Table 3.
| 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 |
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.