Product image of Kidiamix G (Valine, Acetylcysteine, Alanine, Arginine, Histidine, Isoleucine, Leucine, Methionine, Phenylalanine) supplied by GNH India

Kidiamix G

Active Ingredient:
Valine, Acetylcysteine, Alanine, Arginine, Histidine, Isoleucine, Leucine, Methionine, Phenylalanine
Origin:
EU

Kidiamix G (Valine, Acetylcysteine, Alanine, Arginine, Histidine, Isoleucine, Leucine, Methionine, Phenylalanine)

Valine, Acetylcysteine, Alanine, Arginine, Histidine, Isoleucine, Leucine, Methionine, Phenylalanine, the active ingredients in Kidiamix G, are amino acids presented as a solution for injection for intravenous use. It supplies essential amino acids required for protein synthesis and metabolic functions when administered to patients who cannot receive enteral nutrition.
GNH India supplies Kidiamix G as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Fresenius Kabi Nv/Sa

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Indications & Clinical Uses

Kidiamix G is an amino acid solution used in parenteral nutrition to support patients with impaired oral or enteral intake.

  • Parenteral nutrition for patients unable to receive enteral nutrition: provides a complete profile of essential amino acids to meet protein requirements.
  • Critical illness with increased catabolism: helps maintain nitrogen balance and supports tissue repair.
  • Pre‑ and post‑operative care in major surgery: contributes to preservation of lean body mass and wound healing.

How It Works

  • Kidiamix G delivers a balanced mixture of essential amino acids directly into the bloodstream. These amino acids are taken up by cells and incorporated into nascent proteins, supporting protein synthesis, nitrogen balance, and various metabolic pathways. By bypassing the gastrointestinal tract, the solution ensures rapid availability of substrates needed for tissue repair, immune function, and metabolic homeostasis in patients receiving parenteral nutrition.

Side Effects

Kidiamix G may be associated with infusion‑related and metabolic reactions.

Common Side Effects

  • Infusion site erythema or phlebitis: mild local irritation at the catheter site.
  • Transient hypernatremia: slight increase in serum sodium during rapid infusion.
  • Mild elevation of blood urea nitrogen: reflects increased nitrogen load.
  • Temporary metabolic alkalosis: due to amino acid metabolism.

Serious or Rare Side Effects

  • Anaphylactic reaction: severe hypersensitivity requiring immediate medical intervention.
  • Severe hyperammonemia: excess ammonia accumulation, especially in hepatic impairment.
  • Septicemia from contaminated solution: rare but life‑threatening infection.
  • Significant electrolyte imbalance: may necessitate urgent correction.

Precautions & Warnings

Kidiamix G should be used with careful clinical monitoring.

  • Assess renal function: monitor creatinine and urea levels before and during therapy.
  • Monitor electrolytes: especially potassium, sodium, and calcium to avoid imbalances.
  • Adjust in hepatic impairment: watch for ammonia accumulation and consider dose modification.
  • Avoid in known hypersensitivity: discontinue if allergic reactions occur.
  • Use aseptic technique: ensure sterility of infusion set and solution.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Kidiamix G may interact with other therapies that affect nitrogen balance or electrolyte status.

Major Interactions (Avoid)

  • Concurrent high‑dose nitrogen‑producing drugs (e.g., valproic acid): may exacerbate hyperammonemia.
  • Co‑administration with other parenteral nutrition solutions containing overlapping amino acids: can lead to excess nitrogen load.

Moderate Interactions (Monitor Closely)

  • Electrolyte‑containing IV fluids: monitor for combined electrolyte shifts.
  • Renal replacement therapy: may require adjustment of amino acid infusion rate.
  • Corticosteroids or other protein‑catabolic agents: monitor overall nitrogen balance.

Frequently Asked Questions

Kidiamix G is an intravenous amino acid solution indicated for parenteral nutrition. It is used when patients cannot receive enteral feeding, such as in critical illness, major surgery, or severe gastrointestinal dysfunction, to provide essential amino acids needed for protein synthesis and metabolic maintenance.

The mixture supplies a complete set of essential amino acids that are directly absorbed into the bloodstream. Cells utilize these amino acids for protein synthesis, supporting tissue repair, immune function, and maintaining nitrogen balance, especially when oral or enteral intake is insufficient.

The dose of Kidiamix G is individualized by the prescribing clinician based on the patient’s weight, metabolic needs, renal and hepatic function, and overall nutritional goals. No fixed regimen is provided; the prescriber determines the appropriate infusion rate and total daily amount.

Safety data for Kidiamix G in pregnancy and lactation are limited. It 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 treating physician.

To order Kidiamix G, 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.

Kidiamix G offers a broad spectrum of essential amino acids in a single formulation, matching the composition recommended for adult parenteral nutrition. Compared with products that contain fewer amino acids or require multiple bags, Kidiamix G simplifies dosing and reduces the risk of amino‑acid imbalance, while meeting EU quality standards.

Kidiamix G must be stored refrigerated at 2‑8 °C. Keep the vial in its original packaging, protect it from light, and avoid freezing or shaking the solution. Before use, inspect for particulate matter or discoloration and follow aseptic techniques during preparation.

Kidiamix G is administered intravenously as an infusion. The solution is added to a compatible infusion set, diluted if required by institutional protocol, and delivered over a period determined by the prescriber, typically ranging from several hours to a continuous 24‑hour infusion, depending on the patient’s nutritional plan.

Serious risks include anaphylactic reactions, severe hyperammonemia (especially in patients with liver dysfunction), septicemia from contaminated product, and significant electrolyte disturbances. Clinicians should monitor for signs of hypersensitivity, changes in ammonia levels, and electrolyte values throughout therapy.

Kidiamix G should be avoided in individuals with known hypersensitivity to any of its amino‑acid components, in patients with uncontrolled severe electrolyte imbalances, and in those with acute hepatic failure where ammonia accumulation cannot be managed. Clinical judgment is required for each case.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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