What is the expected increase in iron levels after a single 200mg dose of Venofer (iron sucrose) IV?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: November 9, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Expected Increase in Iron Levels After a Single 200mg Venofer Dose

A single 200mg IV dose of Venofer (iron sucrose) will increase serum ferritin by approximately 288 ng/mL and hemoglobin by 0.9-1.4 g/dL over 4-6 weeks, with the magnitude of response depending on baseline iron stores. 1

Pharmacokinetic Profile

The iron component of Venofer exhibits first-order kinetics with an elimination half-life of 6 hours and distributes mainly in blood (steady-state volume of distribution 7.9 L), with significant amounts reaching the liver, spleen, and bone marrow. 2 Following IV administration, iron sucrose dissociates into iron and sucrose, with the iron transported as a complex with transferrin to erythroid precursor cells where it is incorporated into hemoglobin. 2

Expected Changes in Iron Parameters

Serum Ferritin Response

  • Patients receiving 5 weekly doses of 200mg (total 1000mg) showed a mean ferritin increase of 288 ng/mL compared to essentially no change (-5.1 ng/mL) with oral iron. 1
  • For a single 200mg dose, expect approximately one-fifth of this effect, or roughly 50-60 ng/mL increase in ferritin. 1

Hemoglobin Response

  • In CKD patients with baseline ferritin <100 ng/mL receiving 5 weekly 200mg doses, hemoglobin increased by 1.4 g/dL, compared to 0.9 g/dL with oral iron. 1
  • A single 200mg dose would contribute approximately 0.25-0.3 g/dL hemoglobin increase over several weeks. 3, 1

Transferrin Saturation

  • Significant increases in serum iron and decreases in total iron binding capacity occur within 4 weeks of initiating iron sucrose treatment at 100mg three times weekly. 2
  • A 200mg dose will acutely increase transferrin saturation, though the magnitude varies based on baseline transferrin levels. 4

Critical Timing Considerations for Accurate Assessment

You cannot accurately assess iron parameters immediately after a 200mg dose—wait at least 7 days before checking labs. 5 The guidelines specifically state that accurate assessment of iron parameters after IV infusion of 200-500mg may require an interval of 7 or more days. 5 This is because the iron initially enters an exchangeable compartment before being incorporated into storage and functional pools. 5

Factors Affecting Response Magnitude

Baseline Iron Status

  • Patients with lower baseline ferritin (<100 ng/mL) show greater hemoglobin responses to IV iron supplementation. 1
  • Free iron may occur if 100mg is administered when transferrin levels are less than 180 mg/dL, suggesting saturation of binding capacity. 4

Concurrent Erythropoietin Therapy

  • The combination of low-dose EPO with IV iron produces additive effects, with 80% of patients showing Hct increases ≥3% compared to 48.9% with iron alone. 3
  • Without EPO, one-third of predialysis CKD patients maintained target Hct with IV iron alone during maintenance therapy. 3

Clinical Efficacy Benchmarks

After 5 weekly doses of 200mg (1000mg total):

  • 54.2% of patients achieved hemoglobin >11.0 g/dL compared to 31.3% with oral iron. 1
  • 62.5% met combined hemoglobin/ferritin endpoints versus 0% with oral iron. 1
  • 43.8% met all three criteria (hemoglobin/ferritin/TSAT) versus 0% with oral iron. 1

Important Caveats

The 200mg dose represents the maximum single dose approved for iron sucrose, and doses larger than this are not recommended by guidelines. 5, 6 While the response to a single dose is modest, the cumulative effect of serial dosing produces clinically meaningful improvements in both iron stores and hemoglobin levels over 4-6 weeks. 3, 1

The actual clinical response depends heavily on ongoing iron losses (particularly in hemodialysis patients), baseline iron stores, concurrent EPO use, and underlying inflammatory states that may affect iron utilization. 3, 1

References

Guideline

Iron Sucrose Administration Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Iron Sucrose Administration Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.