Product image of Nephroferol (Iron Sucrose) supplied by GNH India

Nephroferol

Active Ingredient:
Iron Sucrose
Origin:
EU

Nephroferol (Iron Sucrose)

Iron sucrose, the active ingredient in Nephroferol, is an iron preparation presented as an intravenous solution for intravenous use. It treats iron deficiency anemia and anemia of chronic kidney disease by replenishing depleted iron stores.
GNH India supplies Nephroferol as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Verisfield S.M.S.A

1
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Indications & Clinical Uses

Nephroferol is used to correct iron deficiency in conditions where oral iron is ineffective or not tolerated.

  • Iron deficiency anemia: restores hemoglobin levels and improves symptoms of fatigue.
  • Anemia of chronic kidney disease: replenishes iron stores to support erythropoiesis in dialysis and non‑dialysis patients.
  • Patients receiving erythropoiesis‑stimulating agents: enhances response to therapy by providing necessary iron for red blood cell production.

How It Works

  • Iron sucrose delivers bioavailable iron directly into the bloodstream, where it binds to transferrin and is transported to the bone marrow. Inside the marrow, iron is incorporated into developing hemoglobin molecules, allowing red blood cells to mature and increasing the total iron reserve in the body.

Side Effects

Common Side Effects

  • Nausea: mild to moderate upset stomach after infusion.
  • Headache: transient headache during or after administration.
  • Muscle cramps: occasional cramping of limbs.
  • Hypotension: temporary drop in blood pressure during infusion.
  • Injection site pain: local discomfort at the IV site.
  • Metallic taste: brief metallic sensation in the mouth.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Severe hypotension: marked blood pressure decline needing intervention.
  • Iron overload: excessive iron accumulation with long‑term use.
  • Cardiac arrest: rare but life‑threatening event.
  • Acute respiratory distress: sudden breathing difficulty.
  • Serum sickness-like reaction: fever, rash, and joint pain.

Precautions & Warnings

Nephroferol should be administered under medical supervision with appropriate monitoring.

  • Monitor iron parameters: check ferritin and transferrin saturation before and during therapy.
  • Assess for hypersensitivity: discontinue if signs of allergic reaction appear.
  • Use caution in cardiac disease: watch for hypotension and arrhythmias.
  • Avoid in active infection: iron can promote bacterial growth.
  • Administer by trained personnel: ensure proper IV technique and infusion rate.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Nephroferol may interact with other agents that affect iron metabolism or cardiovascular status.

Major Interactions (Avoid)

  • Concurrent IV iron products: risk of iron overload.
  • High‑dose parenteral vitamin C: increases free iron and oxidative stress.
  • Certain antihypertensives: may exacerbate hypotension during infusion.

Moderate Interactions (Monitor Closely)

  • Erythropoiesis‑stimulating agents: may require dose adjustment of iron.
  • Oral phosphate binders: can reduce iron absorption if given simultaneously.

Frequently Asked Questions

Nephroferol is an intravenous iron sucrose formulation used to treat iron deficiency anemia and anemia associated with chronic kidney disease, especially when oral iron therapy is insufficient or not tolerated.

Iron sucrose provides readily available iron that binds to transferrin in the bloodstream, delivering the element to the bone marrow where it is incorporated into hemoglobin, supporting red blood cell production and restoring iron stores.

The prescribed dose of Nephroferol is determined by the treating physician based on the patient’s iron deficiency severity, weight, and clinical response. Dosing regimens are individualized and should follow the prescriber’s instructions.

Safety data for iron sucrose in pregnancy and lactation are limited. The product should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and under close medical supervision.

To order Nephroferol, submit an enquiry on the product page at gnhindia.com with 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.

Nephroferol (iron sucrose) is a low‑molecular‑weight IV iron that offers rapid infusion and a favorable safety profile compared with larger iron complexes. It provides controlled iron release, reducing the risk of severe hypersensitivity reactions seen with some alternative IV iron formulations.

Nephroferol must be stored at 2‑8 °C, protected from light, and should not be frozen or shaken. Keep the vial in its original packaging until use to maintain stability and sterility.

Nephroferol is given as an intravenous infusion by a qualified healthcare professional. The infusion rate and total dose are set by the prescriber, and patients are monitored for any adverse reactions during and after the administration.

The most serious risks include severe hypersensitivity reactions such as anaphylaxis, significant hypotension, and iron overload with prolonged use. Immediate medical attention is required if any signs of a severe reaction occur.

Nephroferol is contraindicated in patients with known hypersensitivity to iron sucrose or any component of the formulation, and it should be used with caution in individuals with active infections, severe cardiac disease, or uncontrolled hypertension.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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