50% Magnesium Sulfate

The dosage of Magnesium Sulfate Heptahydrate must be strictly individualized based on the patient's clinical condition, serum magnesium levels, and renal function.

• For Eclampsia/Pre-eclampsia: A common regimen involves an initial loading dose of 4 to 5 grams IV (diluted) administered over 20 to 30 minutes, followed by a maintenance infusion of 1 to 2 grams per hour. Alternatively, 10 grams may be given intramuscularly (5g in each buttock) followed by 5g every 4 hours.
• For Severe Hypomagnesemia: 1 to 5 grams may be administered IM or IV in divided doses, with the rate not exceeding 1.5 mL of a 10% solution per minute.
• For Constipation (Oral): 10 to 30 grams of granules dissolved in 8 ounces of water. This is typically taken as a single dose or in divided doses over the course of a day.

Pediatric use must be managed with extreme caution by a specialist.

• Hypomagnesemia: 25 to 50 mg/kg per dose administered IV or IM every 4 to 6 hours for 3 to 4 doses.
• Constipation (Ages 6-12): 5 to 10 grams dissolved in water daily.
• Constipation (Ages 12+ ): Same as adult dosing (10 to 30 grams).
• Note: Magnesium sulfate is generally not recommended for children under 6 years of age as a laxative without direct medical supervision.

Renal Impairment

Patients with a GFR less than 30 mL/min require significant dose reductions, often by 50% or more. Serum magnesium levels must be monitored every 2 to 4 hours during IV therapy in these patients to prevent life-threatening toxicity.

Hepatic Impairment

No specific dosage adjustment is typically required for patients with liver disease, as the drug is cleared renally. However, patients with hepatorenal syndrome (liver failure causing kidney failure) must be treated as having renal impairment.

Elderly Patients

Older adults are at a higher risk of reduced renal clearance. Dosing should start at the lower end of the range, and frequent monitoring of kidney function and deep tendon reflexes is mandatory.

• IV/IM Administration: This must be performed by a healthcare professional in a clinical setting. IV doses must be diluted to a concentration of 20% or less before administration to prevent cardiac arrest.
• Oral Use: Dissolve the prescribed amount of granules in a full glass (8 oz) of water. You may add lemon juice to improve the bitter taste. Drink the entire mixture immediately.
• Timing: For laxative use, it is best taken on an empty stomach for faster results, which typically occur within 30 minutes to 6 hours.
• Storage: Store oral granules at room temperature (20°C to 25°C) in a dry place. Keep the container tightly closed.

If you are using this medication on a schedule and miss a dose, take it as soon as you remember. If it is almost time for your next dose, skip the missed dose and resume your regular schedule. Do not double the dose to catch up. For hospitalized patients receiving IV therapy, the infusion is continuous, and "missed doses" are managed by clinical staff.

Signs of magnesium overdose (hypermagnesemia) include:

• Loss of deep tendon reflexes (the most reliable early sign)
• Extreme drowsiness or lethargy
• Slurred speech
• Double vision
• Respiratory depression (slowed breathing)
• Cardiac arrest

Emergency Measure: In the event of a symptomatic overdose, the immediate administration of Calcium Gluconate (1 gram IV) is the standard antidote to antagonize the effects of magnesium. Hemodialysis may be required in severe cases.

> Important: Follow your healthcare provider's dosing instructions precisely. Do not adjust your dose or stop treatment without medical guidance, especially when being treated for serious conditions like pre-eclampsia.

When administered intravenously, especially at high doses for eclampsia, most patients will experience some degree of side effects. These are often related to the vasodilatory (widening of blood vessels) effects of magnesium:

• Flushing and Warmth: A sudden feeling of heat throughout the body, often accompanied by redness in the face and neck. This usually subsides shortly after the infusion rate is stabilized.
• Increased Sweating (Diaphoresis): Patients may feel clammy or damp.
• Thirst: A dry mouth or intense desire for water.
• Injection Site Reaction: Pain, redness, or swelling at the site of the IV or IM injection.

• Hypotension (Low Blood Pressure): This can cause lightheadedness or dizziness upon standing.
• Nausea and Vomiting: Often associated with the rapid administration of the loading dose.
• Headache: A dull or throbbing sensation.
• Muscle Weakness: A general feeling of heaviness in the limbs.
• Diarrhea: This is the intended effect when used as a laxative but may be an unwanted side effect when used for other indications.

• Hypocalcemia: Magnesium can suppress parathyroid hormone, leading to low calcium levels in the blood, which may cause muscle cramps or tingling in the extremities.
• Visual Disturbances: Blurred or double vision (diplopia).
• Confusion: Disorientation or difficulty concentrating.

