Product image of Mivuxin (Noradrenaline Tartrate) supplied by GNH India

Mivuxin

Active Ingredient:
Noradrenaline Tartrate
Origin:
EU

Mivuxin (Noradrenaline Tartrate)

Noradrenaline tartrate, the active ingredient in Mivuxin, is a sympathomimetic presented as an intravenous solution for intravenous use. It is employed to raise blood pressure in acute settings such as severe hypotension, septic shock, and cardiac arrest, acting directly on vascular smooth muscle to increase systemic vascular resistance.

GNH India supplies Mivuxin as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. The product complies with European Union regulatory standards and is distributed under strict quality‑assurance protocols.

Manufacturer / TM Owner

Laboratoire Aguettant

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Indications & Clinical Uses

Mivuxin is a vasopressor used in critical care to counteract profound circulatory failure.

  • Hypotension: restores arterial pressure by inducing peripheral vasoconstriction in patients with severe low blood pressure.
  • Septic shock: supports hemodynamics by increasing systemic vascular resistance when fluid resuscitation alone is insufficient.
  • Cardiac arrest: provides immediate pressor support during advanced cardiac life support to improve coronary and cerebral perfusion.

How It Works

  • Noradrenaline tartrate acts as a direct agonist at alpha‑1 adrenergic receptors on vascular smooth muscle, producing potent vasoconstriction and raising systemic vascular resistance. The resulting increase in arterial pressure improves organ perfusion in states of shock. At higher concentrations, it may also stimulate beta‑1 receptors, modestly enhancing cardiac contractility and heart rate.

Side Effects

Mivuxin may cause a range of adverse reactions that vary with dose, infusion rate, and patient condition.

Common Side Effects

  • Tachycardia: rapid heart rate due to beta‑1 stimulation.
  • Headache: secondary to elevated blood pressure.
  • Anxiety or restlessness: central nervous system response.
  • Peripheral ischemia: reduced blood flow to extremities.
  • Extravasation injury: tissue damage if the solution leaks from the vein.
  • Nausea: gastrointestinal upset.

Serious or Rare Side Effects

  • Myocardial ischemia: reduced coronary blood flow leading to chest pain.
  • Severe hypertension: excessive rise in blood pressure causing vascular injury.
  • Cardiac arrhythmias: potentially life‑threatening rhythm disturbances.
  • Tissue necrosis at infusion site: severe extravasation requiring surgical intervention.
  • Pulmonary edema: fluid accumulation in lungs due to increased afterload.
  • Limb gangrene: extreme peripheral vasoconstriction in susceptible patients.

Precautions & Warnings

When using Mivuxin, clinicians should observe several safety measures to minimize risk.

  • Dose titration: adjust the infusion rate to achieve target blood pressure while avoiding overshoot.
  • Cardiac monitoring: continuous ECG and hemodynamic monitoring are essential.
  • Peripheral perfusion: inspect limbs regularly for signs of ischemia or discoloration.
  • Extravasation risk: use central venous access when possible and have phentolamine readily available.
  • Pregnancy: consider use only if the potential benefit justifies the potential risk to the fetus.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Mivuxin can interact with several drug classes, influencing its efficacy or safety.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): may precipitate hypertensive crisis when combined.
  • Beta‑blockers: can blunt the desired increase in heart rate and cardiac output.
  • Tricyclic antidepressants: additive vasoconstrictive effects may raise blood pressure excessively.

Moderate Interactions (Monitor Closely)

  • Other vasopressors (e.g., dopamine, phenylephrine): additive pressor effects may require dose reduction.
  • Calcium channel blockers: may alter vascular tone and affect response.
  • Diuretics: changes in intravascular volume can modify pressor requirements.

Frequently Asked Questions

Mivuxin is an intravenous vasopressor indicated for the rapid correction of severe hypotension, management of septic shock, and provision of pressor support during cardiac arrest. It is used in intensive care and emergency settings where immediate elevation of arterial pressure is required to maintain organ perfusion.

Noradrenaline tartrate acts as a direct agonist at alpha‑1 adrenergic receptors on vascular smooth muscle, causing potent vasoconstriction and raising systemic vascular resistance. This increase in vascular tone elevates arterial pressure, while higher concentrations may also stimulate beta‑1 receptors, modestly enhancing heart rate and contractility.

The dosing regimen for Mivuxin is individualized. A qualified prescriber determines the initial infusion rate and subsequent titration based on the patient’s hemodynamic response, target blood pressure, and clinical condition. Continuous monitoring guides adjustments to achieve the desired therapeutic effect.

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

To order Mivuxin, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request verification of trade or institutional credentials. After confirmation, the team provides pricing, availability, shipping details (including cold‑chain logistics if needed) and assists with import documentation.

Mivuxin (noradrenaline) is often compared with dopamine or epinephrine. Noradrenaline provides stronger alpha‑mediated vasoconstriction with less tachycardia than dopamine, making it preferred for septic shock. Epinephrine has both alpha and beta activity but may cause more pronounced arrhythmias. Choice depends on the clinical scenario and physician judgment.

Mivuxin must be stored refrigerated at 2‑8 °C. It should be kept in its original container, protected from light, and must not be frozen or shaken. Prior to use, inspect the solution for particulate matter or discoloration and allow it to reach room temperature if required for infusion.

Mivuxin is administered intravenously, typically via a central venous catheter to reduce the risk of extravasation. The infusion is started at a low rate and titrated according to the patient’s blood pressure response, with continuous hemodynamic monitoring throughout the treatment period.

Serious risks include severe hypertension, myocardial ischemia, life‑threatening arrhythmias, and tissue necrosis at the infusion site due to extravasation. Clinicians should monitor blood pressure, cardiac rhythm, and peripheral perfusion closely, and be prepared to intervene promptly if any of these complications arise.

Mivuxin is contraindicated in patients with known hypersensitivity to noradrenaline or any excipients, uncontrolled hypertension, and severe peripheral vascular disease where further vasoconstriction could cause critical limb ischemia. Use in these populations should be avoided or undertaken only with extreme caution under specialist supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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