Product image of Injectafer (Ferric Carboxymaltose) supplied by GNH India

Injectafer

Active Ingredient:
Ferric Carboxymaltose
Origin:
EU

Injectafer (Ferric Carboxymaltose)

Ferric Carboxymaltose, the active ingredient in Injectafer, is an iron preparation presented as an injectable solution for intravenous use. It treats iron deficiency anemia, primarily in adults who require rapid iron repletion, such as those with chronic kidney disease, gastrointestinal blood loss, or intolerance to oral iron.

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

Manufacturer / TM Owner

Vifor France

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Indications & Clinical Uses

Injectafer is an intravenous iron formulation used to correct iron deficiency anemia across several clinical settings.

  • Iron deficiency anemia: restores depleted iron stores and raises hemoglobin levels.
  • Chronic kidney disease‑associated anemia: provides rapid iron repletion when oral iron is ineffective.
  • Inflammatory bowel disease‑related iron deficiency: corrects anemia caused by malabsorption.
  • Pre‑operative anemia: improves hemoglobin before surgery to reduce transfusion risk.

How It Works

  • Ferric carboxymaltose delivers a stable iron complex that releases elemental iron after intravenous administration. The iron is taken up by reticuloendothelial cells, incorporated into ferritin, and subsequently transferred to transferrin for delivery to the bone marrow, where it supports hemoglobin synthesis and restores normal erythropoiesis.

Side Effects

Injectafer may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Nausea: transient feeling of stomach upset.
  • Headache: mild to moderate intensity.
  • Injection site pain: localized discomfort at the infusion site.
  • Transient hypotension: brief drop in blood pressure during or shortly after infusion.
  • Metallic taste: brief alteration in taste perception.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Severe hypotension: marked blood pressure decline that may need intervention.
  • Hypersensitivity reactions: rash, urticaria, or bronchospasm.
  • Iron overload: excessive iron accumulation with potential organ damage.
  • Acute respiratory distress: sudden breathing difficulty.
  • Myocardial infarction: rare cardiac event linked to rapid iron release.

Precautions & Warnings

Injectafer should be used with careful clinical assessment and monitoring.

  • Assess iron status: confirm iron deficiency before initiating therapy.
  • Monitor hematology: check hemoglobin and ferritin levels during treatment.
  • Hypersensitivity caution: avoid in patients with known severe reactions to IV iron.
  • Infusion rate control: administer at recommended rate to reduce hypotension risk.
  • Infection consideration: evaluate active infections before use.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Injectafer can interact with other agents that affect iron metabolism or cause additive adverse effects.

Major Interactions (Avoid)

  • Concurrent IV iron products: may cause iron overload.
  • Known hypersensitivity to dextran or other iron complexes: risk of severe allergic reaction.
  • High‑dose vitamin C administered intravenously: can increase free iron and toxicity.

Moderate Interactions (Monitor Closely)

  • Oral iron supplements taken simultaneously: may reduce absorption of each other.
  • Antacids containing aluminum or magnesium: can interfere with iron availability.
  • Tetracycline antibiotics: may chelate iron and diminish antibiotic efficacy.

Frequently Asked Questions

Injectafer is an intravenous iron formulation indicated for the treatment of iron deficiency anemia in adults, especially when rapid iron repletion is needed or oral iron therapy is ineffective, such as in chronic kidney disease, inflammatory bowel disease, or pre‑operative settings.

Ferric carboxymaltose delivers a stable iron complex that, after intravenous infusion, is taken up by reticuloendothelial cells, stored as ferritin, and then transferred to transferrin. This process supplies elemental iron for hemoglobin synthesis, restoring normal red blood cell production.

The prescribed dose of Injectafer is individualized by the treating clinician based on the patient’s iron deficit, body weight, and clinical condition. The prescriber determines the total iron requirement and the appropriate infusion schedule.

The safety of Injectafer in pregnancy and lactation has not been fully established. It should be used only if the potential benefit justifies any potential risk to the fetus or infant, and the decision should be made by a qualified healthcare professional.

To order Injectafer, 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 handling if needed), and import documentation.

Injectafer (ferric carboxymaltose) allows administration of larger single‑dose infusions compared with some older IV iron formulations, reducing the number of visits. It has a favorable safety profile but, like all IV iron, requires monitoring for hypersensitivity and hypotension. Choice of product depends on clinical needs, dosing convenience, and individual patient tolerance.

Injectafer must be stored refrigerated at 2‑8 °C, protected from light, and should never be frozen or shaken. Keep the product in its original packaging until use to maintain stability and sterility.

Injectafer is given as an intravenous infusion by a qualified healthcare professional. The infusion rate and total dose are determined by the prescriber, and the product should be administered using aseptic technique through a suitable IV line.

Serious risks include anaphylactic or severe hypersensitivity reactions, profound hypotension, iron overload, and rare events such as acute respiratory distress or myocardial infarction. Immediate medical attention is required if any signs of severe reaction occur during or after infusion.

Injectafer should not be used in patients with known hypersensitivity to ferric carboxymaltose or any component of the formulation, or in those who have experienced severe reactions to other intravenous iron products. Caution is also advised for patients with active infections or uncontrolled hypertension.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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