Product image of Noradrenalin Laboratoire Aguettant (Noradrenaline Tartrate) supplied by GNH India

Noradrenalin Laboratoire Aguettant

Active Ingredient:
Noradrenaline Tartrate
Origin:
EU

Noradrenalin Laboratoire Aguettant (Noradrenaline Tartrate)

Noradrenaline tartrate, the active ingredient in Noradrenalin Laboratoire Aguettant, is a sympathomimetic presented as an injectable solution for intravenous use. It is employed to increase systemic vascular resistance and raise arterial pressure in patients with acute hypotension, septic shock, or cardiogenic shock, particularly in intensive care and emergency settings where rapid hemodynamic support is required.

GNH India supplies Noradrenalin Laboratoire Aguettant as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, critical care units, clinics and procurement teams worldwide across the world.

Manufacturer / TM Owner

Laboratoire Aguettant

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Indications & Clinical Uses

Noradrenalin acts as a potent vasopressor targeting the sympathetic pathway to restore blood pressure in critical care.

  • Hypotension: raises arterial pressure by increasing systemic vascular resistance.
  • Septic shock: supports hemodynamics when vasodilatory failure leads to profound hypotension.
  • Cardiogenic shock: improves perfusion by augmenting afterload and maintaining coronary flow.

How It Works

  • Noradrenaline tartrate is a direct agonist of α1‑adrenergic receptors on vascular smooth muscle, causing vasoconstriction and an increase in systemic vascular resistance. It also stimulates β1‑adrenergic receptors in the heart, providing modest inotropic support. The combined α‑ and β‑effects raise mean arterial pressure and improve organ perfusion during states of distributive or cardiogenic shock. These actions are rapid and dose‑dependent, allowing clinicians to titrate the infusion to achieve target hemodynamic goals.

Side Effects

Noradrenalin may produce a range of adverse reactions, varying from frequent to rare but serious.

Common Side Effects

  • Tachycardia: increased heart rate due to β1 stimulation.
  • Headache: result of rapid blood pressure changes.
  • Anxiety or restlessness: central nervous system stimulation.
  • Peripheral ischemia: reduced blood flow to extremities.
  • Arrhythmias: ectopic beats or mild rhythm disturbances.

Serious or Rare Side Effects

  • Severe hypertension: excessive rise in blood pressure risking vascular injury.
  • Myocardial ischemia: reduced coronary perfusion from increased afterload.
  • Tissue necrosis at injection site: due to extravasation.
  • Cardiac arrest: rare but life‑threatening event.

Precautions & Warnings

When using Noradrenalin, clinicians should observe specific safety measures to minimize risks.

  • Monitor blood pressure: adjust infusion to maintain target MAP.
  • Assess cardiac function: avoid in uncontrolled tachyarrhythmias.
  • Use caution in peripheral vascular disease: risk of ischemia.
  • Prevent extravasation: ensure secure intravenous access.
  • Pregnancy and lactation: safety unknown; use only if benefits outweigh risks.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Noradrenalin can interact with several drug classes, requiring attention to avoid harmful effects.

Major Interactions (Avoid)

  • MAO inhibitors: risk of hypertensive crisis due to synergistic catecholamine effects.
  • Tricyclic antidepressants: additive pressor response may cause severe hypertension.
  • β‑blockers: may blunt compensatory tachycardia and alter hemodynamic response.

Moderate Interactions (Monitor Closely)

  • Vasodilators (e.g., nitroglycerin): may necessitate higher Noradrenalin doses.
  • Calcium channel blockers: can enhance hypotensive episodes if dose reduced.
  • General anesthetics: may affect vascular tone and require careful titration.

Frequently Asked Questions

Noradrenalin Laboratoire Aguettant contains noradrenaline tartrate, a vasopressor used in intensive‑care settings to raise blood pressure in patients with acute hypotension, septic shock or cardiogenic shock. It provides rapid vascular constriction and modest cardiac support to restore adequate organ perfusion.

Noradrenaline tartrate acts as a direct agonist at α1‑adrenergic receptors on vascular smooth muscle, causing vasoconstriction and increasing systemic vascular resistance. It also stimulates β1‑adrenergic receptors in the heart, giving a modest increase in contractility, together raising mean arterial pressure.

The dosage of Noradrenalin is individualized. A qualified prescriber determines the starting infusion rate and titrates it based on the patient’s blood pressure response, target mean arterial pressure, and overall clinical status. No fixed regimen is provided in public literature.

Safety data for noradrenaline in pregnancy and lactation are limited. The product is classified as having an unknown pregnancy category, so it should only be used when the potential maternal benefit justifies any possible risk to the fetus or infant.

To place an order, 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 where required) and any necessary import documentation.

Noradrenalin is the first‑line vasopressor for most forms of shock because of its potent α‑mediated vasoconstriction and limited β‑activity. Compared with dopamine, it produces less tachyarrhythmia, and unlike epinephrine it has a lower risk of increasing heart rate excessively, making it preferable for many critically ill patients.

The product must be stored refrigerated at 2 °C to 8 °C. Keep it in the original container, protect it from light, and avoid freezing or shaking. If the solution appears discolored or contains particles, it should not be used.

Noradrenalin is given exclusively by intravenous infusion, usually through a central venous catheter or a well‑secured peripheral line. The infusion is prepared in a compatible diluent and titrated continuously while monitoring blood pressure and heart rate.

The most critical adverse events include severe hypertension that can cause vascular injury, myocardial ischemia from increased afterload, tissue necrosis if the drug extravasates, and rare cases of cardiac arrest. Continuous hemodynamic monitoring is essential to detect these complications early.

Noradrenalin is contraindicated in patients with known hypersensitivity to the product, those with uncorrected pheochromocytoma, or individuals with severe peripheral or mesenteric ischemia where further vasoconstriction could worsen tissue damage.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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