> Warning: Stop taking Magnesium Sulfate Heptahydrate and call your doctor immediately if you experience any of these serious symptoms. These are often signs of magnesium toxicity.

• Loss of Deep Tendon Reflexes: If your doctor taps your knee and there is no "kick" response, this is a critical warning sign that magnesium levels are too high.
• Respiratory Paralysis: Difficulty breathing, shortness of breath, or a very slow breathing rate (less than 12 breaths per minute).
• Cardiac Arrhythmias: Feeling like your heart is skipping a beat, racing, or beating too slowly.
• Extreme Hypotension: Fainting or feeling like you are about to pass out.
• Decreased Urine Output (Oliguria): Since magnesium is cleared by the kidneys, a drop in urine production can lead to a rapid, dangerous buildup of the drug in the blood.
• Profound Lethargy: Inability to stay awake or respond to verbal commands.

Magnesium Sulfate Heptahydrate is generally intended for short-term use. Prolonged use (especially beyond 5 to 7 days in pregnant women) has been associated with:

• Fetal Bone Abnormalities: Prolonged in utero exposure can lead to low calcium levels and bone demineralization (thinning) in the newborn.
• Electrolyte Imbalance: Chronic use as a laxative can lead to dependency and significant imbalances in potassium, sodium, and calcium, potentially affecting heart and kidney function.
• Magnesium Accumulation: In patients with undiagnosed mild renal impairment, long-term use can lead to chronic hypermagnesemia, manifesting as persistent fatigue and muscle weakness.

There is currently no FDA black box warning for Magnesium Sulfate Heptahydrate. However, the FDA has issued a Drug Safety Communication warning against the prolonged use (more than 5-7 days) of magnesium sulfate injection for the treatment of preterm labor, as it can lead to low calcium levels and bone problems in the developing fetus.

Report any unusual symptoms to your healthcare provider immediately. Monitoring of serum magnesium levels is the standard of care during high-dose therapy to ensure safety.

Magnesium Sulfate Heptahydrate is a potent medication that requires careful clinical monitoring. It should only be used under the supervision of a healthcare professional who can monitor vital signs and electrolyte levels. The most critical safety concern is the narrow therapeutic index, meaning the difference between a therapeutic dose and a toxic dose can be small, especially in patients with underlying health conditions.

No FDA black box warnings for Magnesium Sulfate Heptahydrate. However, clinicians must adhere to the FDA safety alert regarding the duration of use in pregnancy (not to exceed 5-7 days for tocolysis).

• Allergic Reactions / Anaphylaxis: While rare, hypersensitivity reactions can occur. Symptoms include rash, itching, swelling of the face/tongue, and severe dizziness. Immediate medical intervention is required.
• Renal Insufficiency: This is the most significant risk factor for magnesium toxicity. If the kidneys cannot excrete magnesium efficiently, levels will rise to toxic peaks rapidly. Urine output must be monitored and should remain above 100 mL every 4 hours during IV therapy.
• Neuromuscular Diseases: Patients with conditions like Myasthenia Gravis or Lambert-Eaton syndrome are at extreme risk. Magnesium can exacerbate muscle weakness and precipitate a respiratory crisis by further inhibiting neuromuscular transmission.
• Cardiac Conditions: Magnesium affects cardiac conduction. It should be used with extreme caution in patients with heart block or known myocardial damage, as it can worsen these conditions or lead to cardiac arrest.

During intravenous administration of Magnesium Sulfate Heptahydrate, the following must be monitored at regular intervals (often every 1 to 4 hours):

1. 1Deep Tendon Reflexes (DTRs): Patellar reflexes must be present.
2. 2Respiratory Rate: Must be at least 12 to 16 breaths per minute.
3. 3Urine Output: Must be maintained at a minimum of 25-30 mL per hour.
4. 4Serum Magnesium Levels: The therapeutic range for seizure prevention is typically 4 to 7 mEq/L (4.8 to 8.4 mg/dL).
5. 5Fetal Heart Rate: Continuous monitoring is required when used in pregnant patients.

Magnesium sulfate can cause significant drowsiness, blurred vision, and muscle weakness. Patients receiving this medication should not drive or operate heavy machinery until the effects have completely worn off and they have been cleared by a physician.

Alcohol should be avoided while using magnesium sulfate, particularly when used as an oral laxative. Alcohol can exacerbate the dehydrating effects of the laxative and increase the risk of central nervous system depression, leading to extreme dizziness or confusion.

