Product image of Nutriflex Omega 56/144/40 (Valine, Alanine, Arginine, Isoleucine, Leucine, Methionine, Phenylalanine, Proline, Serine, Threonin) supplied by GNH India

Nutriflex Omega 56/144/40

Active Ingredient:
Valine, Alanine, Arginine, Isoleucine, Leucine, Methionine, Phenylalanine, Proline, Serine, Threonin
Origin:
EU

Nutriflex Omega 56/144/40 (Valine, Alanine, Arginine, Isoleucine, Leucine, Methionine, Phenylalanine, Proline, Serine, Threonin)

Valine, Alanine, Arginine, Isoleucine, Leucine, Methionine, Phenylalanine, Proline, Serine, Threonine, the active ingredient in Nutriflex Omega 56/144/40, is an amino acid solution presented as an intravenous solution for intravenous use. It supplies essential and non‑essential amino acids to support protein synthesis and metabolic needs during parenteral nutrition for patients who cannot receive enteral feeding.
GNH India supplies Nutriflex Omega 56/144/40 as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

B.Braun Melsungen Ag

1
Pack/s
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Indications & Clinical Uses

Nutriflex Omega 56/144/40 is used in parenteral nutrition to provide a balanced amino acid profile for patients with compromised oral or enteral intake.

  • Patients unable to receive enteral feeding: delivers a complete set of amino acids to maintain nitrogen balance.
  • Surgical and trauma patients: supports protein synthesis and wound healing during the peri‑operative period.
  • Critically ill or intensive‑care patients: helps preserve lean body mass and metabolic stability.
  • Neonates and infants requiring parenteral nutrition: supplies essential amino acids for growth and development.

How It Works

  • The solution delivers a mixture of essential and non‑essential amino acids directly into the bloodstream, bypassing the gastrointestinal tract. These amino acids become substrates for protein synthesis, replenish intracellular pools, and support gluconeogenesis and nitrogen balance. By providing the building blocks for cellular repair and metabolic pathways, the infusion sustains organ function and promotes recovery in patients receiving parenteral nutrition.

Side Effects

Common Side Effects

  • Hyperglycemia: elevated blood glucose levels during infusion.
  • Electrolyte disturbances: shifts in potassium, sodium, or calcium.
  • Infusion site reactions: erythema, pain, or phlebitis.
  • Mild fever or chills during administration.
  • Nausea or vomiting related to metabolic changes.
  • Metabolic alkalosis: increased blood pH.

Serious or Rare Side Effects

  • Anaphylactic reaction: severe allergy requiring immediate intervention.
  • Severe hypernatremia: dangerously high sodium concentration.
  • Hepatic dysfunction: abnormal liver enzyme elevations.
  • Metabolic acidosis: low blood pH in susceptible patients.
  • Thrombophlebitis: clot formation at the catheter site.
  • Acute renal failure: sudden loss of kidney function in high‑risk individuals.

Precautions & Warnings

Nutriflex Omega 56/144/40 should be used with careful clinical monitoring.

  • Renal function: assess creatinine clearance before and during therapy.
  • Electrolyte monitoring: check serum electrolytes regularly.
  • Blood glucose: monitor glucose levels, especially in diabetic patients.
  • Compatibility: avoid mixing with calcium‑containing solutions to prevent precipitation.
  • Aseptic technique: ensure sterile handling to reduce infection risk.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Nutriflex Omega 56/144/40 may interact with other intravenous agents.

Major Interactions (Avoid)

  • Calcium‑containing solutions: risk of precipitation and catheter blockage.
  • High‑dose vitamin C: oxidative degradation of amino acids.
  • Certain antibiotics (e.g., aminoglycosides): increased nephrotoxicity.
  • Loop diuretics: amplified electrolyte shifts.
  • Parenteral lipid emulsions: potential for physical incompatibility.

Moderate Interactions (Monitor Closely)

  • Insulin therapy: may require glucose monitoring and dose adjustment.
  • Other amino‑acid solutions: cumulative amino‑acid load.
  • Anticoagulants: possible alteration of coagulation parameters.
  • Diuretics: monitor fluid and electrolyte balance.
  • Renal replacement therapy: adjust dosing based on clearance.

Frequently Asked Questions

Nutriflex Omega 56/144/40 is an intravenous amino‑acid solution used in parenteral nutrition to provide essential and non‑essential amino acids for patients who cannot receive enteral feeding, such as those in intensive care, after major surgery, or with severe trauma.

The mixture supplies the body with the building blocks needed for protein synthesis, nitrogen balance, and metabolic processes. By delivering these amino acids directly into the bloodstream, it bypasses the gastrointestinal tract and supports tissue repair, immune function, and energy metabolism.

The prescribed dose is individualized by the treating clinician based on the patient’s weight, clinical condition, renal and hepatic function, and overall nutritional goals. Dosing is calculated to meet the specific amino‑acid requirements of each patient.

Safety data in pregnancy and lactation are limited. The product should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision must be made by the prescribing physician.

Enquiries are submitted via the product page on gnhindia.com, where you specify the required quantity. GNH India supplies hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain where required) and import documentation.

Nutriflex Omega 56/144/40 offers a balanced profile of essential and non‑essential amino acids designed for comprehensive nutritional support. Compared with simpler formulations, it provides a broader spectrum of amino acids, which can better meet the metabolic demands of critically ill or surgical patients.

The solution must be stored at 2‑8 °C, protected from light, and kept in its original container. It should not be frozen or shaken. Before administration, inspect for particulate matter or discoloration and use aseptic technique.

Nutriflex Omega 56/144/40 is administered intravenously, typically via a central venous catheter or a peripheral line using an infusion pump. The infusion rate is set by the clinician according to the prescribed daily amino‑acid requirement and patient tolerance.

Serious risks include anaphylactic reactions, severe electrolyte imbalances, hypernatremia, hepatic dysfunction, metabolic acidosis, and acute renal failure. Prompt recognition and management of these events are essential, and patients should be closely monitored during therapy.

Patients with known hypersensitivity to any component of the solution, those with uncontrolled severe electrolyte disturbances, or individuals for whom compatible intravenous nutrition is contraindicated should not receive this product. Clinical judgment is required for each case.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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