Product image of Infutraze (Zinc Chloride, Potassium Iodide, Sodium Selenite, Copper Chloride Dihydrate, Manganese Chloride Tetr) supplied by GNH India

Infutraze

Active Ingredient:
Zinc Chloride, Potassium Iodide, Sodium Selenite, Copper Chloride Dihydrate, Manganese Chloride Tetr
Origin:
EU

Infutraze (Zinc Chloride, Potassium Iodide, Sodium Selenite, Copper Chloride Dihydrate, Manganese Chloride Tetr)

Zinc chloride, potassium iodide, sodium selenite, copper chloride dihydrate, manganese chloride tetr, the active ingredients in Infutraze, is a trace element supplement presented as an intravenous solution for intravenous use. It is indicated for correction of trace element deficiency and supports patients receiving parenteral nutrition.
GNH India supplies Infutraze as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Fresenius Kabi Limited

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Indications & Clinical Uses

Infutraze is used to address deficiencies of essential trace elements in patients requiring parenteral support.

  • Trace element deficiency: restores zinc, iodine, selenium, copper and manganese to physiologic levels.
  • Parenteral nutrition support: provides the necessary trace elements for patients on total parenteral nutrition.
  • Critical illness or postoperative care: helps maintain enzymatic activity during periods of high metabolic stress.

How It Works

  • Infutraze delivers a balanced mixture of zinc, iodine, selenium, copper and manganese directly into the bloodstream, supplying cofactors required for numerous metallo‑enzymes, antioxidant defenses, thyroid hormone synthesis and cellular metabolism, thereby supporting normal biochemical pathways when oral intake is insufficient.

Side Effects

Infutraze may be associated with a range of adverse reactions.

Common Side Effects

  • Injection site pain or erythema.
  • Transient metallic taste.
  • Mild nausea or vomiting.
  • Headache.
  • Low‑grade fever.

Serious or Rare Side Effects

  • Anaphylactic or severe hypersensitivity reaction.
  • Significant electrolyte imbalance (e.g., copper or zinc overload).
  • Acute renal dysfunction.
  • Hepatotoxicity or liver enzyme elevation.

Precautions & Warnings

Use of Infutraze requires careful clinical assessment and monitoring.

  • Renal impairment: monitor serum trace element concentrations and renal function.
  • Hepatic dysfunction: observe liver enzymes during therapy.
  • Pregnancy: administer only if potential benefit justifies the risk.
  • Concurrent parenteral nutrition: avoid duplicate supplementation of trace elements.
  • Known hypersensitivity: discontinue immediately if allergic reaction occurs.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Infutraze can interact with other medications and supplements that affect trace element balance.

Major Interactions (Avoid)

  • High‑dose oral zinc supplements: may precipitate copper deficiency.
  • Thyroid hormone therapy: excess iodine can alter thyroid hormone levels.

Moderate Interactions (Monitor Closely)

  • Loop or thiazide diuretics: may modify electrolyte status.
  • Anticoagulants: trace elements can influence coagulation pathways.
  • Certain chemotherapy agents: potential additive toxicity requiring closer monitoring.

Frequently Asked Questions

Infutraze is an intravenous trace element supplement used to correct deficiencies of zinc, iodine, selenium, copper and manganese, particularly in patients receiving total parenteral nutrition or who have increased metabolic demands.

The formulation supplies essential cofactors for metallo‑enzymes, supports antioxidant defenses, participates in thyroid hormone synthesis, and contributes to cellular metabolism, thereby restoring normal biochemical functions when administered intravenously.

The dose of Infutraze is individualized; the prescribing clinician determines the amount and infusion rate based on the patient’s trace element status, clinical condition, and concurrent nutrition regimen.

Safety data are limited. Infutraze should be used in pregnancy or while breastfeeding only if the potential therapeutic benefit outweighs any possible risk to the fetus or infant, and under close medical supervision.

To order Infutraze, 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 institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed) and necessary import documentation.

Infutraze provides a balanced blend of five essential trace elements in a single IV formulation, which can simplify supplementation compared with using separate single‑element products. It is manufactured to EU standards, offering consistent quality and concentration.

Infutraze must be stored at 2‑8 °C, protected from light, and kept in its original container. It should not be frozen or shaken vigorously to maintain solution stability.

Infutraze is administered intravenously, typically added to a compatible IV fluid bag or infused directly according to the prescribing clinician’s instructions and the patient’s individual trace element needs.

Serious risks include anaphylactic reactions, severe electrolyte disturbances such as copper or zinc overload, acute renal dysfunction, and hepatotoxicity. Prompt recognition and discontinuation are essential if these events occur.

Infutraze should be avoided in patients with known hypersensitivity to any of its components, in those with uncontrolled severe renal or hepatic impairment, and in individuals where trace element supplementation is contraindicated without medical oversight.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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