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

Noradrenalin Noridem

Active Ingredient:
Noradrenaline Tartrate
Origin:
EU

Noradrenalin Noridem (Noradrenaline Tartrate)

Noradrenaline Tartrate, the active ingredient in Noradrenalin Noridem, is a sympathomimetic (vasopressor) presented as an injection solution for intravenous use. It is employed to raise blood pressure in acute hypotensive states, septic shock, cardiogenic shock, and as an adjunct in cardiac arrest.

GNH India supplies Noradrenalin Noridem as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Noridem Enterprises Ltd

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Indications & Clinical Uses

  • Noradrenalin Noridem acts on the sympathetic vascular system to restore hemodynamic stability in critical care settings.
  • Acute hypotension: raises systemic vascular resistance to improve blood pressure.
  • Septic shock: counteracts vasodilatory failure and supports organ perfusion.
  • Cardiogenic shock: provides vasoconstriction to augment coronary perfusion pressure.
  • Cardiac arrest (adjunct therapy): sustains arterial pressure during resuscitation efforts.

How It Works

  • Noradrenaline Tartrate is an alpha‑adrenergic receptor agonist that stimulates vascular smooth‑muscle alpha‑1 receptors, causing potent vasoconstriction and increased systemic vascular resistance. The resulting rise in arterial pressure improves organ perfusion. It also has modest beta‑1 activity, contributing to a slight increase in cardiac output, but its primary effect is vascular tone elevation.

Side Effects

Adverse reactions may arise from excessive vasoconstriction or catecholamine excess.

Common Side Effects

  • Hypertension: elevated systolic and diastolic pressures.
  • Tachycardia: increased heart rate due to beta‑1 stimulation.
  • Headache: secondary to rapid blood pressure changes.
  • Nausea or vomiting: gastrointestinal discomfort.
  • Peripheral ischemia: reduced blood flow to extremities.

Serious or Rare Side Effects

  • Cardiac arrhythmias: potentially life‑threatening rhythm disturbances.
  • Myocardial ischemia: reduced coronary blood flow leading to chest pain.
  • Severe hypertension: risk of cerebrovascular hemorrhage.
  • Tissue necrosis at extravasation sites: local tissue damage if the solution leaks outside the vein.

Precautions & Warnings

  • Clinicians should observe specific safety measures when using this vasopressor.
  • Cardiovascular monitoring: continuous blood pressure and heart‑rate tracking is required.
  • Dose titration: adjust infusion rate to achieve target pressure while avoiding overshoot.
  • Contraindications: avoid in patients with known hypersensitivity to norepinephrine.
  • Arrhythmia caution: use carefully in individuals with pre‑existing cardiac rhythm disorders.
  • Extravasation risk: ensure proper IV placement and monitor infusion site.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Noradrenaline Tartrate can interact with several drug classes, influencing its hemodynamic effects.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): may cause hypertensive crisis.
  • Other sympathomimetics (e.g., epinephrine): additive vasoconstriction can lead to severe hypertension.

Moderate Interactions (Monitor Closely)

  • Vasodilators (e.g., nitroglycerin): may blunt norepinephrine’s pressor effect.
  • ACE inhibitors or ARBs: can alter blood pressure response.
  • Calcium channel blockers: may affect vascular tone and require dose adjustments.
  • Diuretics: volume status changes may modify required norepinephrine dose.

Frequently Asked Questions

Noradrenalin Noridem is an intravenous vasopressor used in critical care to treat acute hypotension, septic shock, cardiogenic shock, and as an adjunct therapy during cardiac arrest. It works by constricting blood vessels to raise systemic blood pressure and improve organ perfusion.

Noradrenaline Tartrate acts as an alpha‑adrenergic receptor agonist. By stimulating alpha‑1 receptors on vascular smooth muscle, it causes potent vasoconstriction, increasing systemic vascular resistance and arterial pressure. It also has modest beta‑1 activity that can modestly raise cardiac output.

The dosage and infusion rate of Noradrenalin Noridem are determined by the prescribing clinician based on the patient’s hemodynamic status, target blood pressure, and response to therapy. Dosing is individualized and titrated to achieve the desired clinical effect.

The safety of Noradrenalin Noridem during pregnancy or lactation has not been established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by the treating physician.

To 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 needed), and import documentation.

Noradrenalin Noridem is the first‑line vasopressor for many shock states due to its strong alpha‑1 mediated vasoconstriction and relatively predictable hemodynamic profile. Compared with agents like dopamine or phenylephrine, it offers more consistent blood pressure support with fewer arrhythmic effects, making it a preferred choice in most guidelines.

The product should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Before use, inspect the vial for particulate matter or discoloration and ensure aseptic technique during preparation and administration.

Noradrenalin Noridem is supplied as an injectable solution for intravenous infusion. It is typically administered via a calibrated infusion pump, with the rate adjusted according to continuous blood pressure monitoring to achieve the desired hemodynamic target.

Serious risks include severe hypertension, cardiac arrhythmias, myocardial ischemia, and tissue necrosis if extravasation occurs. Continuous cardiovascular monitoring is essential to detect and manage these complications promptly.

Patients with known hypersensitivity to norepinephrine or its excipients should not receive the product. Caution is also advised in individuals with uncontrolled tachyarrhythmias, severe peripheral vascular disease, or those at high risk for tissue ischemia.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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