Common Intravenous Iron Formulations for Iron Deficiency
The most commonly used IV iron formulations are iron sucrose (Venofer), ferric carboxymaltose (Ferinject/Injectafer), ferric derisomaltose/iron isomaltoside 1000 (Monofer), ferric gluconate (Ferrlecit), and ferrumoxytol, with selection based on dosing convenience, safety profile, and clinical context. 1
Primary IV Iron Formulations
Iron Sucrose (Venofer)
- Maximum single dose is 200 mg, administered as an IV push over 10 minutes 1, 2
- Requires multiple doses (typically 5 rounds of 200 mg each over 14 days for a total of 1000 mg) to achieve full iron repletion 2, 3
- Large published trials in IBD patients demonstrate safety and efficacy 1
- No test dose required, unlike iron dextran preparations 1, 3
- Resuscitation facilities must be immediately available during all infusions 2
Ferric Carboxymaltose (Ferinject/Injectafer)
- Allows high single doses of 500-1000 mg (up to 20 mg/kg body weight) 1
- Can be delivered within 15 minutes, providing significant logistic advantage 1, 4
- Rapidly improves hemoglobin levels and replenishes depleted iron stores 4, 5
- Major caveat: Associated with hypophosphatemia in 50-74% of patients due to elevated FGF-23, which can cause bone pain, osteomalacia, and fractures with repeated use 6, 7, 8
- Hypophosphatemia severity correlates with FCM dose and may persist for 6 months 8
Ferric Derisomaltose/Iron Isomaltoside 1000 (Monofer)
- Allows complete iron repletion in a single infusion with doses up to 20 mg/kg 9
- Significantly lower risk of hypophosphatemia compared to ferric carboxymaltose, making it a safer option for repeated dosing 9, 6
- Administered as an IV infusion over 15-30 minutes 9
- No test dose required 9
- Large published trials in IBD patients demonstrate efficacy 1
Ferric Gluconate (Ferrlecit)
- Maximum single dose is 125 mg of elemental iron 10
- Typically administered over 60 minutes for the 125 mg dose 10
- Terminal elimination half-life approximately 1-1.5 hours 10
- Contains benzyl alcohol (9 mg/mL) as inactive ingredient 10
- Commonly used in hemodialysis patients at 100-200 mg per dialysis session 10
Ferrumoxytol
- Licensed for use in chronic kidney disease 1
- Currently undergoing Phase III trials in IBD and other conditions associated with iron deficiency 1
- Small data series available but less extensively studied than other formulations 1
Formulations to Avoid
Iron Dextran
- Requires mandatory test dose due to risk of serious anaphylactic reactions (0.6-0.7% incidence) 1
- 31 fatalities reported between 1976 and 1996 1
- Can deliver up to 20 mg/kg in single infusion over 6 hours, but safety concerns limit use 1
- Modern non-dextran formulations are strongly preferred 1, 5
Intramuscular Iron
- Obsolete and should not be used—injections are painful, damaging to tissues, and associated with unacceptable side effects 1
Practical Selection Algorithm
For patients requiring rapid, complete iron repletion in single infusion:
- Choose ferric derisomaltose (preferred due to lower hypophosphatemia risk) 9, 6
- Alternative: ferric carboxymaltose if ferric derisomaltose unavailable, but monitor phosphate levels 1, 6
For patients with inflammatory bowel disease or active inflammation:
- IV iron is first-line over oral iron 1
- Iron sucrose, ferric carboxymaltose, or ferric derisomaltose all have large published trials demonstrating efficacy 1
For hemodialysis patients:
- Iron sucrose 100-200 mg or ferric gluconate 125 mg administered 2-3 times weekly into dialysis line 3, 10
For patients requiring multiple smaller doses:
Critical Safety Considerations
- All IV iron formulations carry risk of severe infusion reactions (<1% in prospective trials), requiring immediate availability of resuscitation equipment 1, 6, 7
- Hypersensitivity reactions are usually non-allergic Complement Activation-Related Pseudo-Allergy (CARPA), reduced by slow infusion rates 6
- Avoid exceeding transferrin saturation >50% or ferritin >800 μg/L to prevent iron overload 1
- Never administer IV iron during active bacterial infection 3
- With ferric carboxymaltose, monitor serum phosphate at baseline and post-treatment due to high hypophosphatemia risk 6, 7, 8