|
| U.S. Brand
Names |
|
| Maox® |

|
|
| Generic
Available |
|
|
Yes |

|
|
| Pharmacological Index |
|
|
Antacid; Electrolyte Supplement, Oral; Laxative, Saline; Magnesium
Salt |

|
|
| Use |
|
|
Short-term treatment of occasional constipation and symptoms of
hyperacidity |

|
|
| Pregnancy Risk
Factor |
|
|
B |

|
|
| Contraindications |
|
|
Patients with colostomy or an ileostomy, appendicitis, ulcerative colitis,
diverticulitis, heart block, myocardial damage, serious renal impairment,
hepatitis, Addison's disease, hypersensitivity to any
component |

|
|
| Warnings/Precautions |
|
|
Hypermagnesemia and toxicity may occur due to decreased renal clearance
(Clcr <30 mL/minute) of absorbed magnesium; monitor serum
magnesium level, respiratory rate, deep tendon reflex, renal function when
MgSO4 is administered parenterally; use with caution in digitalized
patients (may alter cardiac conduction leading heart block); use with caution in
patients with lithium administration; elderly, due to disease or drug therapy,
may be predisposed to diarrhea; diarrhea may result in electrolyte imbalance;
monitor for toxicity |

|
|
| Adverse
Reactions |
|
|
>10%: Gastrointestinal: Diarrhea
1% to 10%:
Cardiovascular: Hypotension, EKG changes
Central nervous system: Mental depression, coma
Gastrointestinal: Nausea, vomiting
Respiratory: Respiratory depression |

|
|
| Overdosage/Toxicology |
|
|
Magnesium antacids are also laxative and may cause diarrhea and hypokalemia.
In patients with renal failure, magnesium may accumulate to toxic levels.
I.V. calcium (5-10 mEq) will reverse respiratory depression or heart block;
in extreme cases, peritoneal dialysis or hemodialysis may be required.
|

|
|
| Drug
Interactions |
|
|
Decreased effect: Tetracyclines, digoxin, indomethacin, iron salts,
isoniazid, quinolones |

|
|
| Mechanism of
Action |
|
|
Promotes bowel evacuation by causing osmotic retention of fluid which
distends the colon with increased peristaltic activity |

|
|
| Pharmacodynamics/Kinetics |
|
|
Onset of laxative action: 4-8 hours
Elimination: Absorbed magnesium ions (up to 30%) are usually excreted by
kidneys, unabsorbed drug is excreted in feces |

|
|
| Usual Dosage |
|
|
Adults: Oral:
Antacid: 140 mg 3-4 times/day or 400-840 mg/day
Laxative: 2-4 g at bedtime with full glass of water
Dosing in renal impairment: Patients in severe renal failure should
not receive magnesium due to toxicity from accumulation. Patients with a
Clcr <25 mL/minute should be monitored by serum magnesium levels.
Note: Oral magnesium is not generally adequate for repletion in
patients with serum magnesium concentrations <1.5 mEq/L |

|
|
| Dietary
Considerations |
|
|
Should be administered after meals |

|
|
| Administration |
|
|
Tablet may be chewed |

|
|
| Reference Range |
|
|
Serum magnesium:
Adults: 1.5-2.5 mg/dL (1.2-2.0 mEq/L) |

|
|
| Test
Interactions |
|
|
magnesium;
protein,
calcium (S), potassium
(S)
|

|
|
| Mental Health: Effects
on Mental Status |
|
|
May rarely cause depression |

|
|
| Mental Health:
Effects on Psychiatric
Treatment |
|
|
None reported |

|
|
| Dental Health: Local
Anesthetic/Vasoconstrictor
Precautions |
|
|
No information available to require special precautions |

|
|
| Dental Health:
Effects on Dental Treatment |
|
|
Magnesium products may prevent gastrointestinal absorption of tetracyclines
by forming a large ionized chelated molecule with the tetracyclines in the
stomach. Tetracyclines should be given at least 1 hour before
magnesium. |

|
|
| Patient
Information |
|
|
Chew tablets before swallowing; take with full glass of water; notify
physician if relief not obtained or if any signs of bleeding occur (black tarry
stools, "coffee ground" vomit) |

|
|
| Nursing
Implications |
|
|
Monitor for diarrhea and signs of hypermagnesemia |

|
|
| Dosage Forms |
|
|
Capsule: 140 mg
Tablet: 400 mg, 425 mg |

|
|
| References |
|
|
Chernow B, Smith J, Rainey TG, et al,
"Hypomagnesemia: Implications for the Critical Care Specialist," Crit Care
Med, 1982, 10(3):193-6.
Gams JG, "Clinical Significance of Magnesium: A Review," Drug Intell Clin
Pharm, 1987, 21(3):240-6. |

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