Product image of Nefro-Fer (Iron Sucrose) supplied by GNH India

Nefro-Fer

Active Ingredient:
Iron Sucrose
Origin:
EU

Nefro-Fer (Iron Sucrose)

Iron Sucrose, the active ingredient in Nefro-Fer, is a iron preparation presented as a injection for intravenous use. It treats iron deficiency anemia, including anemia associated with chronic kidney disease, in patients requiring parenteral iron therapy. It is approved in the European Union and is administered under medical supervision.

GNH India supplies Nefro-Fer as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide, with a focus on quality assurance and regulatory compliance globally.

Manufacturer / TM Owner

Medice Arzneimittel Pütter Gmbh & Co. Kg

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Indications & Clinical Uses

Iron sucrose is used to correct iron deficiency in conditions where oral iron is insufficient or not tolerated.

  • Iron deficiency anemia: restores hemoglobin levels and replenishes iron stores.
  • Anemia associated with chronic kidney disease: provides intravenous iron to support erythropoiesis in CKD patients.
  • Peri‑operative anemia management: improves iron status before surgery to reduce transfusion need.

How It Works

  • Iron sucrose is a stable iron‑carbohydrate complex that releases elemental iron after intravenous administration. The iron is taken up by reticuloendothelial cells, bound to transferrin, and delivered to the bone marrow for incorporation into hemoglobin, thereby correcting iron deficiency and supporting erythropoiesis. The controlled release limits free iron, reducing oxidative stress, and the complex is cleared within hours, providing a predictable pharmacokinetic profile.

Side Effects

Iron sucrose may be associated with a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Nausea: mild gastrointestinal upset.
  • Headache: transient headache.
  • Injection site pain: discomfort at infusion site.
  • Muscle cramps: occasional cramping.

Serious or Rare Side Effects

  • Hypotension: sudden drop in blood pressure during infusion.
  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Iron overload: excessive iron accumulation with prolonged use.
  • Hepatotoxicity: liver enzyme elevations in rare cases.

Precautions & Warnings

When using iron sucrose, clinicians should observe several safety measures.

  • Assess iron status: confirm iron deficiency before initiating therapy.
  • Monitor hemoglobin: check levels regularly to evaluate response.
  • Observe during infusion: watch for hypotension or allergic reactions.
  • Avoid in patients with known hypersensitivity to iron sucrose or its components.
  • Use caution in patients with active infections or liver disease.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Iron sucrose can interact with other medicines, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Concurrent use of other intravenous iron products: may cause iron overload.
  • High-dose vitamin C: increases iron absorption and risk of toxicity.
  • Certain antibiotics (e.g., quinolones): may chelate iron, reducing efficacy.

Moderate Interactions (Monitor Closely)

  • Oral iron supplements: may interfere with laboratory measurement of iron parameters.
  • Antihypertensive agents: hypotensive episodes may be potentiated during infusion.
  • Erythropoiesis‑stimulating agents: may enhance erythropoietic response, requiring dose adjustment.

Frequently Asked Questions

Nefro-Fer is an intravenous iron sucrose product used to treat iron deficiency anemia and anemia associated with chronic kidney disease, especially when oral iron therapy is ineffective, not tolerated, or when rapid replenishment of iron stores is required.

Iron sucrose delivers elemental iron directly into the bloodstream. The iron is captured by reticuloendothelial cells, bound to transferrin, and transported to the bone marrow where it is incorporated into hemoglobin, thereby restoring normal red blood cell production.

The dose of Nefro-Fer is individualized by the prescribing clinician based on the patient’s iron deficit, body weight, and clinical condition. Dosing regimens are determined in a medical setting and are not standardized in public information.

Safety data for iron sucrose in pregnancy and lactation are limited. Use is generally considered only when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision should be made by a qualified health professional.

To order Nefro-Fer, 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.

Compared with oral iron salts, Nefro-Fer provides a faster increase in iron stores and avoids gastrointestinal side effects. Relative to other IV iron products such as ferric gluconate, iron sucrose has a well‑characterized safety profile and allows for controlled dosing in smaller infusion volumes.

Nefro-Fer must be stored refrigerated at 2‑8 °C, protected from light, and should never be frozen or shaken. The product should be kept in its original packaging until ready for use to maintain stability.

Nefro-Fer is given as an intravenous infusion by a qualified health professional. The infusion is typically administered over a period of 15–30 minutes, with the patient monitored for any immediate adverse reactions during and after the procedure.

The most serious risks include acute hypotension, severe allergic reactions such as anaphylaxis, and iron overload with prolonged or excessive dosing. Prompt recognition and management of these events are essential during and after infusion.

Nefro-Fer should be avoided in patients with known hypersensitivity to iron sucrose or any of its excipients, in those with active severe infections, and in individuals with uncontrolled hypertension or severe liver disease unless the benefits clearly outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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