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

Noradrenaline Aguettant

Active Ingredient:
Noradrenaline Tartrate
Origin:
EU

Noradrenaline Aguettant (Noradrenaline Tartrate)

Noradrenaline tartrate, the active ingredient in Noradrenaline Aguettant, is a sympathomimetic presented as an injectable solution for intravenous use. It acts on alpha‑adrenergic receptors to produce vasoconstriction, thereby increasing systemic vascular resistance and raising arterial pressure. Clinicians use it in emergency settings to treat severe hypotension associated with septic shock, cardiac arrest, and other critical circulatory failures.

GNH India supplies Noradrenaline Aguettant as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. The company adheres to European Union quality standards and provides regulatory documentation, cold‑chain logistics, and post‑market support for its cardiovascular agents.

Manufacturer / TM Owner

Laboratoire Aguettant

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Indications & Clinical Uses

Noradrenaline Aguettant is a sympathomimetic vasopressor used in acute cardiovascular emergencies.

  • Hypotension: Restores arterial pressure in patients with severe low blood pressure unresponsive to fluid resuscitation.
  • Septic shock: Improves hemodynamic stability by counteracting the vasodilatory effects of sepsis.
  • Cardiac arrest: Supports coronary perfusion during resuscitation efforts when other measures are insufficient.

How It Works

  • Noradrenaline tartrate acts as an agonist at alpha‑1 adrenergic receptors on vascular smooth muscle. Stimulation of these receptors triggers phosphatidylinositol‑mediated calcium influx, causing potent, significant vasoconstriction and an increase in systemic vascular resistance. The resulting rise in arterial pressure enhances organ perfusion during shock states. At higher concentrations, it may also stimulate beta‑1 receptors, modestly increasing heart rate and contractility.

Side Effects

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

Common Side Effects

  • Tachycardia: rapid increase in heart rate.
  • Arrhythmia: irregular cardiac rhythm.
  • Hypertension: elevated blood pressure beyond therapeutic target.
  • Headache: mild to moderate cranial pain.
  • Nausea: feeling of sickness or urge to vomit.

Serious or Rare Side Effects

  • Myocardial ischemia: reduced blood flow to heart muscle.
  • Severe hypertension: dangerous spikes in arterial pressure.
  • Peripheral ischemia: compromised blood flow to extremities.
  • Tissue necrosis at injection site: local cell death due to extravasation.
  • Anaphylaxis: severe allergic reaction with potential airway compromise.

Precautions & Warnings

When using Noradrenaline Aguettant, clinicians should observe specific precautions to minimize risks.

  • Blood pressure monitoring: continuously assess arterial pressure to avoid overshoot hypertension.
  • Cardiac monitoring: observe heart rhythm for tachyarrhythmias.
  • Dose titration: adjust infusion rate gradually based on hemodynamic response.
  • Renal impairment: use caution and consider lower initial rates in patients with reduced kidney function.
  • Contraindications: avoid in patients with known pheochromocytoma or severe hyperthyroidism.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Noradrenaline Aguettant can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • MAO inhibitors: risk of hypertensive crisis due to synergistic catecholamine effects.
  • Tricyclic antidepressants: may potentiate vasoconstriction and hypertension.
  • Ergot alkaloids: combined use can cause severe peripheral ischemia.
  • Beta‑blockers: may blunt desired cardiac response and increase risk of bradycardia.

Moderate Interactions (Monitor Closely)

  • Other vasopressors (e.g., phenylephrine): additive pressor effects may require dose reduction.
  • Anesthetic agents (e.g., halothane): can enhance cardiovascular instability.
  • Diuretics: may exacerbate intravascular volume depletion.
  • Calcium channel blockers: may interfere with vascular tone regulation.

Frequently Asked Questions

Noradrenaline Aguettant is indicated for the rapid correction of severe hypotension in emergency situations such as septic shock, cardiogenic shock, and cardiac arrest. It is used when blood pressure remains low despite adequate fluid resuscitation, helping to restore perfusion to vital organs.

Noradrenaline tartrate acts as an agonist at alpha‑1 adrenergic receptors on vascular smooth muscle, causing potent vasoconstriction and an increase in systemic vascular resistance. This raises arterial pressure. At higher concentrations it can also stimulate beta‑1 receptors, modestly increasing heart rate and contractility.

The dose of Noradrenaline Aguettant is individualized by the prescribing clinician. It is typically started as a low‑rate intravenous infusion and titrated upward based on continuous blood‑pressure monitoring and the patient’s hemodynamic response. Exact dosing regimens are not standardized and must follow local protocols.

Safety data for noradrenaline in pregnancy and lactation are limited. The drug is generally avoided unless the potential maternal benefit outweighs possible fetal risk. Breastfeeding mothers should consult their healthcare provider, as noradrenaline may be excreted in milk and could affect the 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.

Noradrenaline is a first‑line vasopressor because of its strong alpha‑adrenergic activity and relatively modest beta‑adrenergic effects, providing reliable blood‑pressure support with less tachycardia than dopamine. Compared with epinephrine, it causes less increase in heart rate and myocardial oxygen consumption, making it preferable in many shock states.

Noradrenaline Aguettant should be stored in a refrigerated environment between 2 °C and 8 °C. The vials must be kept in their original packaging, protected from light, and should never be frozen or shaken. If the product reaches room temperature, it should be used promptly or returned to refrigeration.

The medication is given by intravenous infusion. It is usually diluted in a compatible carrier solution and administered through a calibrated infusion pump to allow precise rate adjustments. Continuous hemodynamic monitoring is essential during administration to ensure the desired blood‑pressure response and to detect adverse effects early.

Serious risks include severe hypertension that can lead to vascular injury, myocardial ischemia due to increased afterload, peripheral ischemia or tissue necrosis from extravasation, and rare anaphylactic reactions. Prompt recognition and management of these events are critical, and infusion rates should be adjusted or stopped as needed.

Noradrenaline Aguettant is contraindicated in patients with known pheochromocytoma, severe hyperthyroidism, or uncontrolled hypertension. Caution is also advised in individuals with significant peripheral vascular disease, recent myocardial infarction, or those receiving MAO inhibitors, as the drug may exacerbate these conditions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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