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

Nutriflex Omega 56/144 S

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

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

Valine, Alanine, Arginine, Isoleucine, Leucine, Methionine, Phenylalanine, Proline, Serine, Threonin, the active ingredient in Nutriflex Omega 56/144 S, is an amino acid mixture presented as a parenteral nutrition solution for intravenous use. It provides essential amino acids to patients requiring nutritional support, particularly in critical care and postoperative settings.

GNH India supplies Nutriflex Omega 56/144 S as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

B.Braun Melsungen Ag

1
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Indications & Clinical Uses

Nutriflex Omega 56/144 S is used as part of parenteral nutrition regimens for patients who cannot meet protein and amino‑acid requirements orally.

  • Critical illness: supports protein synthesis and nitrogen balance in intensive‑care patients.
  • Post‑operative recovery: aids wound healing and tissue repair after major surgery.
  • Severe malnutrition: supplies essential amino acids when oral intake is insufficient or contraindicated.

How It Works

  • The formulation delivers a balanced profile of essential and non‑essential amino acids directly into the bloodstream, bypassing gastrointestinal absorption. These amino acids serve as substrates for protein synthesis, support nitrogen balance, and act as precursors for neurotransmitters and metabolic intermediates, thereby sustaining cellular function during periods of catabolic stress.

Side Effects

Adverse reactions are generally related to the intravenous route and the amino‑acid composition.

Common Side Effects

  • Mild infusion site erythema: localized redness at the catheter site.
  • Transient nausea: brief episodes of nausea during or shortly after infusion.
  • Hyperglycaemia: temporary rise in blood glucose levels, especially in diabetic patients.
  • Electrolyte shifts: mild changes in serum potassium or phosphate.
  • Headache: occasional mild headache during treatment.

Serious or Rare Side Effects

  • Anaphylactic reaction: severe allergic response requiring immediate medical intervention.
  • Severe hyperammonemia: marked increase in blood ammonia levels.
  • Metabolic acidosis: significant drop in blood pH.
  • Hepatic dysfunction: abnormal liver enzyme elevations.
  • Renal impairment: worsening kidney function in susceptible individuals.

Precautions & Warnings

When prescribing Nutriflex Omega 56/144 S, clinicians should consider patient‑specific factors and monitor relevant parameters.

  • Renal function: assess creatinine clearance before initiation and during therapy.
  • Hepatic status: evaluate liver enzymes and function tests.
  • Metabolic disorders: monitor glucose and electrolyte levels regularly.
  • Allergic history: verify absence of known hypersensitivity to any amino‑acid component.
  • Infusion rate: adhere to recommended infusion speeds to minimise phlebitis.
  • Store at 2‑8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Amino‑acid solutions may interact with certain medications or clinical conditions.

Major Interactions (Avoid)

  • High‑dose potassium supplements: can exacerbate hyperkalaemia when combined.
  • Certain antibiotics (e.g., aminoglycosides): may increase nephrotoxic risk.

Moderate Interactions (Monitor Closely)

  • Insulin therapy: may require dose adjustment due to glucose fluctuations.
  • Loop diuretics: monitor electrolyte balance, especially potassium and magnesium.
  • Anticonvulsants (e.g., valproate): may alter plasma amino‑acid levels.
  • Corticosteroids: can affect protein catabolism rates.
  • Total parenteral nutrition admixtures: ensure compatibility before co‑administration.

Frequently Asked Questions

Nutriflex Omega 56/144 S is an intravenous amino‑acid mixture used as part of total parenteral nutrition to provide essential proteins for patients who cannot obtain adequate nutrition by mouth, such as those in intensive care, after major surgery, or with severe malnutrition.

The solution delivers a balanced blend of essential and non‑essential amino acids directly into the bloodstream, supplying the building blocks for protein synthesis, supporting nitrogen balance, and providing precursors for metabolic pathways that maintain cellular function during catabolic stress.

The prescribed dose of Nutriflex Omega 56/144 S is individualized by the treating clinician based on the patient’s weight, metabolic needs, renal and hepatic function, and overall nutritional goals. Exact dosing regimens are determined in a clinical setting.

Safety data for Nutriflex Omega 56/144 S in pregnancy and lactation are limited. It should only be used when clearly indicated and when the potential benefits outweigh any potential risks, under close medical supervision.

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.

Nutriflex Omega 56/144 S offers a comprehensive profile of ten amino acids designed for balanced protein provision, similar to other commercial amino‑acid admixtures. Differences may lie in individual amino‑acid concentrations, osmolarity, and compatibility with other total parenteral nutrition components, which clinicians evaluate when selecting a product.

The product must be stored refrigerated at 2‑8 °C, protected from light, and should not be frozen or shaken. Prior to use, inspect the container for any particulate matter or discoloration and allow the solution to reach room temperature if required by the administration protocol.

Nutriflex Omega 56/144 S is administered intravenously, typically as an infusion added to a total parenteral nutrition regimen. The infusion rate is set according to the prescribing clinician’s orders, and the solution is delivered through a dedicated line or compatible Y‑site, following aseptic technique.

Serious risks include anaphylactic reactions, severe hyperammonemia, metabolic acidosis, hepatic dysfunction, and renal impairment. Prompt recognition of these events and immediate medical intervention are essential to mitigate harm.

Patients with known hypersensitivity to any component of the amino‑acid mixture, those with uncontrolled hyperammonemia, severe hepatic failure, or uncontrolled electrolyte disturbances should not receive Nutriflex Omega 56/144 S unless benefits clearly outweigh risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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