Product image of Lipoflex Special, Infusionsvæske (Valine, Alanine, Arginine, Isoleucine, Leucine, Methionine, Phenylalanine, Proline, Serine, Threonin) supplied by GNH India

Lipoflex Special, Infusionsvæske

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

Lipoflex Special, Infusionsvæske (Valine, Alanine, Arginine, Isoleucine, Leucine, Methionine, Phenylalanine, Proline, Serine, Threonin)

A mixture of essential and non‑essential amino acids, the active ingredients in Lipoflex Special, Infusionsvæske, is a nutrition supplement presented as an intravenous solution for parenteral use. It provides amino acids for patients who cannot meet protein needs through oral or enteral feeding, such as those in critical care, post‑operative recovery, or with severe malnutrition.

GNH India supplies Lipoflex Special, Infusionsvæske as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and intensive care units worldwide.

Manufacturer / TM Owner

B.Braun Melsungen Ag

1
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Indications & Clinical Uses

  • Lipoflex Special, Infusionsvæske is used in parenteral nutrition to support protein synthesis and metabolic needs in patients with compromised oral intake.
  • Severe malnutrition: supplies essential amino acids to meet protein requirements when oral feeding is not possible.
  • Post‑operative recovery: aids tissue repair and nitrogen balance after major surgery.
  • Critical illness/ICU patients: provides rapid amino acid delivery for patients on mechanical ventilation or with catabolic stress.
  • Burn injuries: supports high protein turnover and wound healing in extensive burn cases.

How It Works

  • The solution delivers a balanced profile of essential and non‑essential amino acids directly into the bloodstream, bypassing gastrointestinal absorption. These amino acids become substrates for protein synthesis, replenish nitrogen stores, and support hepatic and muscular metabolic pathways, thereby maintaining lean body mass and facilitating tissue repair during periods of catabolic stress.

Side Effects

Lipoflex Special, Infusionsvæske may be associated with several adverse reactions.

Common Side Effects

  • Hyperglycemia: elevated blood glucose levels during infusion.
  • Mild infusion site irritation or erythema.
  • Electrolyte disturbances such as mild hypokalemia.
  • Nausea or transient vomiting.
  • Transient increase in serum urea.
  • Mild headache.

Serious or Rare Side Effects

  • Anaphylactic or severe allergic reaction.
  • Metabolic acidosis due to amino acid overload.
  • Severe hypernatremia or hyperosmolar states.
  • Acute renal failure in susceptible patients.
  • Thrombophlebitis at the infusion site.
  • Severe electrolyte imbalances requiring immediate intervention.

Precautions & Warnings

  • When using Lipoflex Special, Infusionsvæske, clinicians should observe several safety measures.
  • Assess renal function: adjust amino acid load in patients with impaired kidney function.
  • Monitor blood glucose: patients with diabetes may require tighter glycaemic control.
  • Check electrolytes: regular monitoring of potassium, sodium, and calcium levels is advised.
  • Avoid incompatibility: do not mix with calcium‑containing solutions to prevent precipitation.
  • Observe infusion rate: administer according to prescribed rate to reduce risk of metabolic complications.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Lipoflex Special, Infusionsvæske can interact with other intravenous agents and systemic medications.

Major Interactions (Avoid)

  • Calcium‑containing solutions: may precipitate amino acids, causing line occlusion.
  • High‑dose potassium chloride: risk of severe hyperkalemia.
  • Certain antibiotics (e.g., aminoglycosides): may increase nephrotoxicity when combined.

Moderate Interactions (Monitor Closely)

  • Concurrent glucose infusion: monitor for hyperglycemia.
  • Loop diuretics: watch electrolyte balance, especially potassium.
  • Corticosteroids: may enhance catabolic effects, requiring dosage adjustment.
  • Anticoagulants: monitor coagulation parameters as protein load can affect plasma volume.

Frequently Asked Questions

Lipoflex Special, Infusionsvæske is an intravenous amino acid solution used as part of parenteral nutrition. It supplies essential and non‑essential amino acids to patients who cannot obtain adequate protein through oral or enteral routes, such as those in intensive care, post‑surgical recovery, severe malnutrition, or extensive burns.

The amino acids in the solution are directly delivered into the bloodstream, providing immediate substrates for protein synthesis, nitrogen balance, and metabolic processes. This supports tissue repair, maintains lean body mass, and helps meet the heightened metabolic demands of critically ill or catabolic patients.

The prescribed dose is determined by the treating physician based on the patient’s weight, clinical condition, renal and hepatic function, and overall nutritional goals. Dosing is individualized and administered under medical supervision.

Safety data for use in pregnancy or lactation are limited. The product should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and this decision must be made by a qualified healthcare professional.

To place an 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.

Lipoflex Special offers a comprehensive blend of essential and non‑essential amino acids in a single sterile solution, matching or exceeding the amino acid profile of many standard parenteral formulations. Its EU‑origin manufacturing ensures compliance with GMP standards, and it is formulated for compatibility with common parenteral nutrition regimens.

The product must be stored at 2‑8 °C, protected from light, and kept in its original container. Do not freeze or shake the solution. Before use, inspect for particulate matter or discoloration and allow the bag to reach room temperature if required for infusion.

It is administered intravenously, typically via a central or peripheral line, according to the prescribing clinician’s infusion rate and volume calculations. The solution is added to the parenteral nutrition bag or infused directly, following aseptic technique and manufacturer instructions.

Serious risks include anaphylactic reactions, severe electrolyte imbalances (such as hypernatremia or hyperkalemia), metabolic acidosis, and acute renal failure in susceptible individuals. Prompt recognition and management of these events are essential, and patients should be closely monitored during infusion.

Patients with known hypersensitivity to any of the amino acids, those with severe renal or hepatic impairment without dose adjustment, and individuals receiving incompatible intravenous solutions (e.g., calcium‑containing admixtures) should not receive this product unless a risk‑benefit assessment justifies its use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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