For oral laxative use, the drug should be discontinued if no bowel movement occurs after use, as this may indicate a more serious underlying condition like a bowel obstruction. For IV use in eclampsia, the medication is typically continued for 24 hours after delivery or 24 hours after the last seizure, then tapered or stopped as per clinical protocol.

> Important: Discuss all your medical conditions, especially kidney disease and neuromuscular disorders, with your healthcare provider before starting Magnesium Sulfate Heptahydrate.

• Nifedipine and other Calcium Channel Blockers (CCBs): While not strictly contraindicated in all settings, the combination of IV magnesium and CCBs (like nifedipine) can lead to an exaggerated hypotensive response and profound muscle weakness. The interaction is pharmacodynamic; both drugs inhibit calcium entry into cells, leading to synergistic effects on vascular smooth muscle and neuromuscular junctions.
• Neuromuscular Blocking Agents: Drugs such as vecuronium, rocuronium, or succinylcholine used during surgery must be used with extreme caution. Magnesium potentiates the effect of these blockers, potentially leading to prolonged respiratory paralysis after surgery.

• Aminoglycoside Antibiotics: Drugs like gentamicin or amikacin have their own neuromuscular blocking potential. When used with magnesium sulfate, the risk of respiratory failure increases significantly.
• Digitalis Glycosides (Digoxin): Magnesium can cause changes in cardiac conduction that may lead to heart block in patients taking digoxin. Conversely, if magnesium levels are too low, digoxin toxicity is more likely. Careful monitoring of the EKG is required.
• CNS Depressants: Opioids, benzodiazepines, and barbiturates can have additive sedative effects when used with magnesium, increasing the risk of profound lethargy and respiratory depression.

• Tetracycline and Quinolone Antibiotics: Oral magnesium can chelate (bind) to these antibiotics (e.g., doxycycline, ciprofloxacin) in the gut, significantly reducing their absorption and efficacy. These medications should be taken at least 2 hours before or 6 hours after oral magnesium sulfate.
• Bisphosphonates: Oral magnesium can interfere with the absorption of bone-strengthening medications like alendronate. Space doses by at least 2 hours.
• Potassium-Sparing Diuretics: Using magnesium with drugs like spironolactone can lead to increased magnesium levels, as these diuretics may reduce magnesium excretion.

• High-Fat Meals: May slightly delay the transit time of oral magnesium but do not significantly impact the total amount absorbed.
• Dairy Products: High calcium intake from dairy can compete with magnesium for absorption in the intestines. While not usually clinically significant for a single laxative dose, it can matter for long-term supplementation.

• St. John's Wort: May increase the risk of sedation when combined with the CNS-dampening effects of magnesium.
• Calcium Supplements: High doses of oral calcium can reduce the effectiveness of oral magnesium by competing for the same uptake transporters in the small intestine.

• Serum Calcium: Magnesium sulfate may cause a false decrease in serum calcium measurements depending on the laboratory method used.
• Serum Creatinine: High levels of magnesium can interfere with certain colorimetric assays for creatinine, potentially leading to inaccurate assessments of kidney function.

For each major interaction, the management strategy usually involves either spacing the doses, reducing the dosage of the interacting agent, or increasing the frequency of clinical monitoring (e.g., checking reflexes and respiratory rate more often).

> Important: Tell your doctor about ALL medications, supplements, and herbal products you are taking, including over-the-counter antacids and laxatives.

Magnesium Sulfate Heptahydrate must NEVER be used in the following conditions:

• Heart Block: Specifically high-grade SA or AV block. Magnesium slows cardiac conduction and can precipitate complete heart block or cardiac arrest in these patients.
• Myocardial Damage: In the setting of a recent acute myocardial infarction (heart attack) with significant tissue damage, magnesium may further destabilize cardiac rhythm.
• Myasthenia Gravis: This autoimmune neuromuscular disease is characterized by muscle weakness. Magnesium's ability to inhibit acetylcholine release can cause a "myasthenic crisis," leading to fatal respiratory failure.
• Severe Renal Failure: If the GFR is extremely low (e.g., <15 mL/min), the risk of rapid, uncontrollable magnesium toxicity is too high for standard use unless under extreme emergency conditions with dialysis available.

Conditions requiring a careful risk-benefit analysis include:

• Moderate Renal Impairment: Requires strict dose reduction and frequent lab monitoring.
• Digitalis Toxicity: Magnesium can worsen heart block associated with digitalis, though it is ironically used to treat certain digitalis-induced arrhythmias (like Torsades).
• Hypocalcemia: Because magnesium can further lower calcium levels, existing deficiency must be addressed cautiously.
• Dehydration: When used as a laxative, magnesium sulfate can worsen dehydration and electrolyte depletion.

