Venofer (Iron Sucrose) Dosing Guidelines
The recommended dosage of Venofer depends on the clinical indication: for hemodialysis-dependent chronic kidney disease (HDD-CKD), administer 100 mg undiluted as a slow IV injection over 2-5 minutes or as an infusion over at least 15 minutes per dialysis session; for non-dialysis dependent CKD (NDD-CKD), administer 200 mg over 2-5 minutes or as a 15-minute infusion on 5 occasions over 14 days; and for peritoneal dialysis-dependent CKD (PDD-CKD), give 300 mg twice (14 days apart) followed by 400 mg 14 days later. 1
Standard Adult Dosing by Clinical Setting
Hemodialysis-Dependent CKD (HDD-CKD)
- Dose: 100 mg per hemodialysis session 1
- Administration options:
- Timing: Administer early during dialysis session (generally within first hour) 1
- Total course: 1000 mg total treatment course; may repeat if iron deficiency recurs 1
Non-Dialysis Dependent CKD (NDD-CKD)
- Dose: 200 mg per administration 1
- Frequency: 5 doses over a 14-day period 1
- Administration options:
- Alternative regimen: 500 mg diluted in maximum 250 mL of 0.9% NaCl over 3.5-4 hours on Day 1 and Day 14 (limited experience) 1
Peritoneal Dialysis-Dependent CKD (PDD-CKD)
- Regimen: Three divided doses within 28 days 1:
- 300 mg over 1.5 hours (Day 1)
- 300 mg over 1.5 hours (Day 14)
- 400 mg over 2.5 hours (Day 28)
- Dilution: Maximum 250 mL of 0.9% NaCl 1
Pediatric Dosing (≥2 Years of Age)
HDD-CKD Maintenance Treatment
- Dose: 0.5 mg/kg (not to exceed 100 mg per dose) 1
- Frequency: Every 2 weeks for 12 weeks 1
- Administration: Undiluted over 5 minutes or diluted in 0.9% NaCl at 1-2 mg/mL over 5-60 minutes 1
NDD-CKD or PDD-CKD on Erythropoietin
- Dose: 0.5 mg/kg (not to exceed 100 mg per dose) 1
- Frequency: Every 4 weeks for 12 weeks 1
- Administration: Same as HDD-CKD pediatric dosing 1
Cancer-Related Anemia Dosing
For cancer patients with chemotherapy-induced anemia:
- Dose: 200 mg IV over 60 minutes 2
- Frequency: Repeated dosing every 2-3 weeks 2
- Maximum single dose: Individual doses above 300 mg are not recommended 2
- Maximum total dose: 1000 mg 2
Critical Safety Parameters
Maximum Dosing Limits
- Single dose maximum: 200 mg to minimize dose-related adverse effects 3, 4
- Weekly maximum: 500 mg 3, 4
- Typical administration: 100 mg per dose minimizes risk of arthralgia-myalgia reactions 3
Test Dose Requirements
- Not required for iron sucrose 2, 4
- Recommended for patients with history of sensitivities to IV iron preparations or multiple drug allergies 2, 4
- Test dose protocol (if used): 25 mg slow IV push, observe before proceeding 2
Absolute Contraindications
- Active bacteremia: Do not administer during active infection 2, 4
- Chronic infection alone is not an absolute contraindication if risk/benefit favors treatment 4
Administration Technique
Preparation
- Each mL contains 20 mg elemental iron 3, 1
- Available in 100 mg (5 mL) vials 3
- Dilute in normal saline solution for infusion 3
Infusion Monitoring
- Start infusion slowly for first 5 minutes to monitor for reactions 4
- Monitor vital signs during and after infusion 4
- Resuscitation facilities should be available 4
Managing Minor Infusion Reactions
- Stop the infusion immediately 4
- Switch to hydration fluid to keep vein open 4
- Monitor patient; most reactions are self-limiting and resolve spontaneously 4
- After 15 minutes, rechallenge may be considered with careful monitoring 4
- If symptoms persist or worsen after 15 minutes, consider IV hydrocortisone 4
Common Pitfalls to Avoid
- Do not exceed 200 mg single dose to minimize anaphylactoid reactions 4
- Avoid rapid administration of doses >100 mg; use appropriate infusion times 3, 1
- Do not dilute below 1 mg/mL concentration in pediatric patients 1
- Free iron may occur if 100 mg administered when transferrin <180 mg/dL 3
- Multiple visits required: Iron sucrose typically requires 4-7 visits for complete iron replenishment, unlike newer formulations 5
Monitoring Parameters
- Hemoglobin: Baseline and 3-4 weeks post-infusion 3
- Ferritin: Target ≥100 ng/mL 3
- Transferrin saturation: Target ≥20% 3
- Follow-up: 3-month intervals for first year 3
Adverse Effects Profile
- Incidence: Approximately 0.5% hypersensitivity-type and infusion reactions 4
- Common effects: Hypotension, nausea, vomiting, diarrhea 2, 4
- Rare effects: Hypotension, flushing, abdominal cramps (particularly with ACE inhibitors), arthralgias/myalgias 3
- Hypophosphatemia: Occurs in approximately 1% of patients (significantly lower than ferric carboxymaltose at 58%) 4