Magnesium Salicylate - Uses, Dose, Side effects, MOA, Brands

Magnesium Salicylate is used for the treatment of patients with mild to moderate pain, fever, and inflammation as in patients with rheumatoid arthritis and osteoarthritis.

Magnesium salicylate Uses:

  • It is used in the treatment of mild-to-moderate pain, fever, and other inflammatory conditions.
  • It may be used for the relief of pain and inflammation in patients with rheumatoid arthritis and osteoarthritis.

Magnesium Dose in Adults:

Magnesium Dose in the treatment of Relief of mild-to-moderate pain:

  • Doan's® Extra Strength, Momentum®:

    • Two caplets every 6 hours as required.
    • The maximum dose is 8 caplets/24 hours.
  • Keygesic:

    • One tablet every 4 hours as required.
    • The maximum dose is 4 tablets per day.

Magnesium Dose in Childrens:

Magnesium salicylate dose in the treatment of Relief of mild-to-moderate pain:

  • Children ≥12 years:

    • Refer to adult dosing.

Pregnancy Category: C (D in the third trimester)

  • Refer to Aspirin monograph for additional information.

Use during breastfeeding:

  • Salicylates are excreted in human breastmilk.
  • Refer to the Aspirin monograph for additional information.

Dose in Kidney disease:

  • Use with caution in patients with mild to moderate kidney disease.
  • Avoid in severe and advanced renal impairment.

Dose in Liver disease:

  • Avoid in patients with advanced liver disease.
  • Use with caution in patients with mild to moderate hepatic dysfunction.

Side effects of Magnesium Salicylate:

Refer to Aspirin monograph.


Contraindications to Magnesium salicylate:

  • Hypersensitivity to magnesium salicylate, salticylates, and other NSAIDs or any component of formulation
  • Advanced chronic renal disease;
  • Concomitant use of uricosuric drugs
  • Patients 65 years old and older should consult:
    • Patients with chronic salicylate use history, chronic liver disease and carditis are also advised not to take it.

Warnings and precautions

  • Sensitivity to salicylates:

    • Tartrazine dyes, nasal polyps and asthma patients should be cautious when using the drug.
  • Tinnitus

    • Patients with tinnitus and impaired hearing should stop using the treatment.
  • Bleeding disorders:

    • It can cause platelet dysfunction, so patients with bleeding disorders should be cautious.
  • Dehydration

    • Patients suffering from dehydration should be cautious.
  • Use of ethanol:

    • Patients who consume more than 3 ethanol drinks per day should not use it. These patients are at high risk for bleeding.
  • Gastrointestinal Disease:

    • Patients with erosive gastritis and peptic ulcer disease should not use it.
  • Hepatic impairment

    • Patients with severe liver disease should use caution.
  • Hypoprothrombinemia, vitamin K deficiency

    • Patients with hypoprothrombinemia or vitamin k deficiency should not use it.
  • Renal impairment

    • Patients with severe kidney impairment should avoid it.

Magnesium salicylate: Drug Interaction

Risk Factor C (Monitor therapy)

Agents with Antiplatelet Properties (e.g., P2Y12 inhibitors, NSAIDs, SSRIs, etc.)

May enhance the adverse/toxic effect of Salicylates. Increased risk of bleeding may result.

Ajmaline

Salicylates may enhance the adverse/toxic effect of Ajmaline. Specifically, the risk for cholestasis may be increased.

Ammonium Chloride

May increase the serum concentration of Salicylates.

Angiotensin-Converting Enzyme Inhibitors

Salicylates may enhance the nephrotoxic effect of Angiotensin-Converting Enzyme Inhibitors. Salicylates may diminish the therapeutic effect of Angiotensin-Converting Enzyme Inhibitors.

Anticoagulants

Salicylates may enhance the anticoagulant effect of Anticoagulants.

Benzbromarone

Salicylates may diminish the therapeutic effect of Benzbromarone.

Blood Glucose Lowering Agents

Salicylates may enhance the hypoglycemic effect of Blood Glucose Lowering Agents.

Calcium Channel Blockers

May enhance the adverse/toxic effect of Magnesium Salts. Magnesium Salts may enhance the hypotensive effect of Calcium Channel Blockers.

Corticosteroids (Systemic)

Salicylates may enhance the adverse/toxic effect of Corticosteroids (Systemic). These specifically include gastrointestinal ulceration and bleeding. Corticosteroids (Systemic) may decrease the serum concentration of Salicylates. Withdrawal of corticosteroids may result in salicylate toxicity.

Loop Diuretics

Salicylates may diminish the diuretic effect of Loop Diuretics. Loop Diuretics may increase the serum concentration of Salicylates.

Neuromuscular-Blocking Agents

Magnesium Salts may enhance the neuromuscular-blocking effect of Neuromuscular-Blocking Agents.

Probenecid

Salicylates may diminish the therapeutic effect of Probenecid.

Salicylates

May enhance the anticoagulant effect of other Salicylates.

Thrombolytic Agents

Salicylates may enhance the adverse/toxic effect of Thrombolytic Agents. An increased risk of bleeding may occur.

Valproate Products

Salicylates may increase the serum concentration of Valproate Products.

Risk Factor D (Consider therapy modification)

Alfacalcidol

May increase the serum concentration of Magnesium Salts.

Alpha-Lipoic Acid

Magnesium Salts may decrease the absorption of Alpha-Lipoic Acid. AlphaLipoic Acid may decrease the absorption of Magnesium Salts.

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.

