Product image of Kabiven (Valine, Alanine, Arginine, Histidine, Isoleucine, Leucine, Methionine, Phenylalanine, Proline, Serin) supplied by GNH India

Kabiven

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

Kabiven (Valine, Alanine, Arginine, Histidine, Isoleucine, Leucine, Methionine, Phenylalanine, Proline, Serin)

Valine, Alanine, Arginine, Histidine, Isoleucine, Leucine, Methionine, Phenylalanine, Proline, Serine, the active ingredient in Kabiven, is an amino acid solution presented as a solution for injection for intravenous use. It supplies essential amino acids to support protein synthesis, maintain nitrogen balance, and provide nutritional support for patients who cannot receive enteral feeding, such as postoperative or critically ill individuals.

GNH India supplies Kabiven as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Fresenius Kabi Limited

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Indications & Clinical Uses

Kabiven is used to provide amino acid supplementation for patients receiving parenteral nutrition.

  • Parenteral nutrition: supports protein synthesis and nitrogen balance in patients unable to receive enteral feeding.
  • Post‑operative care: supplies essential amino acids to promote recovery after surgery.
  • Critical care: maintains nutritional status in intensive‑care patients with high metabolic demand.

How It Works

  • Kabiven delivers a balanced mixture of essential and non‑essential amino acids directly into the bloodstream. These amino acids are taken up by cells and incorporated into new proteins, supporting tissue repair, immune function, and the maintenance of nitrogen balance. By bypassing the gastrointestinal tract, the solution ensures rapid availability of substrates for protein synthesis in patients who cannot tolerate oral or enteral nutrition.

Side Effects

Kabiven may be associated with several adverse reactions during or after infusion.

Common Side Effects

  • Hyperglycemia: elevated blood glucose levels, especially in diabetic patients.
  • Electrolyte disturbances: changes in potassium, sodium, or calcium concentrations.
  • Infusion site reactions: erythema, pain, or phlebitis at the catheter site.
  • Nausea or vomiting: gastrointestinal discomfort during administration.
  • Mild metabolic alkalosis: slight increase in blood pH.
  • Increased blood urea nitrogen: reflecting nitrogen load.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction with respiratory distress.
  • Severe hypernatremia: dangerously high sodium levels.
  • Severe metabolic acidosis: significant drop in blood pH.
  • Hepatic dysfunction: abnormal liver enzyme elevations.
  • Renal failure: worsening kidney function in susceptible patients.
  • Thrombophlebitis: clot formation with vein inflammation.

Precautions & Warnings

When using Kabiven, clinicians should observe several safety measures.

  • Monitor blood glucose: check levels regularly, especially in diabetic patients.
  • Monitor electrolytes: assess serum potassium, sodium, calcium, and magnesium.
  • Adjust dose in renal or hepatic impairment: reduce infusion rate as needed.
  • Use aseptic technique: prevent contamination during preparation and administration.
  • Avoid in patients with known hypersensitivity to any component of the solution.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Kabiven can interact with other medications that affect electrolyte balance or nitrogen load.

Major Interactions (Avoid)

  • Concurrent high‑dose potassium chloride: risk of severe hyperkalemia.
  • Co‑administration with other amino acid solutions: may cause excess nitrogen burden.
  • Use with certain diuretics (e.g., loop diuretics) without electrolyte monitoring: can precipitate electrolyte shifts.

Moderate Interactions (Monitor Closely)

  • Insulin therapy: may require glucose monitoring due to potential hyperglycemia.
  • Corticosteroids: can alter protein catabolism and affect nutritional needs.
  • Nephrotoxic drugs (e.g., aminoglycosides): monitor renal function closely.

Frequently Asked Questions

Kabiven 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 postoperative recovery, intensive‑care units, or with severe malabsorption.

The mixture supplies the building blocks required for protein synthesis directly into the bloodstream. Cells uptake these amino acids to repair tissue, support immune function, and maintain nitrogen balance, thereby meeting the metabolic needs of patients who are unable to ingest food orally or enterally.

The dose of Kabiven is individualized by the prescribing clinician based on the patient’s weight, clinical condition, renal and hepatic function, and overall nutritional goals. No fixed regimen is provided; the healthcare professional determines the appropriate infusion rate and volume.

Safety data for Kabiven in pregnancy and lactation are limited. It should only be used when 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 Kabiven, 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 any required import documentation.

Kabiven offers a balanced profile of essential and non‑essential amino acids comparable to other commercial parenteral amino acid formulations. Differences may lie in individual amino‑acid concentrations, osmolarity, and compatibility with other intravenous components, which clinicians consider when selecting the most suitable product for a specific patient.

Kabiven must be stored refrigerated at 2‑8 °C, protected from light, and should never be frozen or shaken. Keep the container in its original packaging until use and discard any solution that appears discolored or contains particles.

Kabiven is administered intravenously, typically via a central or peripheral venous catheter. The solution is infused over a period determined by the prescribing clinician, using aseptic technique and appropriate infusion equipment to ensure safe delivery.

Serious risks include anaphylactic reactions, severe electrolyte disturbances such as hypernatremia or hyperkalemia, metabolic acidosis or alkalosis, hepatic dysfunction, and renal failure. Prompt recognition and management of these events are essential.

Kabiven should be avoided in patients with known hypersensitivity to any of its amino‑acid components, in those with severe uncontrolled renal or hepatic failure, and in individuals where the risk of fluid overload or electrolyte imbalance outweighs the nutritional benefit.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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