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 a solution for injection for intravenous use. Approved in the European Union, it is used to raise blood pressure and improve cardiac output in patients with severe hypotension, shock, or cardiac arrest.

GNH India supplies Noradrenalin Laboratoire Aguettant as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Laboratoire Aguettant

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Indications & Clinical Uses

Noradrenalin is a vasopressor that acts on the sympathetic cardiovascular pathway to restore adequate perfusion in critical care settings.

  • Hypotension: restores arterial pressure when conventional fluids are insufficient.
  • Shock (septic, cardiogenic, or hemorrhagic): supports systemic vascular resistance and cardiac output.
  • Cardiac arrest: provides immediate pressor support during advanced life‑saving measures.

How It Works

  • Noradrenaline tartrate acts as a direct agonist at alpha‑1 and beta‑1 adrenergic receptors. Stimulation of alpha‑1 receptors causes peripheral vasoconstriction, increasing systemic vascular resistance, while beta‑1 activation enhances myocardial contractility and heart rate, together raising arterial pressure and cardiac output in acute circulatory failure.

Side Effects

Noradrenalin may be associated with a range of adverse reactions that require monitoring.

Common Side Effects

  • Tachycardia: rapid heart rate due to beta‑1 stimulation.
  • Headache: result of sudden vascular changes.
  • Nausea: gastrointestinal upset.
  • Anxiety or restlessness: central sympathomimetic effect.
  • Peripheral ischemia: reduced blood flow to extremities.
  • Extravasation pain: local irritation if the solution leaks from the vein.

Serious or Rare Side Effects

  • Severe hypertension: excessive rise in blood pressure.
  • Myocardial ischemia: reduced coronary perfusion.
  • Life‑threatening arrhythmias: ventricular tachycardia or fibrillation.
  • Tissue necrosis: from extravasation injury.
  • Pulmonary edema: fluid accumulation in lungs.
  • Acute limb ischemia: critical loss of blood flow.

Precautions & Warnings

Use of Noradrenalin requires careful clinical oversight and adherence to safety protocols.

  • Blood pressure monitoring: continuously observe arterial pressure and adjust infusion rate.
  • Cardiac monitoring: watch for arrhythmias and ischemic changes.
  • Central venous access: preferred to reduce extravasation risk.
  • Dose titration: start low and increase gradually based on response.
  • Contraindication in pheochromocytoma: avoid use due to risk of hypertensive crisis.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Noradrenalin can interact with several drug classes, influencing its pressor effect and safety profile.

Major Interactions (Avoid)

  • MAO inhibitors: may cause hypertensive emergencies.
  • Tricyclic antidepressants: potentiate vasoconstriction.
  • Beta‑blockers: blunt beta‑1 mediated cardiac effects.
  • Other vasopressors: risk of excessive vasoconstriction.
  • Monoamine oxidase inhibitors: synergistic pressor response.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors: may attenuate pressor response.
  • Diuretics: affect intravascular volume and response.
  • Calcium channel blockers: can modify vascular tone.
  • Anesthetic agents: may enhance hypotensive effects.
  • Sedatives: may mask signs of excessive hypertension.

Frequently Asked Questions

Noradrenalin Laboratoire Aguettant is an injectable vasopressor used in acute care to raise blood pressure and improve cardiac output in patients with severe hypotension, various forms of shock, or cardiac arrest when rapid circulatory support is required.

Noradrenaline tartrate directly stimulates alpha‑1 receptors, causing peripheral vasoconstriction, and beta‑1 receptors, increasing heart contractility and rate. This combined action elevates systemic vascular resistance and cardiac output, helping restore adequate tissue perfusion.

The dose of Noradrenalin is individualized. A qualified prescriber determines the infusion rate based on the patient’s hemodynamic status, target blood pressure, and response, and adjusts it continuously during therapy.

The safety of noradrenaline in pregnancy or lactation has not been established. It should be used only if the potential benefit justifies any potential risk to the fetus or infant, and under close medical supervision.

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 import documentation.

Noradrenalin is the first‑line vasopressor for most shock states because of its balanced alpha‑1 and beta‑1 activity. Compared with dopamine, it has less tachyarrhythmic risk, and unlike phenylephrine, it also supports cardiac output through beta‑1 stimulation.

Store the solution for injection at 2‑8 °C, protected from light. Do not freeze or shake the vial. Keep it in the original packaging until use to maintain stability.

The drug is supplied as a sterile solution for intravenous injection. It is typically administered via a controlled infusion pump, allowing precise titration of the dose to achieve the desired hemodynamic response.

Serious risks include severe hypertension, myocardial ischemia, life‑threatening arrhythmias, tissue necrosis from extravasation, and acute limb ischemia. Continuous monitoring of cardiovascular status is essential to detect and manage these complications promptly.

Patients with known hypersensitivity to noradrenaline or its excipients, those with pheochromocytoma, or individuals in whom uncontrolled hypertension would pose a significant risk should not receive this medication.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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