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 agent presented as an injectable solution for intravenous use. It acts as a potent vasopressor, raising blood pressure by causing vasoconstriction and supporting cardiac output, and is employed in acute hypotension, septic shock, cardiogenic shock and cardiac arrest in critical care settings.

GNH India supplies Mykronor as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide, providing reliable sourcing for critical care medicines through established distribution networks.

Manufacturer / TM Owner

Laboratoire Aguettant

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Indications & Clinical Uses

  • Mykronor is a vasopressor used in critical care to restore circulatory stability in severe hypotensive states.
  • Acute hypotension: raises systemic vascular resistance to maintain organ perfusion.
  • Septic shock: improves blood pressure when fluid resuscitation alone is insufficient.
  • Cardiogenic shock: supports cardiac output and arterial pressure during heart failure.
  • Cardiac arrest: provides immediate pressor support during resuscitation efforts.

How It Works

  • Noradrenaline tartrate acts as a direct agonist at alpha‑1 adrenergic receptors, producing potent vasoconstriction and increasing systemic vascular resistance. At higher concentrations it also stimulates beta‑1 receptors, enhancing myocardial contractility and cardiac output. The combined alpha and beta activity rapidly elevates arterial pressure and improves organ perfusion, making it effective for reversing profound hypotension in shock states in critically ill patients.

Side Effects

Mykronor may be associated with several adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Tachycardia: increased heart rate due to beta‑1 stimulation.
  • Headache: vascular changes can provoke cranial discomfort.
  • Nausea: gastrointestinal upset may occur.
  • Peripheral ischemia: reduced blood flow to extremities.

Serious or Rare Side Effects

  • Severe hypertension: excessive blood pressure rise.
  • Myocardial ischemia: reduced coronary perfusion leading to chest pain.
  • Tissue necrosis at injection site: local vascular compromise.
  • Anaphylaxis: rare severe allergic reaction.

Precautions & Warnings

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

  • Cardiac monitoring: continuous ECG and blood pressure monitoring is required.
  • Dose titration: adjust infusion rate based on hemodynamic response.
  • Contraindications: avoid in patients with uncorrected hypovolemia.
  • Drug interactions: be aware of synergistic effects with other vasopressors.
  • Pregnancy and lactation: use only if benefits outweigh potential risks, as safety data are limited.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Mykronor can interact with other agents, influencing its pressor effect or causing adverse events.

Major Interactions (Avoid)

  • Phosphodiesterase inhibitors (e.g., milrinone): may cause profound hypotension.
  • Beta‑blockers: can blunt the beta‑1 mediated increase in cardiac output.
  • MAO inhibitors: increase risk of hypertensive crisis.

Moderate Interactions (Monitor Closely)

  • Other vasopressors (e.g., dopamine): may lead to excessive vasoconstriction.
  • Calcium channel blockers: may enhance vasoconstrictive effects.
  • Sedatives and anesthetics: may mask signs of hypertension.

Frequently Asked Questions

Mykronor is an injectable vasopressor indicated for the rapid restoration of blood pressure in patients with acute hypotension, septic shock, cardiogenic shock, and during cardiac arrest. It is used in intensive care and emergency settings where immediate circulatory support is required.

Noradrenaline tartrate acts as a direct agonist at alpha‑1 adrenergic receptors, causing strong vasoconstriction and raising systemic vascular resistance. At higher concentrations it also stimulates beta‑1 receptors, increasing heart contractility and cardiac output, together elevating arterial pressure.

The dose of Mykronor 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. Exact dosing regimens are not publicly disclosed.

Safety data for noradrenaline tartrate 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 under close medical supervision.

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 (including cold‑chain where needed) and import documentation.

Mykronor (noradrenaline) is often compared with dopamine or epinephrine. Noradrenaline provides more potent alpha‑mediated vasoconstriction with less tachycardia than dopamine, while epinephrine adds stronger beta‑2 effects that can increase metabolic demand. Choice depends on the clinical scenario and desired balance of vascular tone versus heart rate.

Mykronor should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the product in its original packaging until use and discard any solution that appears discolored or contains particles.

Mykronor is given by intravenous infusion. The solution is typically diluted in a compatible carrier fluid and administered through a calibrated infusion set. Continuous blood pressure and cardiac monitoring are required throughout the infusion, with dose adjustments made in real time.

Serious risks include severe hypertension, myocardial ischemia, tissue necrosis at the injection site, and rare anaphylactic reactions. Prompt recognition of excessive blood pressure rise, chest pain, or local tissue changes is essential, and immediate medical intervention should be initiated if these occur.

Mykronor is contraindicated in patients with uncorrected hypovolemia, known hypersensitivity to noradrenaline or its excipients, and in situations where excessive vasoconstriction could worsen tissue perfusion. Caution is also advised in patients with severe cardiac arrhythmias or uncontrolled hypertension.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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