Product image of Neoton (Phosphocreatine Sodium) supplied by GNH India

Neoton

Active Ingredient:
Phosphocreatine Sodium
Origin:
EU

Neoton (Phosphocreatine Sodium)

Phosphocreatine sodium, the active ingredient in Neoton, is an energy metabolism agent presented as an intravenous solution for intravenous use. It supports cardiac energy metabolism and is used in cardiovascular care to help maintain myocardial ATP levels.
GNH India supplies Neoton as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Alfasigma S.P.A.

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Indications & Clinical Uses

Neoton is employed in cardiovascular medicine to support myocardial energy metabolism and improve cardiac function.

  • Acute myocardial infarction: helps restore ATP levels in ischemic heart muscle.
  • Chronic heart failure: assists in maintaining cardiac contractility during decompensation.
  • Cardiac surgery: provides myocardial protection during cardiopulmonary bypass and reperfusion.

How It Works

  • Phosphocreatine sodium delivers phosphate groups directly to myocardial cells, where they combine with ADP to regenerate ATP via the creatine kinase reaction. By replenishing intracellular ATP stores, the drug sustains energy‑dependent processes such as ion transport and contractile function, thereby supporting cardiac performance during ischemic stress or surgical intervention.

Side Effects

Phosphocreatine sodium may be associated with a range of adverse reactions.

Common Side Effects

  • Injection site pain: mild discomfort at the infusion site.
  • Hypotension: transient drop in blood pressure during administration.
  • Nausea: occasional feeling of queasiness.
  • Headache: mild to moderate headache.
  • Flushing: transient skin reddening.
  • Dizziness: light‑headed sensation.

Serious or Rare Side Effects

  • Arrhythmia: abnormal heart rhythm, especially with high doses.
  • Myocardial ischemia: worsening of heart muscle oxygen deficiency.
  • Anaphylactic reaction: severe allergic response requiring immediate treatment.
  • Hyperkalemia: elevated blood potassium levels.
  • Severe hypotension: marked blood pressure fall needing intervention.

Precautions & Warnings

When using Neoton, clinicians should consider several safety measures.

  • Cardiac monitoring: observe rhythm and hemodynamics during infusion.
  • Electrolyte balance: check serum potassium and calcium before and after dosing.
  • Renal function: assess kidney function as impaired clearance may affect drug levels.
  • Concomitant inotropes: adjust doses of other cardiac stimulants to avoid excess activity.
  • Pregnancy and lactation: use only if benefits outweigh potential risks, as data are limited.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Phosphocreatine sodium can interact with other cardiovascular agents, requiring careful management.

Major Interactions (Avoid)

  • Concurrent high‑dose inotropes: may increase risk of arrhythmia.
  • Potassium‑sparing diuretics: can exacerbate hyperkalemia.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may blunt desired inotropic effect.
  • Calcium channel blockers: potential additive hypotensive effect.
  • ACE inhibitors or ARBs: monitor blood pressure and renal function.
  • Nitrates: watch for excessive vasodilation.
  • Anticoagulants: observe for bleeding if hemodynamic changes occur.

Frequently Asked Questions

Neoton is an intravenous formulation of phosphocreatine sodium used to support myocardial energy metabolism in conditions such as acute myocardial infarction, chronic heart failure, and during cardiac surgery to protect the heart muscle.

Phosphocreatine sodium supplies phosphate groups that combine with ADP to rapidly regenerate ATP within heart cells via the creatine kinase pathway, helping maintain energy supply during ischemic stress or surgical procedures.

The dose of Neoton is determined by the prescribing clinician based on the patient’s clinical condition, weight, and therapeutic goals. Specific dosing regimens are individualized and not standardized.

Safety data for phosphocreatine sodium in pregnancy and lactation are limited. It should be used only if the potential benefit justifies any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

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 if needed), and import documentation.

Neoton delivers phosphate directly for ATP regeneration, whereas other agents such as carnitine or coenzyme Q10 act indirectly on mitochondrial pathways. Neoton’s intravenous route provides rapid availability, making it suitable for acute settings like surgery or myocardial infarction.

Neoton should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the product in its original packaging to maintain stability.

Neoton is given as an intravenous infusion under medical supervision. The infusion rate and duration are set by the treating physician, often using a controlled infusion pump to ensure accurate delivery.

Serious risks include arrhythmias, worsening myocardial ischemia, severe hypotension, anaphylactic reactions, and hyperkalemia. Continuous cardiac monitoring during administration helps detect and manage these events promptly.

Neoton is contraindicated in patients with known hypersensitivity to phosphocreatine sodium or any excipients, and it should be avoided in individuals with uncontrolled severe arrhythmias or severe electrolyte disturbances unless closely monitored.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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