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

Norasalf

Active Ingredient:
Noradrenaline Tartrate
Origin:
EU

Norasalf (Noradrenaline Tartrate)

Noradrenaline tartrate, the active ingredient in Norasalf, is a sympathomimetic presented as a sterile solution for injection for intravenous use. It is employed to rapidly raise blood pressure in patients experiencing severe hypotension, septic shock, or cardiogenic shock, particularly in intensive care and emergency environments.

GNH India supplies Norasalf as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and clinics worldwide, providing regulatory‑approved product for critical care applications. The company ensures timely delivery across EU and other regulated markets.

Manufacturer / TM Owner

S.A.L.F. Spa Laboratorio Farmacologico

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Indications & Clinical Uses

Noradrenaline tartrate acts on the sympathetic vascular pathway to support circulatory function in critical care.

  • Hypotension: rapidly raises arterial pressure, helping to maintain adequate organ perfusion during acute drops in blood pressure.
  • Septic shock: counteracts profound vasodilation by increasing systemic vascular resistance, thereby improving hemodynamic stability in severe infection‑related shock.
  • Cardiogenic shock: augments afterload and supports blood pressure, assisting the failing heart to deliver sufficient circulation.

How It Works

  • Noradrenaline tartrate exerts its vasopressor effect by binding to α1‑adrenergic receptors on vascular smooth muscle, triggering phospholipase C activation and intracellular calcium release. This cascade induces potent vasoconstriction, elevating systemic vascular resistance and arterial pressure. At higher concentrations, it also stimulates β1‑adrenergic receptors in the heart, modestly increasing contractility and heart rate, further supporting circulatory output. The overall result is a swift increase in mean arterial pressure, essential for resuscitation.

Side Effects

Noradrenaline tartrate may be associated with a range of adverse reactions, varying from transient to life‑threatening.

Common Side Effects

  • Headache: mild to moderate headache during infusion.
  • Tremor: transient muscular tremor or shivering.
  • Nausea: occasional nausea or vomiting.
  • Palpitations: feeling of rapid or irregular heartbeat.

Serious or Rare Side Effects

  • Ischemia: reduced blood flow leading to myocardial or peripheral ischemic events.
  • Arrhythmias: potentially dangerous heart rhythm disturbances.
  • Extravasation: tissue injury if the solution leaks into surrounding tissue.
  • Lactic acidosis: rare metabolic disturbance.

Precautions & Warnings

When using Noradrenaline tartrate, clinicians should observe specific precautions to minimize risks and ensure therapeutic effectiveness.

  • Dose titration: adjust infusion rate to achieve target blood pressure while avoiding excessive vasoconstriction.
  • Monitoring: continuously monitor arterial pressure, heart rate, and cardiac rhythm during administration.
  • Fluid status: assess intravascular volume to prevent ischemia from excessive vasoconstriction.
  • Drug compatibility: avoid mixing with solutions containing calcium or bicarbonate to prevent precipitation.
  • Contraindications: do not use in patients with known hypersensitivity to catecholamines.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Noradrenaline tartrate can interact with several agents, altering its hemodynamic effects or safety profile.

Major Interactions (Avoid)

  • Beta‑blockers: may blunt the desired increase in cardiac output and cause severe hypotension.
  • MAO inhibitors: risk of hypertensive crisis due to excessive catecholamine activity.

Moderate Interactions (Monitor Closely)

  • Vasodilators (e.g., nitroglycerin): may require higher noradrenaline doses to maintain pressure.
  • Diuretics: can exacerbate hypovolemia, increasing risk of tissue ischemia.
  • General anesthetics: may potentiate cardiovascular depression, necessitating careful titration.

Frequently Asked Questions

Norasalf contains noradrenaline tartrate and is used as a vasopressor in acute care settings to treat severe hypotension, septic shock, and cardiogenic shock. It helps raise systemic vascular resistance and blood pressure, supporting organ perfusion during life‑threatening circulatory collapse.

Noradrenaline tartrate stimulates α1‑adrenergic receptors on vascular smooth muscle, causing vasoconstriction and an increase in systemic vascular resistance. At higher concentrations it also activates β1‑adrenergic receptors in the heart, modestly enhancing contractility and heart rate, together producing a rapid rise in arterial pressure.

The dose of Norasalf is individualized by the prescribing clinician. It is administered as an intravenous infusion that is titrated to the patient’s target mean arterial pressure, with the infusion rate adjusted based on continuous hemodynamic monitoring.

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 a qualified healthcare professional.

To order Norasalf, 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 necessary import documentation.

Norasalf (noradrenaline) is a first‑line vasopressor for most shock states because of its potent α‑adrenergic vasoconstriction and modest β‑adrenergic activity. Compared with dopamine, it has a lower risk of tachyarrhythmias, and unlike epinephrine it produces less metabolic waste and fewer hyperglycemic effects, making it preferred in many intensive‑care protocols.

Norasalf should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. The solution should be kept in its original sealed container until use, and any unused portion should be discarded according to local regulations.

Norasalf is supplied as a sterile solution for injection and is administered intravenously, usually via a central venous catheter. The infusion is started at a low rate and titrated upward while continuously monitoring blood pressure, heart rate, and cardiac rhythm.

Serious risks include severe hypertension, myocardial or peripheral ischemia, life‑threatening arrhythmias, and tissue injury from extravasation. Continuous hemodynamic monitoring and careful dose titration are essential to detect and manage these complications promptly.

Norasalf is contraindicated in patients with known hypersensitivity to noradrenaline or any of its excipients. Caution is also advised in individuals with severe peripheral vascular disease, uncontrolled tachyarrhythmias, or those receiving MAO inhibitors, where the drug may precipitate dangerous hypertensive events.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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