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 amine presented as an injectable solution for intravenous use. It is employed to raise blood pressure in patients experiencing acute hypotension, septic shock, cardiogenic shock, or anesthesia‑induced hypotension, typically in intensive care or operative settings.

GNH India supplies Mykronor as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. The product meets EU marketing authorization standards and is manufactured under GMP conditions, ensuring consistent potency and safety for clinical use.

Manufacturer / TM Owner

Laboratoire Aguettant

1
Pack/s
This product is added to your enquiry list

Request a Quote

Please fill out the form below and our team will get back to you shortly with pricing and further information.

A minimum order value applies. Our team will confirm the exact amount or quantity after reviewing your requirements.

Indications & Clinical Uses

  • Mykronor, a vasopressor acting on the adrenergic system, is indicated for several acute shock states.
  • Acute hypotension: restores systemic blood pressure in patients with sudden drops in arterial pressure.
  • Septic shock: improves hemodynamic stability during severe infection‑related circulatory failure.
  • Cardiogenic shock: supports cardiac output when the heart cannot maintain adequate perfusion.
  • Anesthesia‑induced hypotension: counteracts blood pressure reductions caused by anesthetic agents during surgery.

How It Works

  • Noradrenaline tartrate acts as an agonist at α1‑adrenergic receptors, producing peripheral vasoconstriction that raises systemic vascular resistance. It also stimulates β1‑adrenergic receptors modestly, enhancing myocardial contractility and cardiac output. The combined α‑mediated vasoconstriction and β‑mediated inotropic effect increase arterial pressure, making it useful for rapid correction of hypotensive states.

Side Effects

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

Common Side Effects

  • Tachycardia: increased heart rate.
  • Headache: pressure sensation in the head.
  • Nausea: feeling of sickness.
  • Peripheral ischemia: reduced blood flow to extremities.
  • Anxiety: heightened nervousness or restlessness.

Serious or Rare Side Effects

  • Severe hypertension: dangerously high blood pressure.
  • Arrhythmias: abnormal heart rhythms including ventricular tachycardia.
  • Myocardial ischemia: reduced blood flow to heart muscle.
  • Limb necrosis: tissue death due to extreme vasoconstriction.
  • Pulmonary edema: fluid accumulation in lungs.

Precautions & Warnings

Prior to using Mykronor, clinicians should consider several safety considerations to minimize risk.

  • Cardiac disease: monitor for ischemia and arrhythmias.
  • Peripheral vascular disease: avoid excessive dosing that may worsen limb perfusion.
  • Severe hypertension: titrate carefully to prevent dangerous pressure spikes.
  • Pregnancy and lactation: use only if benefits outweigh potential risks, as safety data are limited.
  • Concomitant MAO inhibitors: discontinue to reduce risk of hypertensive crisis.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Mykronor can interact with other agents that affect cardiovascular tone or catecholamine metabolism.

Major Interactions (Avoid)

  • MAO inhibitors: risk of severe hypertension.
  • Tricyclic antidepressants: additive pressor effects.
  • Beta‑blockers: may blunt desired increase in cardiac output.
  • Vasopressin: excessive vasoconstriction.
  • Calcium channel blockers: unpredictable blood pressure responses.

Moderate Interactions (Monitor Closely)

  • General anesthetics: may potentiate hypotensive episodes.
  • Diuretics: can alter intravascular volume affecting response.
  • ACE inhibitors: may reduce effectiveness of blood pressure support.

Frequently Asked Questions

Mykronor is an intravenous vasopressor indicated for the rapid correction of low blood pressure in acute hypotension, septic shock, cardiogenic shock, and anesthesia‑induced hypotension. It is used in hospital settings such as intensive care units and operating rooms to support circulatory function.

Noradrenaline tartrate stimulates α1‑adrenergic receptors, causing peripheral blood‑vessel constriction that raises systemic vascular resistance. It also modestly activates β1‑adrenergic receptors, increasing heart‑muscle contractility. The combined effect elevates arterial pressure and improves organ perfusion during shock states.

The dosage of Mykronor is individualized and determined by the prescribing clinician based on the patient’s condition, response, and monitoring parameters. Specific dosing regimens are not provided here and should follow the prescribing information and institutional protocols.

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 the decision must be made by the treating physician.

To order Mykronor, submit an enquiry on the 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 (including cold‑chain if needed), and import documentation.

Mykronor (noradrenaline) provides both α‑mediated vasoconstriction and modest β1‑stimulation, offering a balanced increase in blood pressure and cardiac output. Compared with pure α‑agonists like phenylephrine, it may better support heart function, while agents such as dopamine have more variable receptor activity and dose‑dependent effects.

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

Mykronor is administered intravenously, typically as a continuous infusion. The infusion rate is adjusted according to the patient’s blood pressure response and monitored continuously in a critical‑care setting. Dilution and infusion set specifications are provided in the product’s prescribing information.

Serious risks include severe hypertension, life‑threatening arrhythmias, myocardial ischemia, and peripheral tissue necrosis due to excessive vasoconstriction. Continuous hemodynamic monitoring is essential to detect and manage these complications promptly.

Mykronor is contraindicated in patients with known hypersensitivity to noradrenaline or any excipients in the formulation. Caution is advised in individuals with uncontrolled severe hypertension, recent myocardial infarction, or severe peripheral vascular disease, where the drug’s vasoconstrictive effects may be harmful.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

Disclaimer

At GNH India, we aim to provide information that is expert-reviewed, accurate, and reliable. However, all content on this platform is intended for general informational purposes only and does not constitute professional medical advice, diagnosis, or treatment. While efforts are made to maintain accuracy and currency, the information may contain errors, omissions, or may not reflect the latest developments. Always consult a qualified healthcare professional regarding any medical concerns.

All product names, brand names, trademarks and registered trademarks displayed on this website are the property of their respective owners. This website and its operator are not affiliated with, endorsed by, or authorized by any such trade mark owners unless expressly stated. Any reference to product names or trademarks is made solely for descriptive and informational purposes. No commercial relationship, sponsorship, approval, or association with any trademark owner should be inferred. Information provided herein does not constitute promotion, advertising, or an offer for sale of any medicinal product and is intended solely for general informational purposes.

All trademarks and brand names displayed on this website are used strictly in accordance with the provisions of the Trade Marks Act, 1999, specifically Sections 30 and 30(1) governing fair use. Trademark ownership has been accurately attributed under the "Manufacturer/ TM Owner" section in compliance with statutory requirements.

Ordering Process

Simple, Secure, and Seamless

Learn how our streamlined ordering process guarantees fast, compliant, and reliable access to essential medicines worldwide.

Quote request form

01

Submit Quote Request Form

Tell us what medications you need by filling out our simple form and uploading a valid document.

Price estimate review

02

We Review & Send Estimate

Our licensed pharmacists will verify your details and provide you with a detailed cost estimate.

Secure payment

03

Confirm & Make Payment

Discuss any queries, approve the estimate, and complete your payment.

Worldwide delivery

04

Get Delivered

Your medicines, safely packed and delivered to your door or nearest airport — hassle-free.

Quality You Can Trust

Our internationally recognized certifications underscore our commitment to safety, quality, and excellence.