Product image of Numeta G13e (Valine, Ornithine Hydrochloride, Alanine, Arginine, Cysteine, Histidine, Isoleucine, Leucine, Methio) supplied by GNH India

Numeta G13e

Active Ingredient:
Valine, Ornithine Hydrochloride, Alanine, Arginine, Cysteine, Histidine, Isoleucine, Leucine, Methio
Origin:
EU

Numeta G13e (Valine, Ornithine Hydrochloride, Alanine, Arginine, Cysteine, Histidine, Isoleucine, Leucine, Methio)

A mixture of essential and non‑essential amino acids, the active ingredient in Numeta G13e, is an amino acid solution presented as a parenteral formulation for intravenous use. It supplies balanced amino acid nutrition to patients who cannot receive enteral feeding, such as critically ill, postoperative or neonatal patients.

GNH India supplies Numeta G13e as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable logistics for global distribution.

Manufacturer / TM Owner

Baxter Oy

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Indications & Clinical Uses

  • Numeta G13e is used in parenteral nutrition to provide essential amino acids for patients unable to receive oral or enteral feeding.
  • Critical illness: supports protein synthesis and nitrogen balance in critically ill patients.
  • Post‑operative care: aids recovery by supplying amino acids after major surgery.
  • Neonatal nutrition: provides balanced amino acid profile for preterm or low‑birth‑weight infants.
  • Renal or hepatic impairment: offers tailored amino acid composition for patients with organ dysfunction.

How It Works

  • Numeta G13e delivers a balanced mixture of essential and non‑essential amino acids directly into the bloodstream. The amino acids are taken up by cells via specific transporters, serving as substrates for protein synthesis, gluconeogenesis and energy production. By supplying nitrogen and carbon skeletons, the solution helps restore the body’s amino acid pool, supporting tissue repair, immune function and metabolic homeostasis during periods of catabolic stress.

Side Effects

Intravenous amino acid solutions may be associated with a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Hyperglycaemia: elevated blood glucose levels, especially in diabetic patients.
  • Electrolyte disturbances: shifts in potassium, phosphate or magnesium.
  • Mild infusion site reactions: erythema, warmth or discomfort at the catheter site.
  • Increased serum urea: transient rise due to amino acid catabolism.
  • Fluid overload: signs of edema or pulmonary congestion in volume‑sensitive patients.

Serious or Rare Side Effects

  • Allergic reaction: urticaria, bronchospasm or anaphylaxis requiring immediate treatment.
  • Metabolic acidosis: significant drop in blood pH due to excess amino acid metabolism.
  • Hepatic dysfunction: abnormal liver enzymes in patients with pre‑existing liver disease.
  • Hyperammonemia: elevated ammonia levels, particularly in severe liver impairment.

Precautions & Warnings

When prescribing Numeta G13e, clinicians should observe several precautionary measures to ensure safe administration.

  • Patient assessment: evaluate renal, hepatic and metabolic status before initiation.
  • Monitoring: regularly check blood glucose, electrolytes and nitrogen balance during therapy.
  • Infusion rate: administer according to recommended speed to avoid circulatory overload.
  • Compatibility: verify compatibility with other intravenous solutions and medications.
  • Pregnancy and lactation: use only if benefits outweigh potential risks; limited data available.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Amino acid solutions can interact with certain drugs and clinical conditions, necessitating awareness of potential interactions.

Major Interactions (Avoid)

  • High‑dose insulin: concurrent use may cause severe hypoglycaemia.
  • Loop diuretics: may exacerbate electrolyte imbalances, especially potassium loss.
  • Acidifying agents: can increase risk of metabolic acidosis when combined.

Moderate Interactions (Monitor Closely)

  • Corticosteroids: may increase protein catabolism, requiring dosage adjustment.
  • Anticonvulsants (e.g., phenobarbital): may alter amino acid metabolism.
  • Renal replacement therapy: may necessitate modified dosing or monitoring.
  • Parenteral lipid emulsions: co‑administration requires careful monitoring of caloric load.

Frequently Asked Questions

Numeta G13e is a parenteral amino acid solution designed to provide balanced protein precursors to patients who cannot receive oral or enteral nutrition. It is commonly employed in intensive care, postoperative recovery, neonatal intensive care, and in individuals with renal or hepatic impairment who require intravenous nutritional support.

The formulation contains a blend of essential and non‑essential amino acids that are rapidly absorbed into the bloodstream. Cells take up these amino acids via specific transporters, using them for protein synthesis, gluconeogenesis, and energy production, thereby replenishing the body’s amino acid pool during catabolic stress.

The dosage of Numeta G13e is individualized and set by the prescribing clinician based on the patient’s weight, metabolic needs, and clinical condition. Dosing calculations follow established parenteral nutrition guidelines and are adjusted according to laboratory monitoring and therapeutic response.

Data on the use of Numeta G13e 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 should be made by the treating physician in consultation with obstetric specialists.

To request Numeta G13e, 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 the necessary import documentation.

Numeta G13e offers a comprehensive profile of both essential and non‑essential amino acids, meeting European pharmacopeial standards for parenteral nutrition. Compared with older formulations, it provides a more balanced nitrogen load and improved solubility, which can reduce the risk of precipitation when mixed with other intravenous components.

Numeta G13e must be stored refrigerated at 2‑8 °C. Keep the container in its original packaging, protect it from direct light, and avoid freezing or shaking. Before use, inspect the solution for any particles or discoloration and discard if integrity is compromised.

The product is administered intravenously, typically diluted in a compatible carrier solution. Infusion rates are determined by the prescribing clinician and should follow institutional protocols to avoid fluid overload. Continuous monitoring of vital signs and laboratory parameters is recommended throughout the infusion.

Serious adverse events include hypersensitivity reactions such as anaphylaxis, metabolic acidosis, and hyperammonemia, especially in patients with severe liver dysfunction. Prompt recognition and management of these conditions are essential, and clinicians should monitor relevant laboratory values during therapy.

Numeta G13e is contraindicated in individuals with known hypersensitivity to any of its amino acid components. It should also be avoided in patients with uncontrolled severe hepatic failure, severe metabolic disorders, or those at high risk for fluid overload unless close monitoring and dose adjustments are feasible.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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