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allopurinol |
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allopurinol /al·lo·pur·i·nol/ (al″o-pūr´ĭ-nol) an isomer of hypoxanthine, capable of inhibiting xanthine oxidase and thus of reducing serum and urinary levels of uric acid; used in prophylaxis and treatment of hyperuricemia and uric acid nephropathy and prophylaxis of renal calculus recurrence.
Allopurinol A drug that corrects hyperuricemia by inhibiting urate production. Mentioned in: Gout allopurinol [al′əpyo̅o̅r′ənôl] a xanthine oxidase inhibitor uricosuric agent. indications It is prescribed in the treatment of gout and other hyperuricemic conditions. contraindications It is not prescribed for children (except those with hyperuricemia resulting from malignancy), lactating mothers, or people suffering an acute attack of gout. Known hypersensitivity to this drug prohibits its use. adverse effects Among the most serious adverse reactions are blood dyscrasias and severe rashes and other allergic reactions. GI and ophthalmologic disturbances also may occur. allopurinol (al´ n brand names: Lopurin, Zyloprim; drug class: antigout drug; action: inhibits the enzyme xanthine oxidase, reducing uric acid synthesis; uses: chronic gout, hyperuricemia associated with malignancies. allopurinol a drug that inhibits uric acid production and reduces serum and urinary uric acid levels; used in the treatment of urate uroliths in dogs. allopurinol Apo-Allopurinol (CA), Caplenol (UK), Cosuric (UK), Rimapurinol (UK), Zyloprim Pharmacologic class: Xanthine oxidase inhibitor Therapeutic class: Antigout drug Pregnancy risk category C ActionInhibits conversion of xanthine to uric acid and increases reutilization of hypoxanthine and xanthine for nucleic acid synthesis, thereby decreasing uric acid levels in both serum and urine AvailabilityPowder for injection: 500-mg vial Tablets: 100 mg, 300 mg ⊘Indications and dosages ➣ Gout in patients with frequent disabling attacks; gout resulting from hyperuricemia, acute or chronic leukemia, psoriasis, or multiple myeloma Adults: 200 to 300 mg P.O. daily in mild cases or 400 to 600 mg P.O. daily in severe cases, to a maximum dosage of 800 mg/day; or 200 to 400 mg/m2/day I.V. as a single infusion or in equally divided doses q 6, 8, or 12 hours Children ages 6 to 10: 300 mg P.O. daily Children younger than age 6: 150 mg P.O. daily ➣ To prevent acute gout attacks Adults: 100 mg P.O. daily; increase by 100 mg at weekly intervals without exceeding maximum dosage of 800 mg, until uric acid level falls to 6 mg/dl or less ➣ Recurrent calcium oxalate calculi Adults: 200 to 300 mg P.O. daily in single dose or divided doses ➣ To prevent uric acid nephropathy during cancer chemotherapy Adults: 600 to 800 mg P.O. daily for 2 to 3 days, accompanied by high fluid intake Dosage adjustment• Renal impairment Off-label uses• Hematemesis caused by gastritis induced by nonsteroidal anti-inflammatory drugs Contraindications• Hypersensitivity to drug PrecautionsUse cautiously in: Administration• Reconstitute single-dose vial with 25 ml sterile water for injection. Further dilute with normal saline solution or D5W to a concentration of 6 mg/ml or less.
Adverse reactionsCNS: drowsiness, dizziness, headache, peripheral neuropathy, neuritis, paresthesia CV: hypersensitivity vasculitis, necrotizing vasculitis EENT: retinopathy, cataract, epistaxis GI: nausea, vomiting, diarrhea, abdominal pain, dyspepsia, gastritis GU: exacerbation of gout and renal calculi, uremia, renal failure Hematologic: eosinophilia, anemia, thrombocytopenia, bone marrow depression, agranulocytosis, leukocytosis, aplastic anemia, leukopenia Hepatic: cholestatic jaundice, hepatomegaly, hepatitis, hepatic necrosis Musculoskeletal: myopathy, joint pain Skin: rash; alopecia; maculopapular, urticarial, or purpuric lesions; severe furunculosis of nose; ichthyosis; bruising; scaly or exfoliative erythema multiforme; toxic epidermal necrolysis Other: abnormal taste, loss of taste, fever, chills InteractionsDrug-drug. Amoxicillin, ampicillin, bacampicillin: increased risk of rash Anticoagulants (except warfarin): increased anticoagulant effect Antineoplastics: increased risk of myelosuppression Azathioprine, mercaptopurine: inhibition of allopurinol metabolism Chlorpropamide: increased hypoglycemic effects Diazoxide, diuretics, mecamylamine, pyrazinamide: increased uric acid levels Ethacrynic acid, thiazide diuretics: increased risk of allopurinol toxicity Uricosurics: increased uric acid excretion Urine-acidifying drugs (ammonium chloride, ascorbic acid, potassium or sodium phosphate): increased risk of renal calculi Xanthines: increased theophylline levels Drug-diagnostic tests. Alanine aminotransferase, alanine phosphatase, aspartate aminotransferase, bilirubin, eosinophils: increased levels Granulocytes, hemoglobin, platelets, white blood cells: decreased levels Drug-food. Caffeine-containing beverages and foods, mineral water, orange juice: decreased drug absorption, increased uric acid level Drug-behaviors. Alcohol use: increased uric acid level Patient monitoring• Assess fluid intake and output. Intake should be sufficient to yield daily output of at least 2 L of slightly alkaline urine. Patient teaching☞ Instruct patient to promptly report painful urination, bloody urine, rash, eye irritation, or swelling of lips and mouth. allopurinol Zyloprim® Therapeutics A xanthine oxidase inhibitor which lowers high uric acid and thus is effective for both 1º–eg gout and 2º–eg due to hematologic disorders or neoplasa–hyperuricemia
Pharmacology Allopurinol and its 1º metabolite, oxypurinol, inhibit xanthine oxidase; oral absorption; peak plasma at < 1 hr; T1⁄2 2-3 hrs Adverse effects Hypersensitivity reaction How to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit webmaster's page for free fun content. |
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