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 supports protein synthesis and provides essential amino acids for patients unable to receive enteral feeding.

GNH India supplies Kidiamix G as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Fresenius Kabi Nederland B.V.

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Indications & Clinical Uses

Kidiamix G is used in the context of parenteral nutrition to address protein and amino‑acid needs in patients who cannot be fed enterally.

  • Parenteral nutrition: provides essential amino acids for patients who cannot receive enteral feeding.
  • Critical illness support: assists protein synthesis and nitrogen balance in ICU patients.
  • Post‑operative care: helps prevent amino‑acid deficiency after major surgery.

How It Works

  • Kidiamix G delivers a balanced mixture of essential and non‑essential amino acids directly into the bloodstream. These amino acids serve as substrates for ribosomal protein synthesis, replenish nitrogen stores, and act as precursors for neurotransmitters, hormones, and metabolic intermediates, thereby supporting cellular growth and repair when oral intake is not possible.

Side Effects

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

Common Side Effects

  • Phlebitis at the infusion site
  • Mild fever or chills
  • Nausea or vomiting
  • Headache
  • Transient hyperglycemia
  • Electrolyte shifts (e.g., mild hypokalemia)

Serious or Rare Side Effects

  • Anaphylactic reaction
  • Severe hypotension
  • Metabolic acidosis
  • Hepatic dysfunction
  • Acute renal failure
  • Severe electrolyte disturbances (e.g., hypernatremia)

Precautions & Warnings

Kidiamix G requires careful monitoring in several clinical situations.

  • Renal impairment: monitor renal function and adjust infusion rate.
  • Hepatic dysfunction: use with caution; assess liver enzymes.
  • Electrolyte balance: regularly check serum electrolytes.
  • Metabolic disorders: evaluate nitrogen balance and acid‑base status.
  • Hypersensitivity: discontinue if signs of allergic reaction appear.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Kidiamix G can interact with other therapies that affect amino‑acid or electrolyte homeostasis.

Major Interactions (Avoid)

  • Concurrent high‑dose amino‑acid solutions: risk of overload and metabolic imbalance.
  • Renal replacement therapy: may remove administered amino acids, reducing efficacy.
  • Insulin therapy: may potentiate hypoglycemia when combined with glucose‑containing solutions.

Moderate Interactions (Monitor Closely)

  • Electrolyte‑containing medications: monitor serum levels for additive effects.
  • Diuretics: may exacerbate electrolyte loss.
  • Certain chemotherapeutic agents: may alter protein metabolism and require dose adjustment.

Frequently Asked Questions

Kidiamix G is an intravenous amino‑acid solution used as part of parenteral nutrition. It provides essential and non‑essential amino acids to patients who cannot receive nutrition through the gastrointestinal tract, such as those in intensive care, post‑surgical settings, or with severe malabsorption.

The mixture supplies the building blocks required for protein synthesis, supports nitrogen balance, and serves as precursors for metabolic pathways. By delivering these amino acids directly into the bloodstream, it bypasses the need for intestinal absorption and helps maintain cellular function during periods of catabolic stress.

The dose of Kidiamix G is individualized by the prescribing clinician based on the patient’s weight, clinical condition, renal and hepatic function, and overall nutritional goals. Healthcare professionals calculate the infusion rate and total daily amount to meet specific protein and caloric requirements.

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 a qualified healthcare provider.

To place an order, submit an enquiry on the product page at gnhindia.com with 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 comprehensive blend of essential and non‑essential amino acids in a single sterile solution, which can simplify formulation compared with multi‑component kits. Its EU‑origin manufacturing ensures compliance with GMP standards, while alternative products may vary in amino‑acid composition, concentration, or regulatory status.

Kidiamix G must be stored refrigerated at 2‑8 °C, protected from light, and should never be frozen or vigorously shaken. Before use, inspect the vial for particulate matter or discoloration and allow it to reach room temperature if required by the administration protocol.

Kidiamix G is administered intravenously as a sterile solution for injection. It is typically infused through a dedicated line or a compatible infusion set, following aseptic technique. The infusion rate is set by the clinician according to the prescribed dosage and patient tolerance.

Serious risks include anaphylactic reactions, severe hypotension, metabolic acidosis, hepatic dysfunction, acute renal failure, and profound electrolyte disturbances. Prompt recognition and management of these events are essential, and patients should be monitored closely during and after infusion.

Kidiamix G is contraindicated in patients with known hypersensitivity to any of its amino‑acid components, those with uncontrolled severe metabolic disorders, or individuals for whom intravenous amino‑acid administration is medically inappropriate. Clinical judgment should guide exclusion in cases of severe organ dysfunction.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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