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

Mykronor

Active Ingredient:
Noradrenaline Tartrate
Origin:
EU

Mykronor (Noradrenaline Tartrate)

Noradrenaline tartrate, the active ingredient in Mykronor, is a sympathomimetic presented as an injectable solution for intravenous use. It acts as a potent vasopressor to raise blood pressure in patients experiencing severe hypotension, including those in septic or cardiogenic shock. The drug rapidly stimulates alpha‑adrenergic receptors, producing vasoconstriction and improving organ perfusion during critical care.

GNH India supplies Mykronor as a licensed, GDP‑compliant international pharmaceutical product to hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. Our distribution network ensures timely delivery and regulatory compliance across multiple regions.

Manufacturer / TM Owner

Laboratoire Aguettant

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Indications & Clinical Uses

Mykronor is used as a vasopressor in critical care settings to manage low blood pressure and shock states.

  • Hypotension: restores arterial pressure and improves tissue perfusion in patients with acute drops in blood pressure.
  • Septic shock: counteracts vasodilatory failure by increasing systemic vascular resistance, supporting hemodynamic stability.
  • Cardiogenic shock: augments preload and afterload to sustain cardiac output during severe heart failure.

How It Works

  • Noradrenaline tartrate acts as a direct agonist at alpha‑1 adrenergic receptors on vascular smooth muscle. Binding triggers intracellular calcium influx, leading to potent vasoconstriction and an increase in systemic vascular resistance. The resultant rise in arterial pressure helps maintain organ perfusion during states of profound hypotension. The drug’s rapid onset and short half‑life allow precise titration under continuous hemodynamic monitoring.

Side Effects

Noradrenaline tartrate may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Headache: mild to moderate headache occurring during infusion.
  • Tachycardia: increased heart rate as a reflex response to vasoconstriction.
  • Palpitations: sensation of irregular or forceful heartbeats.
  • Nausea: transient nausea reported in some patients.
  • Peripheral ischemia: reduced blood flow to extremities causing coldness or discoloration.

Serious or Rare Side Effects

  • Cardiac arrhythmias: potentially life‑threatening rhythm disturbances.
  • Myocardial ischemia: reduced coronary blood flow leading to chest pain.
  • Severe hypertension: abrupt, uncontrolled rise in blood pressure.
  • Tissue necrosis: local tissue death at extravasation sites.
  • Pulmonary edema: fluid accumulation in lungs due to increased afterload.

Precautions & Warnings

When using Mykronor, clinicians should observe specific precautions to minimize risks and ensure safe administration.

  • Dose titration: adjust infusion rate based on continuous blood pressure monitoring.
  • Cardiac monitoring: observe for arrhythmias and ischemic changes during therapy.
  • Extravasation risk: avoid infiltration; stop infusion immediately if leakage is suspected.
  • Fluid balance: assess volume status to prevent overload or depletion.
  • Concomitant vasopressors: evaluate cumulative pressor effect when combined with other agents.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Noradrenaline tartrate can interact with other medications, influencing its efficacy or safety profile.

Major Interactions (Avoid)

  • Beta‑blockers: may blunt compensatory tachycardia and exacerbate hypotension.
  • MAO inhibitors: increase risk of hypertensive crisis when combined with sympathomimetics.
  • Tricyclic antidepressants: potentiate vasoconstrictive effects, raising blood pressure excessively.

Moderate Interactions (Monitor Closely)

  • Calcium channel blockers: may enhance vasodilatory opposition, requiring dose adjustments.
  • Diuretics: alter intravascular volume, affecting pressor response.
  • Sedatives/anxiolytics: can mask signs of excessive vasoconstriction or hypertension.

Frequently Asked Questions

Mykronor contains noradrenaline tartrate and is employed in hospital settings as a potent vasopressor to raise blood pressure in patients with acute hypotension, septic shock, or cardiogenic shock. It is administered intravenously under continuous hemodynamic monitoring to stabilize circulation during critical illness.

Noradrenaline tartrate acts as a direct agonist at alpha‑1 adrenergic receptors on vascular smooth muscle. Activation causes calcium‑mediated contraction, producing vasoconstriction and increasing systemic vascular resistance, which elevates arterial pressure and improves organ perfusion in shock states.

The dosing regimen for Mykronor is individualized by the treating physician based on the patient’s hemodynamic status, target blood pressure, and response to therapy. Clinicians typically start with a low infusion rate and titrate upward while monitoring vital signs.

Safety data for noradrenaline tartrate in pregnancy and lactation are limited. It is generally reserved for situations where the potential benefit to the mother outweighs any possible risk to the fetus or infant, and its use should be decided by a qualified healthcare professional.

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

Compared with agents such as dopamine or phenylephrine, noradrenaline tartrate provides strong alpha‑adrenergic vasoconstriction with relatively modest beta‑adrenergic activity, making it effective for raising systemic vascular resistance while limiting tachycardia. Choice of pressor depends on the clinical scenario and physician preference.

Mykronor should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. Prior to use, the solution should be inspected for particulate matter and administered using aseptic technique.

Mykronor is supplied as an injectable solution for intravenous infusion. It is typically delivered through a calibrated infusion pump, allowing precise control of the infusion rate. Continuous blood pressure and cardiac monitoring are essential throughout administration.

Serious adverse events include cardiac arrhythmias, myocardial ischemia, severe hypertension, tissue necrosis from extravasation, and pulmonary edema. Prompt recognition and management of these complications are critical, and the drug should be titrated carefully under expert supervision.

Mykronor is contraindicated in patients with known hypersensitivity to noradrenaline or any component of the formulation, and it should be used with extreme caution in individuals with uncontrolled hypertension, severe peripheral vascular disease, or those at high risk for tissue ischemia.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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