Table III.
CHELATOR AND ROUTE OF ADMINISTRATION | TOXICITIES | MONITORING RECOMMENDATIONS |
---|---|---|
Deferoxamine | Reduced visual acuity | Annual Eye exam |
Impaired color vision | Annual Hearing exam | |
Subcutaneous or parenteral infusion | Abnormal visual evoked potentials | Annual zinc level |
Night blindness | ||
Lens opacities | ||
High frequency sensorineural hearing loss | ||
Tinnitus | ||
Growth retardation | ||
Genu valgum | ||
Zinc deficiency | ||
Deferasirox | Gastrointestinal toxicity: nausea, vomiting, diarrhea, abdominal pain | LFTs every 2 weeks, at one month, then monthly |
Oral | Renal function and urinalysis monthly | |
Increased creatinine | ||
Proteinuria | CBC with differential every 3 months | |
Increased ALT | ||
Consider annual eye exam | ||
Consider annual hearing exam | ||
Deferiprone | Neutropenia / Agranulocytosis | CBC with differential weekly* |
Consider annual eye exam | ||
Oral | Consider annual hearing exam |
In the US, deferiprone is subject to a Risk Evaluation and Management system (REMS) and limited distribution; both patients and prescribers must sign to the effect that they understand the importance of monitoring weekly CBCs.