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. 2015 Aug 15;6(3):62–72. doi: 10.4291/wjgp.v6.i3.62

Table 3.

Available preparations for intravenous iron supplementation[16,24,26]

Iron dextran (LMW) Iron gluconate Iron sucrose Ferric carboxymaltose Ferumoxytol Iron isomaltoside
Product/Europe Product/United States CosmoFer® INFeD® Ferrlecit® Ferrlecit® Venofer® Venofer® Ferinject® Injectafer® Rienso® Feraheme® Monofer® Not available in United States
Manufacturer Pharmacosmos Sanofi-Aventis Vifor Vifor AMAG Pharmacosmos
Test dose required Yes No Yes (in Europe)/No No No No
Maximum approved dose 20 mg/kg 125 mg 200 mg (500 mg in few countries) 7 mg/kg Ferinject- 1000 mg, or up to maximum of 20 mg/kg Injectafer-1500 mg if patient’s weight > 50 kg 15 mg/kg if < 50 kg 1020 mg 20 mg/kg
Iron dextran (LMW) Iron gluconate Iron sucrose Ferric carboxymaltose Ferumoxytol Iron isomaltoside
Maximum injectable single dose 100 mg (2 mL) 125 mg (10 mL) 200 mg (10 mL) Ferinject- 1000 mg or up to maximum of 20 mg/kg Injectafer- 750 mg (15 mL) 510 mg (17 mL) 200 mg (2 mL)
Maximum infusion time 360 min (6 h) 30-60 min 210 min (3.5 h) 15 min 15 min 15 min
Maximum injection time 2 min 10 min 5-10 min Bolus push over 7.5 min 17 s (1 mL/s) Bolus push
Dose-related reactions Dextran induced IgE -mediated anaphylaxis, hypotension, edema Hypotension, edema Hypotension, edema None reported None reported None reported
Relative risk of adverse side effects Moderate Low Very low None reported Very low None reported
Costs per 500 mg in €1 Costs per maximum single injectable dose in United States dollars 84-86 € $37.70 52-56 € $76.32 105-100 € $120 170-175 € $993.75 82.12 $658.54 170-175 € Not available
FDA Pregnancy category INFeD-category C Cosmofer - no data available B B C C Can be used in 2nd and 3rd trimester
Additional comments FDA approved for IDA in CKD receiving hemodialysis and supplemental epoetin therapy FDA approved for IDA in CKD patients Has been studied in patients with IDA associated with CKD either dialysis and nondialysis dependant, IBD, CHF, post-partum and pregnancy patients. Transient hypophosphatemia has been reported FDA approved for IDA in CKD patients May transiently interfere with “tissue” diagnostic ability of MRI for up to 3 mo and “vascular” MRI for up to 2 d Very low immunogenic potential
1

In Germany August 2012. Prescribing information of marketed products, package inserts. LMW: Low molecular weight; CKD: Chronic kidney disease; CHF: Congestive heart failure; IDA: Iron deficiency anemia; IBD: Inflammatory bowel disease.