours before or 4 hours after oral administration of any polyvalent cation containing product. Risk D: Consider therapy modification

Elvitegravir: Polyvalent Cation Containing Products may decrease the serum concentration of Elvitegravir. Management: Administer elvitegravir 2 hours before or 6 hours after the administration of polyvalent cation containing products. Risk D: Consider therapy modification

Gabapentin: Magnesium Salts may enhance the CNS depressant effect of Gabapentin. Specifically, high dose intravenous/epidural magnesium sulfate may enhance the CNS depressant effects of gabapentin. Magnesium Salts may decrease the serum concentration of Gabapentin. Management: Administer gabapentin at least 2 hours after use of a magnesium-containing antacid. Monitor patients closely for evidence of reduced response to gabapentin therapy. Monitor for CNS depression if high dose IV/epidural magnesium sulfate is used. Risk D: Consider therapy modification

Levothyroxine: Magnesium Salts may decrease the serum concentration of Levothyroxine. Management: Separate administration of oral levothyroxine and oral magnesium salts by at least 4 hours. Risk D: Consider therapy modification

Multivitamins/Fluoride (with ADE): Magnesium Salts may decrease the serum concentration of Multivitamins/Fluoride (with ADE). Specifically, magnesium salts may decrease fluoride absorption. Management: To avoid this potential interaction separate the administration of magnesium salts from administration of a fluoride-containing product by at least 1 hour. Risk D: Consider therapy modification

Neuromuscular-Blocking Agents: Magnesium Salts may enhance the neuromuscular-blocking effect of Neuromuscular-Blocking Agents. Risk C: Monitor therapy

PenicillAMINE: Polyvalent Cation Containing Products may decrease the serum concentration of PenicillAMINE. Management: Separate the administration of penicillamine and oral polyvalent cation containing products by at least 1 hour. Risk D: Consider therapy modification

Phosphate Supplements: Magnesium Salts may decrease the serum concentration of Phosphate Supplements. Management: Administer oral phosphate supplements as far apart from the administration of an oral magnesium salt as possible to minimize the significance of this interaction. Risk D: Consider therapy modification

Quinolones: Magnesium Salts may decrease the serum concentration of Quinolones. Management: Administer oral quinolones several hours before (4 h for moxi/pe/spar/enox-, 2 h for others) or after (8 h for moxi-, 6 h for cipro/dela-, 4 h for lome/pe/enox-, 3 h for gemi-, and 2 h for levo-, nor-, or ofloxacin or nalidixic acid) oral magnesium salts. Risk D: Consider therapy modification

Raltegravir: Magnesium Salts may decrease the serum concentration of Raltegravir. Management: Avoid the use of oral / enteral magnesium salts with raltegravir. No dose separation schedule has been established that adequately reduces the magnitude of interaction. Risk X: Avoid combination

Roxadustat: Polyvalent Cation Containing Products may decrease the serum concentration of Roxadustat. Management: Administer roxadustat at least 1 hour after the administration of oral polyvalent cation containing products. Risk D: Consider therapy modification

Sodium Polystyrene Sulfonate: Laxatives (Magnesium Containing) may enhance the adverse/toxic effect of Sodium Polystyrene Sulfonate. More specifically, concomitant use of sodium polystyrene sulfonate with magnesium-containing laxatives may result in metabolic alkalosis or with sorbitol may result in intestinal necrosis. Management: Avoid concomitant use of sodium polystyrene sulfonate (rectal or oral) and magnesium-containing laxatives. Risk X: Avoid combination

Tetracyclines: Magnesium Salts may decrease the absorption of Tetracyclines. Only applicable to oral preparations of each agent. Management: Avoid coadministration of oral magnesium salts and oral tetracyclines. If coadministration cannot be avoided, administer oral magnesium at least 2 hours before, or 4 hours after, oral tetracyclines. Monitor for decreased tetracycline therapeutic effects. Risk D: Consider therapy modification

Trientine: Polyvalent Cation Containing Products may decrease the serum concentration of Trientine. Management: Avoid concomitant use of trientine and polyvalent cations. If oral iron supplements are required, separate the administration by 2 hours. For other oral polyvalent cations, give trientine 1 hour before, or 1 to 2 hours after the polyvalent cation. Risk D: Consider therapy modification

Unithiol: May diminish the therapeutic effect of Polyvalent Cation Containing Products. Risk X: Avoid combination

Pregnancy Considerations

Magnesium crosses the placenta; serum concentrations in the fetus are similar to those in the mother (Idama 1998; Osada 2002)

Breastfeeding Considerations

Magnesium is found in breast milk; concentrations remain constant during the first year of lactation and are not influenced by dietary intake under normal conditions. Magnesium requirements are the same in lactating and nonlactating females (IOM,1997).

Dietary Considerations

Should be taken with food and at least 8 oz of water. Whole grains, legumes, and dark-green leafy vegetables are dietary sources of magnesium.