There is no known cross-sensitivity between Magnesium Sulfate Heptahydrate and other classes of drugs. However, patients who have had a previous hypersensitivity reaction to any magnesium salt (such as magnesium citrate or magnesium oxide) should avoid magnesium sulfate heptahydrate.

> Important: Your healthcare provider will evaluate your complete medical history, including any history of heart disease or kidney problems, before prescribing Magnesium Sulfate Heptahydrate.

Magnesium Sulfate Heptahydrate is widely used in pregnancy for the management of eclampsia.

• FDA Pregnancy Category: It was traditionally Category D.
• Risks: While it is the treatment of choice for preventing eclamptic seizures, the FDA warns against its use for more than 5-7 days to stop preterm labor. Prolonged use can cause the fetus to develop low calcium levels and bone thinning (osteopenia).
• Benefits: In the context of eclampsia, the life-saving benefits for both mother and baby far outweigh the risks of short-term exposure.

Magnesium sulfate is excreted into breast milk. However, when used at standard doses, it is generally considered compatible with breastfeeding by the American Academy of Pediatrics. Oral absorption of magnesium by the infant is low, and the amount in milk is unlikely to cause adverse effects. Monitoring the infant for drowsiness or poor feeding is recommended if the mother is receiving high-dose IV therapy.

• Approved Indications: Used for hypomagnesemia and as a laxative in children over 6. It is also used in the treatment of acute nephritis with hypertension.
• Safety: Children are more susceptible to electrolyte imbalances and dehydration when using osmotic laxatives. Dosing must be strictly weight-based.
• Growth Effects: No long-term effects on growth have been documented with short-term use.

• Renal Risk: The elderly are at significantly higher risk for magnesium toxicity due to the natural age-related decline in GFR.
• Fall Risk: The muscle-relaxant and sedative effects of magnesium increase the risk of falls and fractures in older adults.
• Polypharmacy: Older patients are more likely to be on interacting medications like digoxin or diuretics, necessitating closer monitoring.

• Dose Adjustment: Mandatory for any patient with a creatinine clearance below 60 mL/min.
• Monitoring: Serum magnesium levels should be checked every 2-4 hours. The infusion should be stopped if the serum level exceeds the therapeutic range or if reflexes disappear.

No specific dose adjustments are needed for isolated liver disease, but clinicians must be alert for secondary renal issues (hepatorenal syndrome) that would impair magnesium clearance.

> Important: Special populations require individualized medical assessment and often more frequent laboratory monitoring to ensure safety.

Magnesium Sulfate Heptahydrate acts as a multifaceted pharmacological agent. Its primary molecular mechanism involves the competitive inhibition of calcium ions. By competing with calcium for binding sites on voltage-gated calcium channels, it reduces calcium influx into cells. In the nervous system, it acts as a voltage-dependent blocker of NMDA receptors, which prevents the excessive neuronal firing associated with seizures. In the peripheral nervous system, it reduces the amount of acetylcholine released from motor nerve terminals, exerting a muscle-relaxant effect.

• Onset of Action: For IV administration, the anticonvulsant effect is immediate. For IM administration, onset occurs within 60 minutes. As an oral laxative, effects are seen within 0.5 to 6 hours.
• Duration of Effect: IV effects last approximately 30 minutes after the infusion is stopped. IM effects last 3 to 4 hours.
• Therapeutic Range: 4 to 7 mEq/L for seizure prophylaxis.

| Parameter | Value |

|---|---|

| Bioavailability | 100% (IV); 30-40% (Oral) |

| Protein Binding | ~40% (to Albumin) |

| Half-life | 4-6 hours (Normal Renal Function) |

| Tmax | Immediate (IV); 1-2 hours (IM) |

| Metabolism | None (Inorganic Salt) |

| Excretion | Renal (>90% of absorbed dose) |

• Molecular Formula: MgSO4·7H2O
• Molecular Weight: 246.47 g/mol
• Solubility: Highly soluble in water (approx. 710 g/L at 20°C); slightly soluble in alcohol.
• Structure: It consists of a magnesium cation (Mg2+) and a sulfate anion (SO4 2-) associated with seven molecules of water of crystallization. It appears as small, colorless, needle-like crystals.

Magnesium Sulfate Heptahydrate is classified as an electrolyte replenisher, an anticonvulsant, and an osmotic laxative. In the context of the EPC system, it is also listed under Non-Standardized Food Allergenic Extracts and Lipid Emulsions when used as a component in those specialized medical products.