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. Exceptions: Pamidronate; Zoledronic Acid.

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.

Carbonic Anhydrase Inhibitors

Salicylates may enhance the adverse/toxic effect of Carbonic Anhydrase Inhibitors. Salicylate toxicity might be enhanced by this same combination. Management: Avoid these combinations when possible.Dichlorphenamide use with high-dose aspirin as contraindicated. If another combination is used, monitor patients closely for adverse effects. Tachypnea, anorexia, lethargy, and coma have been reported. Exceptions: Brinzolamide; Dorzolamide.

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.

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.

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.

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.

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 magnesiumcontaining 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.

Ginkgo Biloba

May enhance the anticoagulant effect of Salicylates. Management: Consider alternatives to this combination of agents. Monitor for signs and symptoms of bleeding (especially intracranial bleeding) if salicylates are used in combination with ginkgo biloba.

Herbs (Anticoagulant/Antiplatelet Properties) (eg, Alfalfa, Anise, Bilberry)

May enhance the adverse/toxic effect of Salicylates. Bleeding may occur.

Hyaluronidase

Salicylates may diminish the therapeutic effect of Hyaluronidase. Management: Patients receiving salicylates (particularly at larger doses) may not experience the desired clinical response to standard doses of hyaluronidase. Larger doses of hyaluronidase may be required.

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.

Methotrexate

Salicylates may increase the serum concentration of Methotrexate. Salicylate doses used for prophylaxis of cardiovascular events are not likely to be of concern.

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.

Mycophenolate

Magnesium Salts may decrease the serum concentration of Mycophenolate. Management: Separate doses of mycophenolate and oral magnesium salts. Monitor for reduced effects of mycophenolate if taken concomitant with oral magnesium salts.

Nonsteroidal Anti-Inflammatory Agents (Nonselective)

May enhance the adverse/toxic effect of Salicylates. An increased risk of bleeding may be associated with use of this combination. Nonsteroidal Anti-Inflammatory Agents (Nonselective) may diminish the cardioprotective effect of Salicylates. Salicylates may decrease the serum concentration of Nonsteroidal Anti-Inflammatory Agents (Nonselective).

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.

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. Exceptions: Sodium Glycerophosphate Pentahydrate.

PRALAtrexate

Salicylates may increase the serum concentration of PRALAtrexate. Salicylate doses used for prophylaxis of cardiovascular events are unlikely to be of concern.

Quinolones

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

Tetracyclines

Magnesium Salts may decrease the absorption of Tetracyclines. Only applicable to oral preparations of each agent. Exceptions: Eravacycline.

Trientine

Polyvalent Cation Containing Products may decrease the serum concentration of Trientine. Management: Avoid concomitant administration of trientine and oral products that contain polyvalent cations. If oral iron supplements are required, separate the administration by 2 hours. If other oral polyvalent cations are needed, separate administration by 1 hour.

Vitamin K Antagonists (eg, warfarin)

Salicylates may enhance the anticoagulant effect of Vitamin K Antagonists.

Risk Factor X (Avoid combination)

Baloxavir Marboxil

Polyvalent Cation Containing Products may decrease the serum concentration of Baloxavir Marboxil.

Dexketoprofen

Salicylates may enhance the adverse/toxic effect of Dexketoprofen. Dexketoprofen may diminish the therapeutic effect of Salicylates. Salicylates may decrease the serum concentration of Dexketoprofen. Management: The use of high-dose salicylates (3 g/day or more in adults) together with dexketoprofen is inadvisable. Consider administering dexketoprofen 30-120 min after or at least 8 hrs before cardioprotective doses of aspirin to minimize any possible interaction.

Influenza Virus Vaccine (Live/Attenuated)

May enhance the adverse/toxic effect of Salicylates. Specifically, Reye's syndrome may develop.

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.

Sulfinpyrazone

Salicylates may decrease the serum concentration of Sulfinpyrazone.

Varicella Virus-Containing Vaccines

Salicylates may enhance the adverse/toxic effect of Varicella Virus-Containing Vaccines. Specifically, the risk for Reye's syndrome may increase.

 

Monitoring Parameters:

Monitor Renal functions in patients on long-term therapy and those with pre-existing renal impairment.


How to administer Magnesium salicylate?

Administer after meals with a full glass of water.


Mechanism of action of Magnesium salicylate:

  • It decreases inflammation, pain, fever, and by irreversibly inhibiting cyclooxygenase-1 (COX-1) enzymes via acetylation.
  • This results in decreased production of prostaglandin A precursors and thromboxane B precursors.

Absorption:

  • It is rapidly absorbed from the stomach and upper intestine.

Distribution:

  • It is distributed readily into tissues and most body fluids.

Protein binding:

  • 50% to 90% of the drug is bound to plasma proteins, primarily to albumin.

Metabolism:

  • It is released into the plasma as salicylic acid that is enzymatically converted to salicyluric acid and salicylphenolic glucuronide

Half-life elimination:

  • About 2 hours;
  • The half-life is increased with repeated dosing

Time to peak effect:

  • 1.5 hours

Excretion:

  • Urine

International Brand Names of Magnesium salicylate:

  • Doans Extra Strength
  • Doans Pills
  • Bexidermil
  • Dencorub
  • Geniol Flex
  • Metsal AR
  • Salimag
  • Topicrem

Magnesium salicylate Brand Names in Pakistan:

Magnesium Salicylate Tablets 250 mg in Pakistan

Femistar Max Drug Pharm (Pvt) Ltd.

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