Dietary reference intake (elemental magnesium) (IOM 1997):

1 to 6 months: Adequate intake: 30 mg/day.

7 to 12 months: Adequate intake: 75 mg/day.

1 to 3 years: Recommended dietary allowance (RDA): 80 mg/day.

4 to 8 years: RDA: 130 mg/day.

9 to 13 years: RDA: 240 mg/day.

14 to 18 years: RDA:

Females: 360 mg/day.

Pregnancy: 400 mg/day.

Lactation: 360 mg/day.

Males: 410 mg/day.

19 to 30 years: RDA:

Females: 310 mg/day.

Pregnancy: 350 mg/day.

Lactation: 310 mg/day.

Males: 400 mg/day.

≥31 years: RDA:

Females: 320 mg/day.

Pregnancy: 360 mg/day.

Lactation: 320 mg/day.

Males: 420 mg/day.

Reference Range

Serum magnesium: 1.5-2.5 mg/dL; slightly different ranges are reported by different laboratories

Mechanism of Action

Magnesium is important as a cofactor in many enzymatic reactions in the body involving protein synthesis and carbohydrate metabolism (at least 300 enzymatic reactions require magnesium). Actions on lipoprotein lipase have been found to be important in reducing serum cholesterol and on sodium/potassium ATPase in promoting polarization (eg, neuromuscular functioning).

Pharmacokinetics

Absorption: Oral: Up to 30%

Excretion: Urine (IOM 1997); feces (as unabsorbed drug)

Pricing: US

Tablets (Mag-200 Oral)

200 mg (per each): $0.07

Tablets (Mag-Oxide Oral)

200 mg (per each): $0.03

Tablets (Magnesium Oxide Oral)

400 mg (per each): $0.03 - $0.33

400 (240 Mg) mg (per each): $0.03 - $0.08

420 mg (per each): $0.04

420 (252 Mg) mg (per each): $0.06

500 mg (per each): $0.03

Tablets (MAGnesium-Oxide Oral)

400 (240 Mg) mg (per each): $0.15

Tablets (Maox Oral)

420 mg (per each): $0.04

Disclaimer: A representative AWP (Average Wholesale Price) price or price range is provided as reference price only. A range is provided when more than one manufacturer's AWP price is available and uses the low and high price reported by the manufacturers to determine the range. The pricing data should be used for benchmarking purposes only, and as such should not be used alone to set or adjudicate any prices for reimbursement or purchasing functions or considered to be an exact price for a single product and/or manufacturer. Medi-Span expressly disclaims all warranties of any kind or nature, whether express or implied, and assumes no liability with respect to accuracy of price or price range data published in its solutions. In no event shall Medi-Span be liable for special, indirect, incidental, or consequential damages arising from use of price or price range data. Pricing data is updated monthly.

Brand Names: International
  • Magnez (PL);
  • MAGO (KR);
  • Mayjou (TW);
  • Oximag (PL);
  • Plusssz Magnez (PL)


For country code abbreviations (show table)
  1. Anderson S, Farrington E. Magnesium treatment in pediatric patients. J Pediatr Health Care. 2021;35(5):564-571. doi:10.1016/j.pedhc.2021.03.003 [PubMed 34479684]
  2. Gal P, Reed M. Medications. In: Kliegman RM, Behrman RE, Jenson HB, et al, eds. Nelson Textbook of Pediatrics. 18th ed. Philadelphia, PA: Saunders Elsevier; 2007: 2955-2999.
  3. Idama TO and Lindow SW, "Magnesium Sulphate: A Review of Clinical Pharmacology Applied to Obstetrics," Br J Obstet Gynaecol, 1998, 105(3):260-8. [PubMed 9532984]
  4. IOM (Institute of Medicine), Dietary Reference Intakes for Calcium, Phosphorus, Magnesium, Vitamin D, and Fluoride, National Academy of Sciences, Washington, DC, 1997.
  5. Lo SF. Reference intervals for laboratory tests and procedures. In: Kliegman RM, St. Geme J, eds. Nelson Textbook of Pediatrics. 21st ed. Elsevier; 2020:chap 748.
  6. Magnesium oxide 250 mg tablet [prescribing information]. Ronkonkoma, NY: Sundance Vitamins, LLC; received January 2018.
  7. Magnesium oxide 400 mg tablet [prescribing information]. Deer Park, NY: Allegiant Health; January 2019.
  8. Magnesium oxide 420 mg tablet [prescribing information]. Deer Park, NY: Allegiant Health; November 2021.
  9. Osada H, Watanabe Y, Nishimura Y, et al, "Profile of Trace Element Concentrations in the Feto-Placental Unit in Relation to Fetal Growth," Acta Obstet Gynecol Scand, 2002, 81(10):931-7. [PubMed 12366483]
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