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. 2014 Dec 11;8:2475–2491. doi: 10.2147/DDDT.S55499

Table 1.

Pharmacologic characteristics of the main intravenous iron complexes

Sodium ferric gluconate complexa Iron sucroseb High molecular weight iron dextranc Low molecular weight iron dextrand Ferric carboxymaltosee Ferumoxytolf Isomaltoside 1,000g
Trade name Ferrlicit® Venofer® Dexferrum® Cosmoser®
INFeD®
Ferinject® FeraHeme® Monofer®
Carbohydrate shell Gluconate Sucrose Dextran (branched polysaccharide) Dextran (branched polysaccharide) Carboxymaltose (branched polysaccharide) Polyglucose sorbitol carboxymethylether Isomaltoside 1,000 (linear oligosaccharide)
Molecular weight (Da)# 37,500 34,000–60,000 265,000 165,000 150,000 750,000 150,000
Classificationh Type III Type II Type I Type I Type I Type I Type I
Iron content (mg/mL) 12.5 20 50 50 50 30 100
Half-life (hours) 1 6 9–87 5–20 7–12 15 20
Maximum single dose (mg) 125 200 20 mg/kg 20 mg/kg 15 mg/kg (max 1,000 mg)* 510 20 mg/kg
Reactivity with transferrin High Medium Low Low Low Low Low
Test dose required## No No Yes Yes No No No

Notes:

a

Ferrlecit® prescribing information. Sanofi Aventis, Inc Bridgewater, NJ, USA.

b

Venofer® prescribing information. Vifor Pharma Ltd Glattbrugg, Switzerland.

c

Dexferrum® INFeD® prescribing information, Pharma, Morristown, NJ, USA.

d

Cosmofer® prescribing information, Pharmacosmos A/S, Holbæk, Denmark.

e

Ferinject® Injectafer® prescribing information. Vifor Pharma Ltd Glattbrugg, Switzerland.

f

Feraheme® prescribing information. AMAG Pharmaceuticals, Inc Waltham, MA, USA.

g

Monofer® prescribing information. Pharmacosmos A/S, Holbæk, Denmark.

h

Type I complexes are robust and strong and thus release only minimal amounts of ionic iron in the blood stream. Type II complexes are semi-robust and moderately strong and consequently less stable than Type I complexes. Type III complexes are the least stable and therefore release relatively large amounts of ionic iron into the blood stream. Type IV complexes are mixed complexes. They are heterogeneous mixtures, which may induce side effects such as allergic responses and saturation of the iron transport system.22

#

The molecular weight in this table are those given by the manufacturer, but since they are measured with different standards the values are not totally comparable.

##

This is only the case in USA. In Europe, the test dose has been removed for all iv iron products.

*

for infusion the maximal iron dose is 20 mg/mL.