Product image of Magnokal (Potassium Hydrogen Aspartate Hemihydrate, Magnesium Aspartate Tetrahydrate) supplied by GNH India

Magnokal

Active Ingredient:
Potassium Hydrogen Aspartate Hemihydrate, Magnesium Aspartate Tetrahydrate
Origin:
EU

Magnokal (Potassium Hydrogen Aspartate Hemihydrate, Magnesium Aspartate Tetrahydrate)

Potassium hydrogen aspartate, the active ingredient in Magnokal, is a electrolyte supplement presented as an oral tablet for oral use. It helps correct potassium and magnesium deficiencies and supports electrolyte balance in adults.

GNH India supplies Magnokal as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Us Pharmacia Sp. Z O.O.

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Indications & Clinical Uses

Magnokal is used to address electrolyte disturbances and related conditions.

  • Potassium deficiency: helps restore normal potassium levels.
  • Magnesium deficiency: contributes to re‑establishing adequate magnesium status.
  • Electrolyte imbalance: supports overall electrolyte homeostasis.
  • Muscle cramps: may reduce the frequency and intensity of cramp episodes.

How It Works

  • Magnokal provides potassium and magnesium ions that are absorbed in the gastrointestinal tract and enter the extracellular fluid. The supplied ions participate in cellular processes such as nerve impulse transmission, muscle contraction, and enzymatic reactions, thereby helping to maintain normal electrolyte balance and supporting physiological functions that depend on adequate potassium and magnesium levels.

Side Effects

Adverse reactions may occur with oral electrolyte supplements.

Common Side Effects

  • Nausea: mild stomach upset after ingestion.
  • Abdominal discomfort: transient cramping or fullness.
  • Diarrhea: loose stools in some individuals.
  • Headache: occasional mild headache.

Serious or Rare Side Effects

  • Hyperkalemia: elevated blood potassium that can affect heart rhythm.
  • Hypermagnesemia: excess magnesium leading to muscle weakness or cardiac effects.
  • Severe allergic reaction: rash, swelling, or anaphylaxis.
  • Cardiac arrhythmia: irregular heartbeat in susceptible patients.
  • Respiratory depression: rare but serious breathing difficulty.

Precautions & Warnings

When using Magnokal, consider the following safety measures.

  • Renal impairment: monitor potassium and magnesium levels closely.
  • Cardiac disease: use with caution due to electrolyte effects on heart rhythm.
  • Concurrent diuretics: assess electrolyte status regularly.
  • Pregnancy and breastfeeding: safety not established; consult a healthcare professional.
  • Drug interactions: review all concomitant medications.
  • Store at ambient temperature below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Magnokal may interact with other medicines that affect electrolyte balance.

Major Interactions (Avoid)

  • ACE inhibitors: increased risk of hyperkalemia.
  • Potassium‑sparing diuretics: may cause excessive potassium accumulation.

Moderate Interactions (Monitor Closely)

  • Loop diuretics: may alter magnesium levels.
  • Digoxin: electrolyte shifts can affect drug toxicity.
  • Certain antibiotics (e.g., aminoglycosides): renal function changes may modify electrolyte handling.

Frequently Asked Questions

Magnokal is an oral electrolyte supplement that provides potassium and magnesium ions. It is used to correct potassium and magnesium deficiencies, support overall electrolyte balance, and help alleviate symptoms such as muscle cramps that arise from electrolyte disturbances.

Potassium hydrogen aspartate dissociates in the gastrointestinal tract, releasing potassium ions that are absorbed into the bloodstream. The potassium contributes to cellular functions like nerve impulse transmission and muscle contraction, helping to restore normal potassium levels and maintain electrolyte homeostasis.

The appropriate dose of Magnokal is determined by the prescribing healthcare professional based on the individual’s electrolyte status, age, renal function, and other clinical factors. Patients should follow the specific instructions provided by their prescriber and not adjust the dose on their own.

Safety data for Magnokal in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. Women who are pregnant, planning to become pregnant, or breastfeeding should discuss potential risks and benefits with their healthcare provider before using the supplement.

To order Magnokal, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, and will request trade or institutional credentials. The team then replies with pricing, availability, shipping details, and any necessary import documentation.

Magnokal combines potassium hydrogen aspartate and magnesium aspartate in a single oral formulation, offering both potassium and magnesium replenishment. Compared with single‑ion supplements, it provides a broader electrolyte correction, which can be advantageous for patients needing simultaneous potassium and magnesium support.

Magnokal should be stored at ambient temperature below 25 °C. Keep the product in its original packaging, protect it from moisture, and store it out of direct sunlight to maintain stability and potency throughout its shelf life.

Magnokal is taken orally, typically with a glass of water. The exact timing (e.g., with meals or on an empty stomach) should follow the prescribing clinician’s guidance, which may consider the patient’s overall medication regimen and gastrointestinal tolerance.

The most serious risks include hyperkalemia and hypermagnesemia, which can lead to cardiac arrhythmias, muscle weakness, or respiratory depression. Severe allergic reactions such as anaphylaxis are also possible, though rare. Patients should seek immediate medical attention if they experience symptoms like palpitations, severe weakness, or breathing difficulty.

Magnokal should be avoided in individuals with known hypersensitivity to any of its ingredients, severe renal impairment, uncontrolled cardiac arrhythmias, or those taking medications that significantly raise potassium or magnesium levels without close monitoring. Healthcare providers should evaluate each patient’s medical history before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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