BOXED WARNING Agranulocytosis and neutropenia; measure ANC before and monitor regularly during therapy; interrupt if neutropenia/infection develops.
FDA dosing
Population
Start
Target
Max
Transfusional iron overload — FERRIPROX Tablets (twice a day), 1,000 mg
Adults & peds ≥8 yr
75 mg/kg/day in 2 divided doses (~12 h apart) with food
Adjust to response/iron burden
99 mg/kg/day in 2 divided doses
Transfusional iron overload — FERRIPROX Tablets (three times a day), 1,000 mg
Adults & peds ≥8 yr
75 mg/kg/day in 3 divided doses
Adjust to response/iron burden
99 mg/kg/day in 3 divided doses
Renal Undefined
Hepatic Undefined
Instructions
Two distinct 1,000 mg tablets: twice-a-day tablet (2 doses ~12 h apart, with food) vs three-times-a-day tablet (3 doses) — identify formulation before dispensing; schedules not interchangeable. Round total daily dose to nearest 500 mg (half-tablet).
Monitor ANC before therapy, then weekly (first 6 mo), every 2 weeks (next 6 mo), every 2-4 weeks thereafter.
For patients with difficulty swallowing, consider oral solution.
Available strengths
tab 500, 1000 mg
sol 100 mg/mL
Cautions
Agranulocytosis and neutropenia — can be fatal
Liver enzyme (ALT) elevations
Zinc deficiency
Hypersensitivity (Henoch-Schonlein purpura, urticaria, periorbital edema with rash)
Adverse reactions
Nausea
Vomiting
Abdominal pain
Arthralgia
ALT increased
Neutropenia
Pregnancy Animal structural abnormalities, embryo-fetal mortality; limited human data insufficient.
Lactation Breastfeeding not recommended during and for >=2 weeks after last dose.
NADAC is a voluntary CMS survey of what retail community pharmacies pay for the drugs they stock. Deferiprone is dispensed outside retail pharmacies, so it rarely appears on surveyed invoices.