Nutraferon I-TEN+ Injection

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Parenteral
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Product Discription

Nutraferon I-TEN+ Injection – for Rapid High-Dose Correction of Iron Deficiency Anaemia & Anaemia of Chronic Kidney Disease

₹480.00

Nutraferon I-TEN+ Injection – Overview

Nutraferon I-TEN+ Injection is a third-generation, dextran-free parenteral iron replacement therapy formulated with Ferric Carboxymaltose (delivering 50 mg of elemental iron per mL; typically 500 mg / 10 mL or 1000 mg / 20 mL single-use vial). It is clinically indicated to treat Iron Deficiency Anaemia (IDA)—a condition in which insufficient body iron stores lead to reduced red blood cell production and impaired systemic oxygen transport—as well as Anaemia due to Chronic Kidney Disease (CKD). Engineered for gynaecology and obstetrics, nephrology, gastroenterology, oncology, and internal medicine, Nutraferon I-TEN+ Injection is prescribed when oral iron preparations are ineffective, poorly tolerated, or blocked by intestinal malabsorption and elevated hepcidin, or when there is a clinical need to deliver iron rapidly. Unlike older parenteral iron sucrose formulations (20 mg/mL) that require multiple low-dose visits, the stable macromolecular ferric hydroxide–carboxymaltose shell of Nutraferon I-TEN+ prevents premature release of free labile iron in the bloodstream—enabling a high single dose (up to 1000 mg of elemental iron) to be administered in a single 15-minute intravenous infusion. Explore our other Nutraferon healthcare products to learn more about our product range. You can also visit our healthcare website for additional information.

Clinical Highlights

  • Macromolecular Ferric Hydroxide–Carboxymaltose Stability: Consists of a polynuclear iron(III)-hydroxide core surrounded by a non-reducing branched carboxymaltose carbohydrate shell (molecular weight ~150 kDa). This robust structure restricts ionic iron dissociation in plasma, preventing transferrin oversaturation and oxidative free-radical toxicity even at 1000 mg single doses.
  • Reticuloendothelial Macrophage Uptake & Physiological Incorporation: Following intravenous administration, the ferric carboxymaltose complex is cleared from plasma by reticuloendothelial macrophages in the bone marrow, liver, and spleen (terminal half-life ~7 to 12 hours). Within macrophage endolysosomes, iron is released from the carbohydrate shell, stored safely in intracellular ferritin, or exported via ferroportin to circulating transferrin for transport to erythroid precursors and synthesis of functional hemoglobin and myoglobin.
  • Rapid Erythropoietic & Ferritin Response: Reticulocyte counts increase within 3 to 5 days, serum ferritin and transferrin saturation (TSAT) normalize rapidly, and hemoglobin concentrations typically rise by 2 to 3 g/dL within 2 to 4 weeks.

Key Benefits

  • Rapid Single-Dose Iron Replenishment (Up to 1000 mg in 15 Minutes): High 50 mg/mL concentration and tight carbohydrate complex stability allow full or near-full iron deficit correction in just 1 to 2 clinical visits.
  • Effectively Treats Anaemia of Chronic Kidney Disease (CKD): Overcomes functional and absolute iron deficiency in both non-dialysis and haemodialysis CKD patients, optimizing response to erythropoiesis-stimulating agents (ESAs) and reducing blood transfusion needs.
  • Bypasses Intestinal Malabsorption & Hepcidin Blockade: Ideal for patients with Inflammatory Bowel Disease (IBD), celiac disease, bariatric surgery, chronic gastrointestinal bleeding, or chemotherapy-induced anaemia where gut iron uptake fails.
  • Accelerates Obstetric, Postpartum & Gynaecological Recovery: Rapidly restores hemoglobin and serum ferritin in heavy menstrual bleeding (menorrhagia), postpartum haemorrhage anaemia, and second-/third-trimester gestational iron deficiency anaemia.
  • Dextran-Free Complex with Low Immunogenicity: Contains no dextran and does not cross-react with anti-dextran antibodies, eliminating the requirement for a pre-infusion test dose while maintaining a physiological pH (5.0–7.0) and osmolarity.

