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

Intrafer

Active Ingredient:
Iron Sucrose
Origin:
EU

Intrafer (Iron Sucrose)

Iron sucrose, the active ingredient in Intrafer, is an iron preparation presented as an intravenous solution for intravenous use. It treats iron deficiency anemia and is used in patients with chronic kidney disease to replenish iron stores and support hemoglobin synthesis.

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

Manufacturer / TM Owner

Vianex S.A.

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Indications & Clinical Uses

Intrafer (iron sucrose) is employed to manage conditions related to iron deficiency and anemia.

  • Iron deficiency anemia: restores hemoglobin levels and replenishes depleted iron stores.
  • Anemia associated with chronic kidney disease: provides elemental iron for hemoglobin synthesis in patients receiving dialysis or other CKD therapies.

How It Works

  • Iron sucrose is a parenteral iron complex that releases iron in a controlled manner after intravenous administration. The released iron binds to plasma transferrin, which transports it to the bone marrow where it is incorporated into developing red blood cells, facilitating hemoglobin synthesis and correcting iron deficiency.

Side Effects

Common Side Effects

  • Nausea: mild to moderate discomfort in the stomach.
  • Headache: transient pain often occurring during or after infusion.
  • Muscle cramps: involuntary tightening of muscles, usually in the limbs.
  • Injection site pain: local discomfort at the site of administration.
  • Flushing: temporary reddening and warmth of the skin.
  • Hypertension: temporary rise in blood pressure during infusion.

Serious or Rare Side Effects

  • Anaphylactic reaction: severe, potentially life‑threatening allergic response.
  • Hypotension: sudden drop in blood pressure requiring monitoring.
  • Acute respiratory distress: difficulty breathing that may develop rapidly.
  • Iron overload: excessive iron accumulation leading to organ damage.
  • Arrhythmia: irregular heart rhythm that may require medical attention.

Precautions & Warnings

Before using Intrafer, consider the following precautions:

  • Renal impairment: monitor iron parameters and renal function closely.
  • Cardiovascular disease: observe blood pressure during and after infusion.
  • History of hypersensitivity: avoid if the patient has previously reacted to iron sucrose.
  • Pregnancy and lactation: use only if clearly needed after risk‑benefit assessment.
  • Concurrent erythropoiesis‑stimulating agents: adjust dosing to prevent excessive hemoglobin rise.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Intrafer may interact with other medications as follows.

Major Interactions (Avoid)

  • Concurrent parenteral iron products: increase risk of iron overload.
  • High‑dose vitamin C infusion: may enhance free iron release and toxicity.
  • Iron chelating agents (e.g., deferoxamine): bind administered iron and reduce efficacy.

Moderate Interactions (Monitor Closely)

  • Erythropoiesis‑stimulating agents: may potentiate hemoglobin increase, requiring dose adjustment.
  • Antihypertensive drugs: monitor blood pressure due to possible infusion‑related hypertension.
  • Oral phosphate binders: may interfere with laboratory assessment of iron parameters.

Frequently Asked Questions

Intrafer is a parenteral iron formulation indicated for the treatment of iron deficiency anemia and for correcting anemia in patients with chronic kidney disease. It provides elemental iron needed for hemoglobin synthesis and helps restore normal iron stores in these conditions.

Iron sucrose delivers iron directly into the bloodstream, where it binds to transferrin, the main iron‑transport protein. The iron‑transferrin complex is then taken up by the bone marrow, where it is incorporated into developing red blood cells, supporting hemoglobin production and correcting iron deficiency.

The dose of Intrafer is individualized by the prescribing healthcare professional based on the patient’s iron deficiency severity, body weight, and clinical response. The prescriber determines the total iron requirement and the infusion schedule according to established guidelines.

Intrafer should be used in pregnancy or while breastfeeding only if clearly needed and after a careful risk‑benefit assessment by the treating physician. Limited data are available, so the decision must be individualized for each patient.

To order Intrafer, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain handling if required) and import documentation.

Intrafer (iron sucrose) is a low‑molecular‑weight iron complex that releases iron more gradually than some high‑dose iron dextran products, resulting in a lower incidence of severe allergic reactions. It is commonly preferred for patients needing controlled iron delivery and for use in dialysis settings.

Intrafer must be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze or shake the solution. Keep the product in its original packaging until ready for use to maintain stability and sterility.

Intrafer is administered as an intravenous infusion by a qualified healthcare professional. The infusion rate and duration are determined by the prescriber, typically over a period of 15‑30 minutes, with monitoring for any adverse reactions during and after the infusion.

The most serious risks include severe hypersensitivity reactions such as anaphylaxis, acute hypotension or hypertension, and iron overload if administered in excess. Patients should be monitored closely during infusion, and any signs of severe reaction require immediate medical intervention.

Intrafer should not be used in patients with known hypersensitivity to iron sucrose or any component of the formulation, in those with active infections that could be exacerbated by iron, or in patients with severe iron overload conditions unless specifically directed by a specialist.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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