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IV Iron — Anaemia

Iron Sucrose

Brand names: Venofer

Iron sucrose is an intravenous iron preparation used to treat iron-deficiency anaemia when oral iron is ineffective, not tolerated, or rapid replenishment is needed, for example in chronic kidney disease.

Dosing — being independently re-sourced

ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.

Clinical monograph

How it works

The iron-sucrose complex is taken up by the reticuloendothelial system, releasing iron that is incorporated into ferritin stores and transferrin for delivery to the bone marrow to support erythropoiesis.

Prescribing in practice

  • Hypersensitivity and anaphylactoid reactions can occur with intravenous iron, so administer only where resuscitation facilities are available and observe the patient during and after the infusion.
  • Avoid in the first trimester of pregnancy and use intravenous iron only when clearly required thereafter.
  • Extravasation can cause persistent brown skin staining, so secure venous access and stop immediately if leakage is suspected.

Monitoring

Monitor for hypersensitivity during and after administration and reassess haemoglobin and iron indices (such as ferritin and transferrin saturation) to guide further dosing.

Counselling the patient

  • Report any itching, rash, breathlessness, dizziness or facial swelling during the infusion at once.
  • Mild flushing or muscle aches shortly after the dose can occur and usually settle.
  • A repeat course or oral iron may be needed once stores recover.

Evidence & guidelines

Intravenous iron is recommended where oral iron is poorly tolerated or ineffective, including in chronic kidney disease, per NICE guidance.

Reference: UK Renal Association Guidelines; SPC Venofer; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.