Product image of Ijzer (Iii)carboxymaltose Viatris (Iron) supplied by GNH India

Ijzer (Iii)carboxymaltose Viatris

Active Ingredient:
Iron
Origin:
EU

Ijzer (Iii)carboxymaltose Viatris (Iron)

Ferric carboxymaltose, the active ingredient in Ijzer (III)carboxymaltose Viatris, is an iron supplement presented as an injection solution for intravenous use. It treats iron deficiency anemia in patients who require rapid replenishment of iron stores, including adults and children with chronic conditions.
GNH India supplies Ijzer (III)carboxymaltose Viatris as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Viatris Limited

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Indications & Clinical Uses

Ijzer (III)carboxymaltose Viatris is used to correct iron deficiency anemia across several clinical settings.

  • Iron deficiency anemia: restores hemoglobin levels and replenishes depleted iron stores.
  • Iron deficiency anemia in chronic kidney disease: supports erythropoiesis when oral iron is ineffective.
  • Iron deficiency anemia in perioperative patients: provides rapid iron repletion before surgery to reduce transfusion needs.

How It Works

  • Ferric carboxymaltose delivers a stable iron-carbohydrate complex that releases elemental iron in a controlled manner after intravenous administration. The iron is taken up by reticuloendothelial cells, transferred to transferrin, and incorporated into hemoglobin within developing red blood cells, thereby correcting iron deficiency and supporting normal erythropoiesis.

Side Effects

Adverse reactions may occur following intravenous administration of ferric carboxymaltose.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Headache: transient cranial discomfort.
  • Injection site pain: local tenderness or erythema.
  • Transient hypotension: brief drop in blood pressure during infusion.
  • Metallic taste: temporary alteration of taste perception.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Severe hypotension: marked blood pressure decline possibly leading to syncope.
  • Hypophosphatemia: significant drop in serum phosphate levels.
  • Acute respiratory distress: sudden breathing difficulty.
  • Severe skin reactions: such as Stevens‑Johnson syndrome.

Precautions & Warnings

Use of ferric carboxymaltose requires careful clinical assessment and monitoring.

  • Baseline assessment: confirm iron deficiency with laboratory tests before administration.
  • Hemoglobin monitoring: check levels periodically to avoid excessive iron loading.
  • Hypersensitivity caution: avoid in patients with known allergy to ferric carboxymaltose or other IV iron products.
  • Infusion rate: administer at recommended rate to reduce risk of hypotension.
  • Phosphate monitoring: observe serum phosphate during and after treatment.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Ferric carboxymaltose may interact with other medications, affecting safety or efficacy.

Major Interactions (Avoid)

  • Concurrent IV iron products: risk of iron overload.
  • Known hypersensitivity to ferric carboxymaltose: may trigger severe allergic reactions.
  • Parenteral iron dextran: combined use can increase toxicity.

Moderate Interactions (Monitor Closely)

  • Oral iron supplements: may reduce absorption of each other; stagger dosing.
  • Erythropoiesis‑stimulating agents: enhanced hematologic response, monitor hemoglobin.
  • Tetracycline antibiotics: possible chelation reducing antibiotic effectiveness.
  • Phosphate binders: may exacerbate hypophosphatemia.
  • Antihypertensive drugs: monitor blood pressure due to potential hypotensive effect.

Frequently Asked Questions

Ijzer (III)carboxymaltose Viatris is an intravenous iron formulation indicated for the treatment of iron deficiency anemia. It is used when rapid replenishment of iron stores is needed, such as in patients with chronic kidney disease, postoperative anemia, or when oral iron therapy is ineffective or not tolerated.

Ferric carboxymaltose provides a stable iron‑carbohydrate complex that releases elemental iron after intravenous infusion. The iron is taken up by macrophages, bound to transferrin, and delivered to the bone marrow where it is incorporated into hemoglobin, thereby correcting the deficit and supporting red blood cell production.

The prescribed dose of Ijzer (III)carboxymaltose Viatris is determined by the treating physician based on the patient’s hemoglobin level, body weight, and iron deficit. The healthcare professional calculates the total iron requirement and selects the appropriate infusion volume and rate.

Safety data for ferric carboxymaltose in pregnancy and lactation are limited, and the product is classified as pregnancy category unknown. Use only if the potential benefit justifies the potential risk, and the decision should be made by a qualified healthcare provider.

To place an order, 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 necessary import documentation.

Compared with older IV iron formulations, ferric carboxymaltose allows larger single‑dose administrations with a lower risk of severe hypersensitivity reactions. It also has a relatively rapid infusion time and a favorable safety profile, making it a preferred option for many clinicians when rapid iron repletion is required.

The product must be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. Prior to use, inspect the vial for particulate matter and ensure the solution is clear. Follow aseptic technique during preparation and administration.

Ijzer (III)carboxymaltose is given as an intravenous infusion. The healthcare professional selects the appropriate infusion volume based on the calculated iron dose and administers it over the recommended time, typically not exceeding 15 minutes for doses up to 1000 mg of elemental iron.

Serious risks include anaphylactic reactions, severe hypotension, and profound hypophosphatemia, which can lead to muscle weakness or bone pain. Immediate medical attention is required if any signs of severe allergic reaction or sudden drop in blood pressure occur during or after infusion.

Patients with known hypersensitivity to ferric carboxymaltose or any component of the formulation should avoid this product. It is also contraindicated in individuals who have experienced severe reactions to other intravenous iron preparations. Clinical judgment is required for patients with active infections or uncontrolled hypertension.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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