Product image of Murexal (Suxamethonium Chloride Dihydrate) supplied by GNH India

Murexal

Active Ingredient:
Suxamethonium Chloride Dihydrate
Origin:
EU

Murexal (Suxamethonium Chloride Dihydrate)

Suxamethonium chloride, the active ingredient in Murexal, is a neuromuscular blocking agent presented as a sterile injectable solution for intravenous use. It provides rapid skeletal muscle relaxation to facilitate tracheal intubation and to support surgical procedures that require controlled ventilation. The drug acts within seconds, producing a brief depolarizing block of the neuromuscular junction.

GNH India supplies Murexal as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide. The company ensures quality compliance with EU standards and provides reliable global distribution to meet clinical demand.

Manufacturer / TM Owner

Laboratoire Aguettant

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Indications & Clinical Uses

Murexal (suxamethonium chloride) is used in clinical settings that require rapid depolarizing muscle relaxation.

  • Tracheal intubation: provides swift muscle relaxation to enable safe placement of an endotracheal tube.
  • Surgical procedures: facilitates controlled ventilation and muscle relaxation during operations that require neuromuscular blockade.
  • Emergency airway management: allows rapid sequence induction for urgent airway control in critical care situations.

How It Works

  • Suxamethonium chloride acts as an acetylcholine receptor agonist at the nicotinic sites of the motor end‑plate. It binds and activates these receptors, causing an initial depolarization and muscle fasciculation, followed by a sustained depolarized state that renders the end‑plate unresponsive to further stimulation, producing a temporary phase I neuromuscular block.

Side Effects

Suxamethonium chloride may be associated with a range of adverse reactions, which are categorized by frequency.

Common Side Effects

  • Transient hyperkalemia: mild increase in serum potassium levels that usually resolves spontaneously.
  • Flushing or erythema: temporary skin reddening at the injection site.
  • Muscle fasciculations: brief involuntary muscle twitches during onset.
  • Elevated intra‑ocular pressure: temporary rise in eye pressure.

Serious or Rare Side Effects

  • Malignant hyperthermia: life‑threatening hypermetabolic reaction triggered in susceptible individuals.
  • Prolonged apnea: extended respiratory paralysis requiring mechanical ventilation.
  • Cardiac arrhythmias: abnormal heart rhythms, especially in patients with electrolyte disturbances.
  • Anaphylaxis: severe allergic reaction that can be fatal if not treated promptly.

Precautions & Warnings

When using Murexal, clinicians should observe several safety measures.

  • Assess patient history: identify known susceptibility to malignant hyperthermia or hyperkalemia.
  • Monitor neuromuscular function: use peripheral nerve stimulator to gauge depth of block.
  • Avoid in hyperkalemic patients: elevated serum potassium can worsen cardiac risk.
  • Use cautiously in cardiac disease: monitor heart rate and blood pressure during administration.
  • Adjust for renal impairment: consider reduced clearance in severe renal dysfunction.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Potential drug interactions with suxamethonium chloride require careful evaluation.

Major Interactions (Avoid)

  • Concurrent use with non‑depolarizing neuromuscular blockers: may cause prolonged paralysis.
  • Combination with potassium‑increasing agents (e.g., potassium chloride): can exacerbate hyperkalemia.
  • Co‑administration with volatile anesthetics that trigger malignant hyperthermia: increases risk of hypermetabolic crisis.

Moderate Interactions (Monitor Closely)

  • Anticholinesterases (e.g., neostigmine): may alter duration of block and cause cholinergic side effects.
  • Magnesium sulfate: potentiates neuromuscular blockade and may require dose adjustment.
  • Beta‑adrenergic blockers: can modify cardiovascular responses during administration.

Frequently Asked Questions

Murexal contains suxamethonium chloride, a depolarizing neuromuscular blocking agent. It is employed by anesthesiologists to produce rapid skeletal muscle relaxation, primarily to facilitate tracheal intubation and to provide a controlled muscle‑relaxed state during surgical procedures that require mechanical ventilation.

Suxamethonium chloride mimics acetylcholine at the nicotinic receptors of the motor end‑plate. It binds and activates these receptors, causing an initial depolarization and muscle fasciculation, followed by a sustained depolarized state that renders the end‑plate unresponsive to further stimulation, resulting in a temporary phase I neuromuscular block.

The dose of Murexal is determined by the prescribing clinician based on the patient’s age, weight, clinical condition, and the required depth of muscle relaxation. The prescriber calculates the appropriate amount and administers it intravenously under continuous monitoring.

The safety of suxamethonium chloride in pregnancy and lactation has not been definitively established. It should only be used when the potential benefit justifies any possible risk to the fetus or infant, and the decision must be made by the treating physician.

To place an order, visit the product page on gnhindia.com, enter the required quantity, and submit the enquiry form. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed), and any required import documentation.

Unlike non‑depolarizing agents, suxamethonium chloride produces a rapid onset of action within seconds and a short duration of effect, making it ideal for rapid sequence induction. Non‑depolarizing blockers generally have a slower onset and longer duration, which may be preferable for prolonged surgical procedures.

Murexal should be stored at 2‑8 °C in a refrigerator. Keep the vial in its original packaging, protect it from light, and avoid freezing or shaking the solution to maintain stability and potency.

Murexal is supplied as a sterile injectable solution for intravenous use. It is administered as a bolus injection into a peripheral or central vein, usually after confirming the patient’s airway and monitoring equipment are ready, and the patient is observed for the onset of muscle relaxation.

The most critical adverse events include malignant hyperthermia, a potentially fatal hypermetabolic reaction; prolonged apnea requiring assisted ventilation; severe hyperkalemia that can precipitate cardiac arrhythmias; and anaphylactic shock. Immediate recognition and appropriate emergency management are essential.

Murexal is contraindicated in patients with known susceptibility to malignant hyperthermia, existing hyperkalemia, severe burns, extensive muscle trauma, or certain neuromuscular disorders such as muscular dystrophy. It should also be used with caution in patients with significant cardiac disease or renal impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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