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

Nephrosteril

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

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

Valine, the active ingredient in Nephrosteril, is an amino‑acid component formulated as an intravenous solution for infusion use. The product also contains acetylcysteine, alanine, arginine, histidine, isoleucine, leucine, methionine and phenylalanine, providing a balanced amino‑acid profile that may be employed in clinical research or supportive care settings. GNH India supplies Nephrosteril as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. The company adheres to EU manufacturing standards and provides regulatory documentation for global distribution.

Manufacturer / TM Owner

Fresenius Kabi Deutschland Gmbh

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Indications & Clinical Uses

  • Nephrosteril is an intravenous amino‑acid blend that has been explored in supportive care and metabolic research.
  • Investigational metabolic support: supplies essential amino acids for study of metabolic disorders.
  • Renal support research: evaluated as adjunct in renal replacement therapy protocols.
  • Nutritional supplementation in critical care: used to assess impact on protein synthesis.

How It Works

  • Nephrosteril delivers a mixture of essential and non‑essential amino acids directly into the bloodstream, bypassing gastrointestinal absorption. The amino acids serve as substrates for protein synthesis, act as precursors for glutathione via cysteine, and may modulate oxidative‑stress pathways. By raising plasma amino‑acid concentrations, the formulation can support cellular metabolism, immune function, and tissue repair in settings where endogenous supplies are limited.

Side Effects

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

Common Side Effects

  • Phlebitis at the infusion site
  • Mild nausea or vomiting
  • Transient headache
  • Slight elevation of body temperature
  • Mild hypotension during infusion
  • Temporary electrolyte shift (e.g., mild hyperkalemia)

Serious or Rare Side Effects

  • Anaphylactic or severe hypersensitivity reaction
  • Acute renal failure in susceptible patients
  • Severe electrolyte imbalance (e.g., hypernatremia, severe hyperkalemia)
  • Cardiac arrhythmia linked to electrolyte disturbances
  • Severe metabolic acidosis
  • Pulmonary edema from fluid overload

Precautions & Warnings

  • When using Nephrosteril, clinicians should observe several safety measures.
  • Assess renal function: evaluate baseline creatinine and glomerular filtration rate.
  • Monitor electrolytes: check serum levels before and during infusion.
  • Observe for infusion reactions: watch for rash, itching, or respiratory distress.
  • Avoid in known hypersensitivity: discontinue immediately if severe allergic response occurs.
  • Pregnancy and lactation: use only if potential benefit justifies potential risk.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Nephrosteril can interact with other medications and therapies.

Major Interactions (Avoid)

  • Concurrent high‑dose glutathione precursors: risk of metabolic overload.
  • Renal replacement therapy circuits: may alter clearance of amino acids.
  • Anticoagulants (e.g., heparin): potential additive bleeding risk.

Moderate Interactions (Monitor Closely)

  • Loop diuretics: monitor electrolytes for additive shifts.
  • Insulin therapy: amino‑acid load may affect glucose metabolism.
  • Other intravenous amino‑acid solutions: risk of excess amino‑acid load.

Frequently Asked Questions

Nephrosteril is an intravenous formulation that provides a blend of essential and non‑essential amino acids. It is primarily used in clinical research and supportive care settings to evaluate the effects of amino‑acid supplementation on metabolism, nutrition, and organ function.

Valine, one of the branched‑chain amino acids in Nephrosteril, serves as a substrate for protein synthesis and can influence muscle metabolism. Together with the other amino acids, it helps raise plasma amino‑acid levels, supporting cellular repair and metabolic pathways.

The dosage of Nephrosteril is determined by the prescribing clinician based on the specific study protocol or therapeutic objective. Dosing is individualized and should follow the guidance of a qualified healthcare professional.

Safety data for Nephrosteril in pregnancy or 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 under close medical supervision.

To order Nephrosteril, 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.

Nephrosteril offers a comprehensive blend of nine amino acids, whereas many alternative products contain a more limited set. This broader profile may provide a more balanced substrate for protein synthesis and metabolic support, but comparative efficacy depends on the clinical context and study design.

Nephrosteril should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the product from direct sunlight, moisture, and extreme temperature fluctuations to maintain stability.

Nephrosteril is administered intravenously by a qualified healthcare professional. The solution is typically infused over a prescribed period using aseptic technique, with monitoring for any infusion‑related reactions.

Serious risks include severe hypersensitivity reactions such as anaphylaxis, acute renal failure in vulnerable patients, significant electrolyte disturbances that can lead to cardiac arrhythmias, and metabolic acidosis. Prompt recognition and management of these events are essential.

Nephrosteril 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 where the risk of fluid overload outweighs potential benefits. Clinical judgment is required for each case.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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