Zyloprim reduces the production of uric acid in your body. Zyloprim
is used to treat gout, increased levels of uric acid caused by cancer
treatment, and kidney stones that are caused by high levels of uric
acid
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Allopurinol is a structural isomer of hypoxanthine (a naturally
occurring purine in the body) and acts to inhibit xanthine oxidase.
This enzyme is responsible for the successive oxidation of hypoxanthine
and xanthine resulting in the production of uric acid, the product
of human purine metabolism.[1] In addition to blocking uric acid
production, inhibition of xanthine oxidase causes an increase in
hypoxanthine and xanthine, which are converted to closely related
purine ribotides adenosine and guanosine monophosphates. Increased
levels of these ribotides causes feedback inhibition of amidophosphoribosyl
transferase, the first and rate-limiting enzyme of purine biosynthesis.
Allopurinol therefore decreases both uric acid formation and purine
synthesis
Allopurinol is in a class of medications called xanthine oxidase
inhibitors. It works by reducing the production of uric acid in
the body. High levels of uric acid may cause gout attacks or kidney
stones. Allopurinol is used to prevent gout attacks, not to treat
them once they occur.
Allopurinol is also sometimes used to treat seizures, pain caused
by pancreas disease, and certain infections. It is also sometimes
used to improve survival after bypass surgery, to reduce ulcer relapses,
and to prevent rejection of kidney transplants. Talk to your doctor
about the possible risks of using this medicine for your condition.The dosage of ZYLOPRIM to accomplish full control of gout and to lower serum uric acid to normal or near-normal levels varies with the severity of the disease. The average is 200 to 300 mg/day for patients with mild gout and 400 to 600 mg/day for those with moderately severe tophaceous gout. The appropriate dosage may be administered in divided doses or as a single equivalent dose with the 300 mg-tablet. Dosage requirements in excess of 300 mg should be administered in divided doses. The minimal effective dosage is 100 to 200 mg daily and the maximal recommended dosage is 800 mg daily.
Side effects of allopurinol are rare, though significant when they
occur. A small percentage of people develop a rash and must discontinue
this drug. The most serious adverse effect is a hypersensitivity
syndrome consisting of fever, skin rash, eosinophilia, hepatitis,
worsening renal function and, in some cases, allopurinol hypersensitivity
syndrome. Allopurinol is one of the drugs commonly known to cause
Stevens-Johnson syndrome (SJS), and Toxic Epidermal Necrolysis Syndrome
(TENS) which is an adverse drug reaction
Teratogenic Effects: Pregnancy Category C. Reproductive studies have been performed in rats and rabbits at doses up to twenty times the usual human dose (5 mg/kg per day), and it was concluded that there was no impaired fertility or harm to the fetus due to allopurinol. There is a published report of a study in pregnant mice given 50 or 100 mg/kg allopurinol intraperitoneally on gestation days 10 or 13. There were increased numbers of dead fetuses in dams given 100 mg/kg allopurinol but not in those given 50 mg/kg. There were increased numbers of external malformations in fetuses at both doses of allopurinol on gestation day 10 and increased numbers of skeletal malformations in fetuses at both doses on gestation day 13. It cannot be determined whether this represented a fetal effect or an effect secondary to maternal toxicity. There are, however, no adequate or well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.