Product image of Noradrenalină Tartrat Hypericum (Noradrenaline Tartrate) supplied by GNH India

Noradrenalină Tartrat Hypericum

Active Ingredient:
Noradrenaline Tartrate
Origin:
EU

Noradrenalină Tartrat Hypericum (Noradrenaline Tartrate)

Noradrenaline tartrate, the active ingredient in Noradrenalină Tartrat Hypericum, is a sympathomimetic (alpha‑adrenergic agonist) presented as an intravenous solution for intravenous use. It is employed to raise blood pressure in patients with acute hypotension, septic shock, cardiogenic shock, or cardiac arrest.
GNH India supplies Noradrenalină Tartrat Hypericum as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Hypericum Srl

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Indications & Clinical Uses

Noradrenaline tartrate acts as a potent vasopressor in critical‑care settings, targeting severe hypotensive states.

  • Acute hypotension: restores systemic vascular resistance and improves perfusion pressure.
  • Septic shock: counteracts vasodilatory failure to maintain mean arterial pressure.
  • Cardiogenic shock: supports cardiac output by increasing afterload when needed.
  • Cardiac arrest: provides immediate pressor support during resuscitation efforts.

How It Works

  • Noradrenaline tartrate binds directly to alpha‑adrenergic receptors on vascular smooth muscle, causing vasoconstriction that elevates systemic vascular resistance and arterial pressure. The resulting increase in preload and afterload helps sustain organ perfusion during states of profound hypotension. Its activity is rapid, dose‑dependent, and reversible upon discontinuation.

Side Effects

Adverse reactions may occur with intravenous administration of noradrenaline tartrate.

Common Side Effects

  • Hypertension: excessive rise in blood pressure.
  • Tachycardia: increased heart rate due to reflex mechanisms.
  • Headache: pressure changes in cerebral vessels.
  • Peripheral ischemia: reduced blood flow to extremities.
  • Extravasation injury: local tissue damage if the infusion leaks.

Serious or Rare Side Effects

  • Cardiac arrhythmias: potentially life‑threatening rhythm disturbances.
  • Myocardial ischemia: reduced coronary perfusion from high afterload.
  • Tissue necrosis: severe extravasation leading to gangrene.
  • Severe hypertension crisis: dangerously high arterial pressure.

Precautions & Warnings

When using noradrenaline tartrate, clinicians should observe several safety measures.

  • Blood pressure monitoring: titrate infusion to maintain target MAP.
  • Cardiac rhythm observation: watch for arrhythmias, especially in patients with pre‑existing heart disease.
  • Dose titration: adjust slowly to avoid abrupt hypertension.
  • Extravasation risk: use central venous access whenever possible.
  • Peripheral vascular disease: use with caution due to risk of ischemia.
  • 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, requiring attention to avoid harmful effects.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): risk of hypertensive crisis.
  • Tricyclic antidepressants: additive pressor effect leading to severe hypertension.
  • Other vasopressors (e.g., phenylephrine): may cause excessive vasoconstriction.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may blunt tachycardia but increase afterload.
  • Calcium channel blockers: can enhance hypotensive episodes if dose is reduced.
  • ACE inhibitors or ARBs: may alter vascular response, requiring careful titration.

Frequently Asked Questions

Noradrenalină Tartrat Hypericum contains noradrenaline tartrate, a vasopressor used in hospital settings to treat acute hypotension, septic shock, cardiogenic shock, and cardiac arrest by raising systemic blood pressure and improving organ perfusion.

Noradrenaline tartrate acts as a direct agonist at alpha‑adrenergic receptors on vascular smooth muscle, causing vasoconstriction. This increases systemic vascular resistance, elevating arterial pressure and supporting blood flow to vital organs during severe hypotensive states.

The dose of noradrenaline tartrate is individualized by the treating physician. It is administered intravenously and titrated to achieve the desired blood pressure target, with the exact infusion rate determined by the patient’s clinical response.

Safety data for noradrenaline tartrate in pregnancy and lactation are limited. It should only be used when the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by the prescribing clinician.

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 if needed), and import documentation.

Noradrenaline tartrate is the first‑line vasopressor for most shock states due to its potent alpha‑adrenergic activity and relatively predictable effect on blood pressure. Alternatives such as phenylephrine or dopamine have different receptor profiles and may be chosen based on specific patient factors.

The product should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the vial in its original packaging until use and follow aseptic techniques during preparation and administration.

Noradrenaline tartrate is given by intravenous infusion, usually through a central venous catheter. The infusion is started at a low rate and titrated based on the patient’s blood pressure and clinical response, with continuous monitoring.

Serious risks include severe hypertension, cardiac arrhythmias, myocardial ischemia, peripheral ischemia leading to tissue necrosis, and extravasation injury. Prompt recognition and management of these events are essential during therapy.

Patients with known hypersensitivity to noradrenaline or any component of the formulation should not receive the drug. Caution is advised in individuals with severe peripheral vascular disease, uncontrolled hypertension, or those receiving MAO inhibitors.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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