Iron Sucrose
Parenteral repletion becomes necessary when oral iron is not tolerated or not absorbed, and iron sucrose is one of the intravenous preparations used in that situation. Chronic kidney disease is the setting in which it is most often required, since both absorption and utilisation of oral iron are impaired in that population. The sucrose carrier stabilises the iron core and releases it in a controlled manner, a design associated with a lower risk of hypersensitivity reaction than some earlier injectable iron products. Treatment aims to rebuild haemoglobin concentration and replenish tissue iron stores in iron deficiency anaemia. The preparation is an approved agent that has reached the final phase of clinical development.
This intravenous iron preparation provides iron directly into the bloodstream for patients with iron deficiency anemia who cannot take or absorb oral iron, particularly those with chronic kidney disease. The sucrose carrier stabilizes the iron and helps reduce the risk of allergic reactions compared to some other injectable iron preparations. It is used to restore hemoglobin levels and iron stores.
치료 영역
Pharmacokinetics (PK)
Pharmacodynamics (PD)
HBD / HBA
- / -
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
자주 묻는 질문
This intravenous iron preparation provides iron directly into the bloodstream for patients with iron deficiency anemia who cannot take or absorb oral iron, particularly those with chronic kidney disease. The sucrose carrier stabilizes the iron and helps reduce the risk of allergic reactions compared to some other injectable iron preparations. It is used to restore hemoglobin levels and iron stores.
Yes, Iron Sucrose is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1200823. Open-access bioactivity database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-08-20.
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