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Related to Aloprim: allopurinol, colchicine, Lopurin


a drug that inhibits uric acid production and reduces serum and urinary uric acid levels; used for treatment of hyperuricemia of gout and prophylaxis and treatment of hyperuricemia secondary to blood dyscrasias or cancer chemotherapy and of uric acid nephropathy, as well as for prophylaxis of kidney stone formation.
Miller-Keane Encyclopedia and Dictionary of Medicine, Nursing, and Allied Health, Seventh Edition. © 2003 by Saunders, an imprint of Elsevier, Inc. All rights reserved.


Apo-Allopurinol (CA), Caplenol (UK), Cosuric (UK), Nu-purol (CA), Rimapurinol (UK), Zyloprim, Zyloprim (CA)

allopurinol sodium


Pharmacologic class: Xanthine oxidase inhibitor

Therapeutic class: Antigout drug

Pregnancy risk category C


Inhibits 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


Powder 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 to a maximum dosage of 600 mg/day

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

• Pain from acute pancreatitis

• Seizures refractory to standard therapy


• Hypersensitivity to drug


Use cautiously in:

• acute gout attack, renal insufficiency, dehydration

• pregnant or breastfeeding patients.


• 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.

• Infuse over 30 to 60 minutes.

• Don't mix I.V. form with other drugs or give through same I.V. port as drugs that may be incompatible.

• Divide oral doses larger than 300 mg.

• Give oral form with or right after meals.

• Don't give oral form with mineral water, orange juice, or caffeinated beverages.

Adverse reactions

CNS: 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


Drug-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.

• Monitor uric acid level to help evaluate drug efficacy.

Patient teaching

Instruct patient to promptly report painful urination, bloody urine, rash, eye irritation, or swelling of lips and mouth.

• Tell patient to take drug with food or milk, exactly as prescribed.

• Explain that gout attacks may not ease significantly until 2 to 6 weeks of therapy.

• Caution patient to avoid driving and other hazardous tasks until he knows how drug affects concentration and alertness.

• Advise patient to avoid alcohol, caffeine-containing beverages and foods, mineral water, and orange juice during therapy.

• As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the drugs, tests, foods, and behaviors mentioned above.

McGraw-Hill Nurse's Drug Handbook, 7th Ed. Copyright © 2013 by The McGraw-Hill Companies, Inc. All rights reserved


Inhibitor of xanthine oxidase to inhibit uric acid formation; used in the treatment of gout and to retard the rapid metabolic degradation of 6-mercaptopurine.
Farlex Partner Medical Dictionary © Farlex 2012


(ăl′ō-pyo͝or′ə-nôl′, -nōl′, -nŏl′)
A drug, C5H4N4O, that inhibits uric acid formation in the body and is used to treat conditions, especially gout, that cause elevated uric acid levels.
The American Heritage® Medical Dictionary Copyright © 2007, 2004 by Houghton Mifflin Company. Published by Houghton Mifflin Company. All rights reserved.


A xanthine oxidase inhibitor which lowers high uric acid and thus is effective for both primary (e.g., gout) and secondary­ (e.g., due to hematologic disorders or neoplasa) hyperuricemia.
Allopurinol and its primary metabolite, oxypurinol, inhibit xanthine oxidase; oral absorption; peak plasma at < 1 hour; T1⁄2 2–3 hours.
Adverse effects
Hypersensitivity reaction.
Segen's Medical Dictionary. © 2012 Farlex, Inc. All rights reserved.


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
McGraw-Hill Concise Dictionary of Modern Medicine. © 2002 by The McGraw-Hill Companies, Inc.


A drug used to treat gout. Allopurinol is a xanthine oxidase inhibitor which reduces the production of uric acid from nucleic acid breakdown. The drug is on the WHO official list. A brand name is Zyloric.
Collins Dictionary of Medicine © Robert M. Youngson 2004, 2005


A drug that corrects hyperuricemia by inhibiting urate production.
Mentioned in: Gout
Gale Encyclopedia of Medicine. Copyright 2008 The Gale Group, Inc. All rights reserved.


Inhibitor of xanthine oxidase to inhibit uric acid formation; used treat gout and retard rapid metabolic degradation of 6-mercaptopurine.
Medical Dictionary for the Dental Professions © Farlex 2012