Therapeutic Classification: antigout agents, antihyperuricemics
Pharmacologic Classification: xanthine oxidase inhibitors
REMS
Absorption: Well absorbed (80%) following oral administration.
Distribution: Widely distributed in tissue and breast milk.
Protein Binding: <1%.
Half-Life: 13 hr (oxypurinol 1830 hr).
(hypouricemic effect)
ROUTE | ONSET | PEAK | DURATION |
---|---|---|---|
PO, IV | 12 days | 12 wk | 13 wk‡ |
‡Duration after discontinuation of allopurinol.
Contraindicated in:
Use Cautiously in:
CV: bradycardia, flushing, heart failure (reported with IV administration), hypertension, hypotension
Derm: rash (discontinue drug at first sign of rash), DRUG REACTION WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS (DRESS), STEVENS-JOHNSON SYNDROME, TOXIC EPIDERMAL NECROLYSIS, urticaria
GI: diarrhea, hepatitis, nausea, vomiting
GU: hematuria, renal failure
Hemat: bone marrow depression
Neuro: drowsiness
Drug-drug:
Gout
Renal Impairment
Secondary Hyperuricemia
Renal Impairment
Lab Test Considerations:
IV Administration:
NDC Code