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

Mykronor

Active Ingredient:
Noradrenaline Tartrate
Origin:
EU

Mykronor (Noradrenaline Tartrate)

Noradrenaline, the active ingredient in Mykronor, is a sympathomimetic amine presented as an injectable solution for intravenous use. It is employed in critical care to treat acute hypotension, septic shock, cardiogenic shock and cardiac arrest in hospitalized patients requiring rapid blood pressure support.

GNH India supplies Mykronor as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and intensive care units worldwide. The company adheres to stringent quality standards and provides regulatory documentation for import and distribution in EU and other markets.

Manufacturer / TM Owner

Laboratoire Aguettant

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Indications & Clinical Uses

  • Mykronor, a vasopressor acting on the adrenergic system, is indicated for several acute shock states.
  • Acute hypotension: raises systemic blood pressure to maintain organ perfusion.
  • Septic shock: restores vascular tone and supports circulation in severe infection.
  • Cardiogenic shock: improves cardiac output and systemic perfusion when the heart fails to pump effectively.
  • Cardiac arrest: provides vasoconstrictive support during resuscitation efforts.

How It Works

  • Noradrenaline acts as a direct agonist at α1‑adrenergic receptors on vascular smooth muscle, producing potent peripheral vasoconstriction that elevates systemic vascular resistance and arterial pressure. It also stimulates β1‑adrenergic receptors in the heart, modestly increasing heart rate and contractility, which together raise cardiac output. These actions are dose‑dependent and are rapidly reversible upon discontinuation.

Side Effects

Noradrenaline may produce a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Tachycardia: rapid increase in heart rate.
  • Hypertension: excessive rise in blood pressure.
  • Headache: pressure‑type head pain.

Serious or Rare Side Effects

  • Myocardial ischemia: reduced blood flow to heart muscle.
  • Cardiac arrest: sudden loss of heart function.
  • Tissue necrosis at infusion site: local tissue death due to extravasation.

Precautions & Warnings

  • When using Mykronor, clinicians should observe several safety precautions to minimize risks.
  • Cardiovascular monitoring: continuous blood pressure and heart‑rate monitoring is required.
  • Titration by experienced staff: dose should be adjusted gradually under specialist supervision.
  • Contraindication in uncontrolled hypertension: avoid use in patients with severely elevated baseline pressure.
  • Caution in myocardial ischemia: use only if benefits outweigh risk of reduced coronary perfusion.
  • Adjust in renal or hepatic impairment: monitor plasma levels and organ function closely.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Noradrenaline can interact with other medicines, influencing its pressor effect or causing adverse events.

Major Interactions (Avoid)

  • MAO inhibitors: risk of hypertensive crisis.
  • Tricyclic antidepressants: additive sympathomimetic effect leading to severe hypertension.
  • Other vasopressors (e.g., epinephrine): may cause excessive vasoconstriction.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may blunt the desired increase in cardiac output.
  • Calcium channel blockers: can enhance hypotensive episodes if dose is reduced.
  • Diuretics: may potentiate volume depletion and affect blood pressure response.
  • General anesthetics: may alter hemodynamic stability during surgery.

Frequently Asked Questions

Mykronor is an injectable vasopressor containing noradrenaline tartrate. It is used in hospital settings to raise blood pressure during acute hypotension, septic shock, cardiogenic shock and cardiac arrest, helping to restore adequate organ perfusion.

Noradrenaline acts as a direct agonist at α1‑adrenergic receptors, causing strong peripheral vasoconstriction that increases systemic vascular resistance. It also stimulates β1 receptors in the heart, modestly raising heart rate and contractility, together supporting blood pressure and cardiac output.

The dose of Mykronor is individualized. A qualified prescriber determines the starting infusion rate and titrates it based on the patient’s hemodynamic response, with adjustments made under continuous monitoring in an intensive‑care environment.

Safety data for noradrenaline in pregnancy and lactation are limited. It should only be used 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 Mykronor, submit an enquiry on the product page at gnhindia.com with 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.

Mykronor (noradrenaline) is a first‑line vasopressor for most shock states because of its potent α‑mediated vasoconstriction and modest β1 activity. Compared with dopamine, it has less tachyarrhythmic risk, and unlike epinephrine it produces less metabolic acidosis, making it preferred in many critical‑care protocols.

Mykronor must be stored at 2‑8 °C, protected from light, and kept in its original container. Do not freeze or shake the vial. Before use, inspect for particulate matter and ensure the solution is at room temperature if required by the administration protocol.

Mykronor is given by intravenous infusion. The solution is typically diluted in a compatible carrier fluid and administered through a calibrated infusion pump under the supervision of trained clinical staff, with continuous blood‑pressure and cardiac monitoring throughout the infusion.

The most serious adverse events include severe hypertension, myocardial ischemia or infarction, cardiac arrest, and tissue necrosis at the infusion site if extravasation occurs. Prompt recognition and immediate management of these events are essential during therapy.

Mykronor should be avoided in patients with uncontrolled hypertension, known hypersensitivity to noradrenaline or its excipients, and conditions such as pheochromocytoma where excessive catecholamine release could worsen the disease. Use only under specialist supervision in all other cases.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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