Product image of Olimel Perifer N4e (Valine, Alanine, Arginine, Histidine, Isoleucine, Leucine, Methionine, Phenylalanine, Proline, Serin) supplied by GNH India

Olimel Perifer N4e

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

Olimel Perifer N4e (Valine, Alanine, Arginine, Histidine, Isoleucine, Leucine, Methionine, Phenylalanine, Proline, Serin)

Valine, Alanine, Arginine, Histidine, Isoleucine, Leucine, Methionine, Phenylalanine, Proline, Serin, the active ingredient in Olimel Perifer N4e, is a mixture of essential and non‑essential amino acids presented as a sterile powder for intravenous use. It supports metabolic processes and protein synthesis in patients requiring nutritional supplementation.

GNH India supplies Olimel Perifer N4e as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and transplant centres worldwide.

Manufacturer / TM Owner

Baxter Medical Ab

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Indications & Clinical Uses

Olimel Perifer N4e provides amino acid supplementation for conditions that increase protein catabolism. It is used in clinical settings to support:

  • Post‑operative recovery: helps maintain nitrogen balance during the healing phase.
  • Severe trauma or burns: supplies essential amino acids to support tissue repair.
  • Long‑term parenteral nutrition: provides a balanced amino acid profile for patients unable to receive enteral feeding.

How It Works

  • The formulation delivers a balanced mixture of essential and non‑essential amino acids directly into the bloodstream, bypassing gastrointestinal absorption. These amino acids serve as substrates for protein synthesis, support gluconeogenesis, and contribute to the synthesis of neurotransmitters and immune mediators, thereby aiding recovery in catabolic states.

Side Effects

Amino acid solutions are generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Mild nausea or vomiting: transient gastrointestinal discomfort.
  • Transient hyperglycaemia: elevation of blood glucose that resolves with monitoring.
  • Local irritation at the infusion site: redness or mild pain.
  • Headache: mild, self‑limiting.
  • Electrolyte shifts: mild changes in serum potassium or calcium.
  • Fever: low‑grade temperature rise during infusion.

Serious or Rare Side Effects

  • Anaphylactic reaction: sudden onset of urticaria, bronchospasm, or hypotension.
  • Severe hyperosmolarity: rapid infusion may cause osmotic imbalance.
  • Metabolic acidosis: rare but possible with prolonged high‑dose use.
  • Thrombophlebitis: inflammation of the vein with clot formation.
  • Renal dysfunction: acute changes in kidney function in susceptible patients.
  • Sepsis: contamination‑related infection, though extremely rare with aseptic preparation.

Precautions & Warnings

When prescribing Olimel Perifer N4e, clinicians should consider patient‑specific factors and monitor relevant parameters.

  • Assess renal function: adjust infusion rate in patients with impaired clearance.
  • Monitor blood glucose: amino acids can affect glycaemic control, especially in diabetics.
  • Check electrolyte balance: watch for shifts in potassium, calcium, and phosphate.
  • Observe for infusion reactions: be prepared to manage hypersensitivity.
  • Use aseptic technique: maintain sterility throughout preparation and administration.
  • Store at ambient temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Amino acid solutions may interact with certain medications or clinical conditions.

Major Interactions (Avoid)

  • High‑dose insulin therapy: may exacerbate hypoglycaemia when combined with amino acid‑induced glucose shifts.
  • Potassium‑sparing diuretics: increase risk of hyperkalaemia when large amino acid loads are infused.

Moderate Interactions (Monitor Closely)

  • Anticoagulants (e.g., heparin): monitor coagulation parameters as amino acids can affect plasma protein binding.
  • Corticosteroids: may increase protein catabolism, requiring adjustment of amino acid dosing.
  • Loop diuretics: monitor electrolytes closely due to combined effects on renal excretion.
  • Beta‑blockers: may mask tachycardia that can signal infusion reactions.
  • Parenteral lipid emulsions: coordinate infusion timing to avoid incompatibility.

Frequently Asked Questions

Olimel Perifer N4e is an intravenous amino acid solution used to provide balanced protein building blocks for patients who cannot receive normal oral or enteral nutrition, such as those recovering from surgery, severe trauma, burns, or who are on long‑term parenteral nutrition.

The mixture supplies essential and non‑essential amino acids directly into the bloodstream, bypassing the gut. These amino acids act as substrates for protein synthesis, support gluconeogenesis, and help maintain nitrogen balance, which is critical during catabolic stress.

The prescribed dose is individualized by the treating clinician based on the patient’s weight, metabolic needs, and clinical condition. Dosing calculations are performed by the healthcare team and are not standardized across all patients.

Safety data for this intravenous amino acid formulation in pregnancy or 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 under close medical supervision.

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 and any necessary import documentation.

Olimel Perifer N4e offers a comprehensive blend of ten amino acids in a sterile powder form, providing a balanced profile for metabolic support. Compared with single‑amino‑acid solutions, it reduces the need for multiple products and simplifies formulation of parenteral nutrition regimens.

The product should be stored at ambient temperature, below 25 °C, in its original packaging. It must be protected from moisture and direct sunlight. Reconstitute only with sterile diluent immediately before use, following aseptic technique.

The sterile powder is reconstituted with a compatible sterile diluent and infused intravenously under aseptic conditions. Administration rate and duration are determined by the prescribing clinician, typically using infusion pumps to ensure controlled delivery.

Serious risks include anaphylactic reactions, severe hyperosmolarity, metabolic acidosis, thrombophlebitis, renal dysfunction and, rarely, infection from contaminated solutions. Prompt recognition and management of these events are essential.

Patients with known hypersensitivity to any component of the formulation, uncontrolled hyperkalaemia, severe renal impairment without dose adjustment, or those at high risk for anaphylaxis should not receive this product unless benefits clearly outweigh risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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