Product image of Olitrace (Sodium Molybdate Dihydrate, Zinc Chloride, Chromic Chloride, Copper Chloride, Ferrous Chloride, Mang) supplied by GNH India

Olitrace

Active Ingredient:
Sodium Molybdate Dihydrate, Zinc Chloride, Chromic Chloride, Copper Chloride, Ferrous Chloride, Mang
Origin:
EU

Olitrace (Sodium Molybdate Dihydrate, Zinc Chloride, Chromic Chloride, Copper Chloride, Ferrous Chloride, Mang)

Sodium Molybdate Dihydrate, the active ingredient in Olitrace, is a trace element supplement presented as a sterile aqueous solution for parenteral use. It provides essential minerals that support enzymatic functions in patients requiring parenteral nutrition. GNH India supplies Olitrace as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and transplant centres worldwide.

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

Manufacturer / TM Owner

B.Braun Melsungen Ag

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Indications & Clinical Uses

Olitrace is used as a multi‑trace element supplement in clinical nutrition, supporting patients who receive parenteral nutrition.

  • Premature infants: helps meet essential trace element requirements for growth and development.
  • Adult patients on long‑term parenteral nutrition: maintains adequate levels of molybdenum, zinc, chromium, copper, iron and manganese.
  • Post‑surgical or trauma patients: supports metabolic processes that rely on trace elements.
  • Patients with malabsorption syndromes: provides trace elements that are poorly absorbed orally.
  • Renal replacement therapy patients: assists in maintaining trace element balance during dialysis.

How It Works

  • Olitrace delivers a combination of essential trace elements directly into the bloodstream, bypassing intestinal absorption. These minerals act as cofactors for various enzymes involved in oxidative metabolism, nucleic acid synthesis, and immune function, ensuring that critical biochemical pathways operate efficiently in patients dependent on parenteral nutrition.

Side Effects

Olitrace may be associated with infusion‑related reactions and laboratory‑detected abnormalities.

Common Side Effects

  • Mild erythema at the infusion site: transient redness that resolves without intervention.
  • Low‑grade fever: temporary temperature elevation that subsides spontaneously.
  • Transient increase in serum copper or zinc levels: laboratory finding without clinical symptoms.

Serious or Rare Side Effects

  • Anaphylactic reaction: acute hypersensitivity requiring immediate medical management.
  • Severe hypermagnesium (if formulation contains magnesium): may cause cardiac rhythm disturbances.
  • Acute hemolysis: rapid destruction of red blood cells observed in rare cases.
  • Metabolic acidosis: significant pH imbalance requiring corrective therapy.

Precautions & Warnings

When using Olitrace, clinicians should assess trace element status and monitor laboratory values regularly.

  • Assess baseline trace element levels: obtain serum concentrations before initiating therapy.
  • Monitor serum concentrations: repeat testing weekly or as clinically indicated.
  • Adjust dosage in renal impairment: reduce or space infusions based on renal function.
  • Avoid concurrent high‑dose oral trace supplements: risk of excess accumulation.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Olitrace can interact with other medications that influence mineral balance or cause infusion reactions.

Major Interactions (Avoid)

  • High‑dose intravenous iron preparations: may cause excessive iron load and oxidative stress.

Moderate Interactions (Monitor Closely)

  • Chelating agents (e.g., deferoxamine): may reduce the effectiveness of administered trace elements.
  • Antacids containing aluminum or magnesium: can alter absorption if oral supplements are added.
  • Certain antibiotics (e.g., tetracyclines): may bind trace metals and affect their activity.
  • Loop diuretics: increase urinary excretion of zinc and copper, requiring closer monitoring.
  • Vitamin C high‑dose infusion: enhances copper absorption, potentially leading to excess levels.

Frequently Asked Questions

Olitrace is a sterile aqueous solution that provides a blend of essential trace elements for patients receiving parenteral nutrition. It is used to prevent or correct deficiencies of molybdenum, zinc, chromium, copper, iron and manganese in clinical settings such as intensive care, neonatal care, and long‑term home nutrition.

Sodium molybdate supplies molybdenum, a cofactor for enzymes like sulfite oxidase and xanthine oxidase. These enzymes participate in sulfur amino‑acid metabolism and purine catabolism, supporting normal cellular function and detoxification pathways when delivered intravenously.

The dose of Olitrace is individualized by the prescribing clinician based on the patient’s age, weight, renal function and laboratory‑measured trace element levels. Healthcare professionals calculate the appropriate infusion volume and frequency to meet the patient’s specific nutritional needs.

Olitrace may be used during pregnancy or lactation only when clearly indicated and prescribed by a qualified healthcare provider. The benefits of correcting trace element deficiencies must be weighed against potential risks, and the decision should be made on a case‑by‑case basis.

To order Olitrace, 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.

Olitrace combines six trace elements in a single sterile solution, reducing the need for multiple separate infusions. Compared with products that contain only one or two minerals, Olitrace offers a broader spectrum of essential cofactors, which can simplify administration and improve compliance in complex parenteral nutrition regimens.

Olitrace should be stored at 2‑8°C, protected from light, and kept in its original container. Do not freeze or vigorously shake the solution. Before use, inspect the vial for particulates or discoloration and allow it to reach room temperature if required for infusion.

Olitrace is administered intravenously, typically added to a compatible parenteral nutrition bag or infused separately according to the prescribing clinician’s instructions. The infusion rate and volume are adjusted to the patient’s needs and monitored for any adverse reactions during administration.

Serious risks include anaphylactic reactions, severe hyper‑metallic states (e.g., copper or zinc toxicity), acute hemolysis and metabolic acidosis. Prompt recognition and management of these events are essential, and regular laboratory monitoring helps mitigate the likelihood of severe complications.

Olitrace is contraindicated in patients with known hypersensitivity to any of its components, those with severe copper or zinc overload, and individuals receiving incompatible intravenous medications that may precipitate metal salts. Clinicians should also exercise caution in patients with significant renal or hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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