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Pronunciation |
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(sul
fin PEER a
zone) |
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U.S. Brand
Names |
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Anturane® |
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Generic
Available |
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Yes |
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Canadian Brand
Names |
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Antazone®; Anturan®;
Apo®-Sulfinpyrazone; Novo-Pyrazone; Nu-Sulfinpyrazone |
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Pharmacological Index |
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Uricosuric Agent |
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Use |
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Treatment of chronic gouty arthritis and intermittent gouty arthritis
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Pregnancy Risk
Factor |
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C; D (near term, per expert analysis) |
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Contraindications |
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Active peptic ulcers, hypersensitivity to sulfinpyrazone, phenylbutazone, or
other pyrazoles, GI inflammation, blood dyscrasias |
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Warnings/Precautions |
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Safety and efficacy not established in children <18 years of age, use with
caution in patients with impaired renal function and
urolithiasis |
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Adverse
Reactions |
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1% to 10%: Gastrointestinal: Nausea, vomiting, stomach pain
<1%:
Cardiovascular: Flushing
Central nervous system: Dizziness, headache
Dermatologic: Dermatitis, rash
Hematologic: Anemia, leukopenia, increased bleeding time (decreased platelet
aggregation)
Hepatic: Hepatic necrosis
Genitourinary: Polyuria
Renal: Nephrotic syndrome, uric acid stones |
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Overdosage/Toxicology |
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Symptoms of overdose include nausea, vomiting, ataxia, respiratory
depression, seizures
Following GI decontamination, treatment is supportive only
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Drug
Interactions |
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CYP2C and 3A3/4 enzyme inducer; CYP2C9 enzyme inhibitor
Increased effect of oral anticoagulants
Risk of acetaminophen hepatotoxicity is increased, but therapeutic effects
may be reduced |
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Mechanism of
Action |
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Acts by increasing the urinary excretion of uric acid, thereby decreasing
blood urate levels; this effect is therapeutically useful in treating patients
with acute intermittent gout, chronic tophaceous gout, and acts to promote
resorption of tophi; also has antithrombic and platelet inhibitory
effects |
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Pharmacodynamics/Kinetics |
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Absorption: Complete and rapid
Metabolism: Hepatic to two active metabolites
Half-life, elimination: 2.7-6 hours
Time to peak serum concentration: 1.6 hours
Elimination: Renal excretion with 22% to 50% as unchanged drug
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Usual Dosage |
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Adults: Oral: 100-200 mg twice daily; maximum daily dose: 800 mg
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Dietary
Considerations |
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Should be administered with food or milk |
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Monitoring
Parameters |
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Serum and urinary uric acid, CBC |
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Test
Interactions |
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uric acid
(S) |
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Mental Health: Effects
on Mental Status |
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May cause dizziness |
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Mental Health:
Effects on Psychiatric
Treatment |
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May cause leukopenia; use caution with clozapine and
carbamazepine |
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Dental Health: Local
Anesthetic/Vasoconstrictor
Precautions |
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No information available to require special precautions |
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Dental Health:
Effects on Dental Treatment |
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No effects or complications reported |
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Patient
Information |
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Take as directed, with meals or antacids and a full glass of water. Avoid
aspirin or acetaminophen products and avoid large quantities of vitamin C. It is
very important to maintain adequate hydration (2-3 L/day of fluids unless
instructed to restrict fluid intake) to prevent kidney damage. You may
experience nausea or vomiting (small frequent meals, frequent mouth care,
chewing gum, or sucking lozenges may help). Report skin rash, persistent stomach
pain, painful urination or bloody urine, unusual bruising or bleeding, fatigue,
or yellowing of eyes or skin. Pregnancy/breast-feeding precautions:
Inform prescriber if you are or intend to be pregnant. Consult prescriber if
breast-feeding. |
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Nursing
Implications |
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Monitor serum and urinary uric acid |
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Dosage Forms |
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Capsule: 200 mg
Tablet: 100 mg |
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References |
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Emmerson BT, "The Management of Gout," N Engl J Med, 1996,
334(7):445-51. |
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