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Allopurinol Tablets

Function and Efficacy

This product is a drug that inhibits the synthesis of uric acid. Allopurinol and its metabolite oxypurinol can inhibit xanthine oxidase, prevent hypoxanthine and xanthine from being metabolized into uric acid, and thus reduce the production of uric acid. It reduces the uric acid content in blood and urine to a level below the solubility, prevents uric acid from forming crystals and depositing in joints and other tissues, and also helps to redissolve uric acid crystals in the tissues of gout patients. Allopurinol also inhibits the synthesis of new purines in the body by acting on hypoxanthine-guanine phosphate nucleic acid transferase. The blood uric acid concentration of this product begins to decrease 24 hours after oral administration, and the decrease is most obvious in 2 to 4 weeks. Acute toxicity test results: The oral LD50 of rats is 6000 mg/kg, and the intraperitoneal injection LD50 is 750 mg/kg; the oral LD50 of mice is 700 mg/kg, and the intraperitoneal injection LD50 is 160 mg/kg.

Ingredients

Allopurinol. Its chemical name is 1H-pyrazolo[3,4-d]pyrimidin-4-ol. Its structural formula is: Molecular formula: C5H4N4O Molecular weight: 136.11

Name Description Content CAS NO. Manufacturer
AllopurinolIngredients

This product is a drug that inhibits the synthesis of uric acid. Allopurinol and its metabolite oxypurinol can inhibit xanthine oxidase, preventing hypoxanthine and xanthine from being metabolized into uric acid, thereby reducing the production of uric acid. It reduces the uric acid content in the blood and urine to a level below the solubility, prevents uric acid from forming crystals and depositing in joints and other tissues, and also helps to redissolve uric acid crystals in the tissues of gout patients. Allopurinol also inhibits the synthesis of new purines in the body by acting on hypoxanthine-guanine phosphate nucleic acid convertase.

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Appearance

This medicine is a white tablet.

Indication

It is used for ① primary and secondary hyperuricemia, especially hyperuricemia caused by excessive uric acid production; ② recurrent or chronic gout; ③ tophi; ④ uric acid kidney stones and (or) uric acid nephropathy; ⑤ hyperuricemia with renal insufficiency.

Usage and Dosage

Oral: 1 Common dosage for adults: Initial dose is 50 mg once, 1 to 2 times a day, and can be increased by 50 to 100 mg per week to 200 to 300 mg per day, divided into 2 to 3 doses. Measure blood and urine uric acid levels every 2 weeks. If they have reached normal levels, no more increments will be made. If they are still high, they can be increased again. However, the maximum daily dose should not exceed 600 mg. 2 Common dosage for children to treat secondary hyperuricemia: 50 mg each time for children under 6 years old, 1 to 3 times a day; 100 mg each time for children aged 6 to 10 years old, 1 to 3 times a day. The dosage can be adjusted as appropriate.

Adverse Reactions

1. Rash: It may be pruritic papules or urticaria. If the rash is widespread and persistent, symptomatic treatment is ineffective, and there is a tendency to worsen, the drug must be discontinued; 2. Gastrointestinal reactions: including diarrhea, nausea, vomiting and abdominal pain; 3. Leukopenia, thrombocytopenia, anemia, or bone marrow suppression should all be considered for discontinuation of the drug; 4. Other symptoms include hair loss, fever, lymphadenopathy, hepatotoxicity, interstitial nephritis and allergic vasculitis; 5. Several cases of sudden death of patients with unknown causes while taking this product have been reported abroad.

Precautions

It is contraindicated for patients who are allergic to this product, have severe liver and kidney dysfunction, or have obvious low blood cells.

Special Population Medication

Precautions for children: The dosage for children should be adjusted as appropriate. Precautions for pregnancy and lactation: Forbidden. Precautions for the elderly: The elderly should use the drug with caution and reduce the daily dosage.

Drug Interactions

1. Drinking alcohol, chlorthalidone, ethacrynic acid, furosemide, metolazone, pyrazinamide or thiazide diuretics can increase the uric acid content in serum. When using this product to control gout and hyperuricemia, attention should be paid to the adjustment of the dosage. For patients with hypertension or poor renal function, there are reports of renal failure and allergies when this product is used together with thiazide diuretics. 2. When this product is used together with ampicillin, the incidence of rash increases, especially in patients with hyperuricemia. 3. When this product is used together with anticoagulants such as dicoumarol and indandione derivatives, the effect of anticoagulants can be enhanced, and attention should be paid to adjusting the dosage. 4. When this product is used together with azathioprine or mercaptopurine, the dosage of the latter should generally be reduced by 1/4 to 1/3. 5. When this product is used together with cyclophosphamide, the suppression of bone marrow can be more obvious. 6. When this product is used together with uricosuric drugs, the possibility of kidney stone formation can be increased.

Storage

Keep away from light and sealed, valid for three years.

Packaging Specification

0.1g

Validity Period

36 months

Manufacturer

Beijing Yongkang Pharmaceutical Co., Ltd.

  • Founded in:

    1980-06-18
  • Address:

    No. 2, Section 3, Guba Road, Chengguan Street, Fangshan District, Beijing
  • Tax NO.:

    91110106802219135P
  • Registered Funds:

    20 million yuan
  • Website:

  • Email:

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