deferiprone
deferiprone
(de-fer-ip-rone) deferiprone,Ferriprox
(trade name)Classification
Therapeutic: antidotesPharmacologic: chelating agents
Indications
Action
Therapeutic effects
Pharmacokinetics
Time/action profile (blood levels)
ROUTE | ONSET | PEAK | DURATION |
---|---|---|---|
PO | within 5–10 min | 1–2 hr | 8–12 hr |
Contraindications/Precautions
Adverse Reactions/Side Effects
Central nervous system
- headache
Cardiovascular
- Torsades de Pointes (life-threatening)
Gastrointestinal
- abdominal pain (most frequent)
- nausea (most frequent)
- change in appetite
- vomiting
- ↑ liver enzymes
Genitourinary
- chromaturia (most frequent)
Hematologic
- agranulocytosis (life-threatening)
- neutropenia
Musculoskeletal
- arthralgia
- arthropathy
- back pain
- extremity pain
Miscellaneous
- ↓ zinc levels
Interactions
Drug-Drug interaction
Concurrent use of other drugs that cause neutropenia/agranulocytosis may ↑ risk of neutropenia/agranulocytosis. May also chelate other concurrently administered polyvalent cations in mineral supplements and antacids, including iron, aluminum and zinc ; wait 4 hr between administration.Route/Dosage
Availability
Nursing implications
Nursing assessment
- .
- Lab Test Considerations: Monitor serum ferritin every 2–3 mo to assess efficacy. If serum ferritin falls consistently below 500 mcg/L, consider temporarily interripting deferiprone therapy.
- Measure ANC before starting and weekly during therapy. Interrupt deferiprone if neutropenia (ANC <1.5 X 109/L) or if infection develops. If ANC <1.5 X 109/L and >0.5 X 109/L, obtain CBC with WBC corrected for presence of nucleated red blood cells, ANC, and platelet count daily until recovery (ANC ≥1.5 X 109/L. For agranulocytosis (ANC <0.5 X 109/L), Consider hospitalization and manage as clinically appropriate. Do not resume deferiprone in patients who develop agranulocytosis or rechallenge patients who develop neutropenia, unless benefits outweigh risks.
- Monitor serum AST and ALT monthly during therapy. Interrupt therapy if persistent ↑ in serum transaminases occurs.
- Monitor plasma zinc levels. ↓ may occur and may require supplementation.
Potential Nursing Diagnoses
Risk for infection (Adverse Reactions)Implementation
- Oral: Administer first dose in the morning, second dose midday, and third dose in the evening. May be taken with meals to decrease nausea.
Patient/Family Teaching
- Instruct patient to take deferiprone 3 times/day. Take missed doses as soon as remembered, but not just before next dose. Do not double doses.
- Advise patient to stop therapy and notify health care professional immediately if signs and symptoms of infection (fever, sore throat) or if palpitations, dizziness, syncope, or seizures occur.
- Inform patient that reddish/brown urine may occur; common and not harmful.
- Advise female patients to use contraception and avoid breastfeeding during therapy. If pregnancy is planned or suspected, notify health care professional promptly.
Evaluation/Desired Outcomes
- Decrease in serum ferritin levels.