Product image of Junyelt (Copper Gluconate, Manganese Gluconate, Potassium Iodide, Sodium Selenite, Zinc Gluconate) supplied by GNH India

Junyelt

Active Ingredient:
Copper Gluconate, Manganese Gluconate, Potassium Iodide, Sodium Selenite, Zinc Gluconate
Origin:
EU

Junyelt (Copper Gluconate, Manganese Gluconate, Potassium Iodide, Sodium Selenite, Zinc Gluconate)

Copper gluconate, manganese gluconate, potassium iodide, sodium selenite, zinc gluconate, the active ingredients in Junyelt, are trace element supplements presented as a sterile solution for injection for intravenous use. They are employed to correct or prevent micronutrient deficiencies in patients receiving parenteral nutrition or who have increased metabolic demands.

GNH India supplies Junyelt as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. The product is manufactured in the European Union under strict quality standards.

Manufacturer / TM Owner

Laboratoire Aguettant

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Indications & Clinical Uses

  • Junyelt is a trace element supplement used in clinical settings that require parenteral provision of essential micronutrients.
  • Micronutrient deficiency: restores copper, manganese, iodine, selenium, and zinc levels in patients with documented deficiencies.
  • Parenteral nutrition: supplies essential trace elements as part of total parenteral nutrition admixtures for patients unable to take oral nutrition.
  • Pre‑operative preparation: optimizes trace element status before major surgery to support metabolic and immune function.

How It Works

  • The constituents of Junyelt act as essential cofactors for a variety of enzymatic reactions. Intravenous administration bypasses gastrointestinal absorption, delivering copper, manganese, iodine, selenium, and zinc directly into the bloodstream where they are incorporated into metalloenzymes, antioxidant selenoproteins, thyroid hormone synthesis pathways, and other cellular processes critical for oxidative defense, energy production, and immune competence. These trace elements support the activity of enzymes such as cytochrome c oxidase, superoxide dismutase, and deiodinases, thereby influencing metabolic and endocrine functions.

Side Effects

Junyelt may be associated with the following adverse reactions, which vary in frequency and severity.

Common Side Effects

  • Injection site pain: mild discomfort at the infusion site.
  • Transient metallic taste: brief metallic sensation in the mouth.
  • Nausea: mild upset stomach following administration.
  • Headache: mild to moderate headache occurring shortly after infusion.

Serious or Rare Side Effects

  • Anaphylactic reaction: severe allergic response requiring immediate medical intervention.
  • Copper or selenium toxicity: signs of excess such as abdominal pain, vomiting, or neurological symptoms.

Precautions & Warnings

When using Junyelt, clinicians should observe the following precautions to ensure safe administration.

  • Baseline assessment: evaluate serum trace element levels before initiating therapy.
  • Therapeutic monitoring: regularly measure copper, manganese, iodine, selenium, and zinc concentrations during treatment.
  • Hypersensitivity: avoid in patients with known allergy to any component of the formulation.
  • Organ impairment: use with caution in patients with severe renal or hepatic dysfunction.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Junyelt can interact with other medicines; awareness of these interactions helps prevent adverse outcomes.

Major Interactions (Avoid)

  • High‑dose copper supplements: may cause copper overload and toxicity.
  • High‑dose selenium supplements: increase risk of selenosis.
  • Iodine‑containing contrast agents: can alter thyroid function when combined.

Moderate Interactions (Monitor Closely)

  • Anticoagulants: trace elements may affect platelet function and alter bleeding risk.
  • Thyroid hormone therapy: iodine content may require adjustment of levothyroxine dose.
  • Renal dialysis: procedure may remove administered trace elements, reducing efficacy.

Frequently Asked Questions

Junyelt is an intravenous trace element supplement that provides copper, manganese, iodine, selenium and zinc. It is used to correct or prevent micronutrient deficiencies in patients receiving total parenteral nutrition, those with increased metabolic demands, or individuals at risk of trace‑element depletion.

The five trace elements in Junyelt serve as essential cofactors for enzymes involved in oxidative defence, thyroid hormone synthesis, and cellular metabolism. Delivered directly into the bloodstream, they bypass gastrointestinal absorption and become incorporated into metallo‑enzymes, selenoproteins and other biochemical pathways that support immune function and energy production.

The dose of Junyelt is individualized by the prescribing clinician based on the patient’s laboratory‑determined trace‑element status, clinical condition, and the composition of the overall parenteral nutrition regimen. No fixed regimen is provided in public literature; the prescriber sets the appropriate volume and frequency.

Safety data for Junyelt in pregnancy and lactation are limited. Because copper, iodine and selenium can affect fetal development and thyroid function, the product should only be used when the potential benefit justifies any possible risk. The prescriber should evaluate the maternal‑fetal risk‑benefit profile before administration.

To request Junyelt, submit an enquiry on the product page at gnhindia.com indicating the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain handling if required) and the necessary import documentation.

Junyelt combines five essential trace elements in a single sterile solution, whereas many alternatives provide only one or two elements per vial. This multi‑element formulation can simplify compounding for total parenteral nutrition and reduce the number of separate injections, but clinicians should still monitor individual element levels to avoid excess.

Junyelt must be stored at 2‑8 °C in a refrigerator, protected from light. The container should not be frozen or shaken. Before use, inspect the solution for particulate matter or discoloration and allow it to reach room temperature if required by the infusion protocol.

Junyelt is administered intravenously, typically added to a compatible parenteral nutrition bag or infused as a separate line according to the prescriber’s instructions. The infusion rate and total volume are determined by the patient’s clinical needs and the overall nutrition plan.

The most serious risks include anaphylactic or severe hypersensitivity reactions and toxicity from excess copper or selenium, which can present with abdominal pain, vomiting, neurological changes, or hepatic dysfunction. Prompt recognition and medical management are essential if these events occur.

Junyelt should be avoided in patients with known hypersensitivity to any of its components, in those with documented copper or selenium overload, and in individuals with severe uncontrolled renal or hepatic failure where trace‑element clearance is markedly impaired.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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