Route of administration |
Subcutaneous or intravenous |
Oral |
Oral |
Half-life |
20 min |
2–3 h |
8–16 h |
Routes of iron excretion |
Urine/stool |
Urine |
stool |
Dose range |
20–60 mg/kg per day |
50–60 mg/kg per day |
20–30 mg/kg/day |
Guidelines for monitoring therapy |
Audiometry and eye exams annually |
Complete blood count weekly; ALT level monthly for first 3–6 months then every 6 months |
Serum creatinine level monthly; ALT level monthly |
Serum ferritin |
Serum ferritin |
Serum ferritin |
Assessment of liver iron annually |
Assessment of liver iron annually |
Assessment of liver iron annually |
Assessment of cardiac iron annually after 10 years of age |
Assessment of cardiac iron annually after 10 years of age |
Assessment of cardiac iron annually after 10 years of age |
Advantages |
Long-term experience |
Orally active |
Orally active |
Effective in maintaining normal or near-normal iron stores |
Safety profile well established |
Once-daily administration |
Reversal of cardiac disease with intensive therapy |
Enhanced removal of cardiac iron |
Demonstrated equivalency to deferoxamine at higher doses |
May be combined with deferiprone |
May be combined with deferoxamine |
Trials in several hematologic disorders |
Disadvantages |
Requires parenteral infusion |
May not achieve negative iron balance in all patients at 75 mg/kg per day |
Limited long-term data |
Ear, eye, bone toxicity |
Risk of agranulocytosis |
Need to monitor renal function |
Poor compliance |
|
May not achieve negative iron balance in all patients at highest dose |