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, and zinc gluconate, the active ingredients in Junyelt, are a mineral supplement presented as an intravenous solution for parenteral administration. They are used to correct trace element deficiencies, support metabolic processes, and aid recovery in patients receiving intravenous nutrition or who have increased mineral loss.
GNH India supplies Junyelt as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Laboratoire Aguettant

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Indications & Clinical Uses

Junyelt, a parenteral mineral supplement, is used to correct trace element deficiencies and support metabolic processes in clinical nutrition.

  • Micronutrient deficiency: Restores copper, manganese, iodine, selenium, and zinc levels in patients with documented deficiencies.
  • Total parenteral nutrition (TPN): Provides essential trace elements as part of comprehensive intravenous nutrition regimens.
  • Post‑operative recovery: Supports wound healing and immune function by supplying key minerals after major surgery.

How It Works

  • After intravenous infusion, the gluconate salts dissociate, releasing bioavailable copper, manganese, iodine, selenium, and zinc ions. These trace elements act as cofactors for numerous enzymatic reactions, including antioxidant defense (copper‑zinc superoxide dismutase), thyroid hormone synthesis (iodine), and DNA synthesis (zinc and manganese), thereby supporting cellular metabolism and immune function.

Side Effects

Junyelt may be associated with adverse reactions typical of intravenous mineral preparations.

Common Side Effects

  • Injection site pain: mild discomfort at the infusion site.
  • Nausea: transient feeling of nausea.
  • Headache: mild headache during or after infusion.
  • Metallic taste: temporary metallic sensation in the mouth.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Hypercupremia: elevated copper levels that can cause liver dysfunction.
  • Electrolyte imbalance: abnormal serum iodine or selenium concentrations leading to thyroid or metabolic disturbances.

Precautions & Warnings

When using Junyelt, consider the following precautions to ensure safe administration.

  • Renal impairment: assess kidney function before infusion.
  • Liver disease: monitor hepatic enzymes due to copper metabolism.
  • Thyroid disorders: evaluate iodine status in patients with hyper‑ or hypothyroidism.
  • Pregnancy and lactation: use only if benefits outweigh potential risks.
  • Drug interactions: review concomitant mineral supplements to avoid excess.
  • Store at ambient temperature: keep below 25°C, protect from moisture and light, store in original container.

Avoid Interactions

Junyelt can interact with certain medications and supplements; awareness of these interactions helps prevent adverse outcomes.

Major Interactions (Avoid)

  • Chelating agents: agents such as EDTA can bind trace elements and reduce efficacy.
  • High‑dose vitamin C: may increase copper excretion and diminish therapeutic effect.

Moderate Interactions (Monitor Closely)

  • Thyroid hormones: excess iodine may alter levothyroxine dosing.
  • Anticoagulants: selenium may potentiate warfarin effect, requiring INR monitoring.
  • Other mineral supplements: concurrent zinc or copper preparations can cause overload.

Frequently Asked Questions

Junyelt is an intravenous mineral supplement that provides copper, manganese, iodine, selenium, and zinc. It is used to correct trace element deficiencies, support patients receiving total parenteral nutrition, and aid recovery after major surgery or illness where oral intake is limited.

The gluconate salts dissociate after infusion, releasing bioavailable trace elements. These act as essential cofactors for enzymes involved in antioxidant defense, thyroid hormone production, DNA synthesis, and immune function, helping restore normal metabolic activity in patients with deficiencies.

The dose of Junyelt is determined by the prescribing clinician based on the patient’s laboratory values, clinical condition, and nutritional requirements. Healthcare professionals calculate the appropriate volume and infusion rate to safely meet trace element needs.

Safety in pregnancy and lactation has not been fully established. Junyelt should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare provider.

To order Junyelt, 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.

Junyelt combines five essential trace elements in a single intravenous formulation, reducing the need for multiple separate injections. Compared with single‑element preparations, it offers convenience and consistent dosing, while still requiring monitoring to avoid excess of any individual mineral.

Junyelt should be stored at ambient temperature, preferably below 25 °C. Keep the vial in its original packaging, protect it from moisture and direct light, and avoid freezing. Inspect the solution for particulate matter before administration.

Junyelt is administered intravenously, typically as an infusion added to a compatible carrier solution. The infusion rate and duration are set by the prescribing clinician, and administration should be performed by qualified healthcare personnel in a controlled setting.

Serious risks include anaphylactic reactions, hypercupremia leading to liver injury, and electrolyte imbalances that can affect thyroid function or cause metabolic disturbances. Prompt recognition and management of these events are essential.

Patients with known hypersensitivity to any of the component gluconates, severe liver disease, uncontrolled thyroid disorders, or those who have received incompatible chelating agents should avoid Junyelt unless a clinician determines that benefits outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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