Directions of Use & Safety Information

  • Strictly Professional Clinical Administration Only: Your physician, clinician, or registered nurse will administer this medicine in a clinic or hospital equipped to monitor and manage hypersensitivity reactions. Kindly do not self-administer. Administer exclusively by the Intravenous (IV) route (via slow undiluted IV bolus injection or diluted IV drip infusion). Never administer Intramuscularly (IM) or Subcutaneously (SC).
  • Standard Dosing & Dilution Protocol (50 mg Elemental Iron / mL):
    • Maximum Single & Weekly Dose: Up to 1000 mg of elemental iron (20 mL) in a single session (not exceeding 15 mg to 20 mg iron/kg body weight), and no more than 1000 mg of iron per week.
    • Diluent & Minimum Concentration Rule (Pharmacist Alert): For IV drip infusion, dilute ONLY in sterile 0.9% Sodium Chloride (Normal Saline). Never dilute below 2 mg of elemental iron per mL (for example, 500 mg [10 mL] in a maximum of 100 mL 0.9% NaCl infused over at least 6 minutes; 500–1000 mg [10–20 mL] in a maximum of 250 mL 0.9% NaCl infused over at least 15 minutes), as over-dilution or dilution in Dextrose destabilizes the colloidal iron-carbohydrate complex!
  • Extravasation & Post-Infusion Monitoring: Ensure secure IV cannula placement prior to infusion; paravenous leakage (extravasation) of Ferric Carboxymaltose can cause pain, inflammation, and long-lasting brown discoloration (hemosiderin staining) of the skin at the injection site. Observe every patient for at least 30 minutes after each injection for signs of hypersensitivity or transient blood pressure elevation.

FAQs

Disclaimer

Prescription Only Medicine (POM — Hospital / Clinical IV Use Only). Strictly contraindicated in patients with known hypersensitivity to ferric carboxymaltose or other parenteral iron preparations, anaemia not attributed to iron deficiency (e.g., thalassemia or hemolytic anaemia), evidence of iron overload (hemochromatosis or hemosiderosis), and during the first trimester of pregnancy. Store below 30°C in original carton protected from light; do not freeze. Keep out of reach of children.

Reviews

Description

Nutraferon I-TEN+ Injection – Overview

Nutraferon I-TEN+ Injection is a third-generation, dextran-free parenteral iron replacement therapy formulated with Ferric Carboxymaltose (delivering 50 mg of elemental iron per mL; typically 500 mg / 10 mL or 1000 mg / 20 mL single-use vial). It is clinically indicated to treat Iron Deficiency Anaemia (IDA)—a condition in which insufficient body iron stores lead to reduced red blood cell production and impaired systemic oxygen transport—as well as Anaemia due to Chronic Kidney Disease (CKD).

Engineered for gynaecology and obstetrics, nephrology, gastroenterology, oncology, and internal medicine, Nutraferon I-TEN+ Injection is prescribed when oral iron preparations are ineffective, poorly tolerated, or blocked by intestinal malabsorption and elevated hepcidin, or when there is a clinical need to deliver iron rapidly. Unlike older parenteral iron sucrose formulations (20 mg/mL) that require multiple low-dose visits, the stable macromolecular ferric hydroxide–carboxymaltose shell of Nutraferon I-TEN+ prevents premature release of free labile iron in the bloodstream—enabling a high single dose (up to 1000 mg of elemental iron) to be administered in a single 15-minute intravenous infusion.

Explore our other Nutraferon healthcare products to learn more about our product range. You can also visit our healthcare website for additional information.

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Atchuta Rao Kavuri
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good product
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Satish R
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Excellent quality full range of products at reasonable price.
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Srujan Raga
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Good products and Good customer care and perfect and in time delivery for every clients . Pan India delivery 🚚 and Amazon and Tata 1 Mg products are available 💊 💉 #Nutraferon Pvt LTD#Hyderabad #Telangana #India
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MAHERUNNISA BEGUM
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Roronoa Zoro
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Nice product with good ingredients.
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Vijay Chowdary
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Good working
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joynikhil
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