Pajjiż: Awstralja
Lingwa: Ingliż
Sors: Department of Health (Therapeutic Goods Administration)
Allopurinol
Alphapharm Pty Ltd
Medicine Listed (Export Only)
PROGOUT _contains the active ingredient allopurinol_ CONSUMER MEDICINE INFORMATION WHAT IS IN THIS LEAFLET This leaflet answers some common questions about Progout. It does not contain all the available information. It does not take the place of talking to your doctor or pharmacist. All medicines have benefits and risks. Your doctor has weighed the risks of you taking Progout against the benefits expected for you or your child. IF YOU HAVE ANY CONCERNS ABOUT TAKING THIS MEDICINE, TALK TO YOUR DOCTOR OR PHARMACIST. KEEP THIS LEAFLET WITH YOUR MEDICINE. You may need to read it again. WHAT PROGOUT IS USED FOR Progout is used in the treatment of: • gouty arthritis or gout, a condition of painful swollen joints caused by uric acid crystals • kidney stones • other rare conditions where high levels of uric acid occur in the blood, for example Lesch-Nyhan syndrome. Progout helps to treat the symptoms of these conditions but will not cure them. It will not help treat the pain that occurs in an acute attack of gout. Progout belongs to a group of medicines called anti-uricaemic agents. These medicines reduce the amount of uric acid in the body. Most commonly, high levels of uric acid in the body are related to gout. Excess amounts of uric acid in the blood may lead to the development of crystals which deposit in the joints, causing pain, swelling and tenderness. ASK YOUR DOCTOR IF YOU HAVE ANY QUESTIONS ABOUT WHY PROGOUT HAS BEEN PRESCRIBED FOR YOU. Your doctor may have prescribed Progout for another reason. Progout is available only with a doctor's prescription. There is no evidence that Progout is addictive. BEFORE YOU TAKE PROGOUT _WHEN YOU MUST NOT TAKE IT_ DO NOT TAKE PROGOUT IF YOU ARE ALLERGIC TO MEDICINES CONTAINING ALLOPURINOL (E.G. ZYLOPRIM) OR ANY OF THE INGREDIENTS LISTED AT THE END OF THIS LEAFLET, INCLUDING LACTOSE. Some of the symptoms of an allergic reaction may include skin rash, itching or hives; swelling of the face, lips or tongue which may cause difficulty in swallowing or breathin Aqra d-dokument sħiħ
PROGOUT _Allopurinol _ PRODUCT INFORMATION NAME OF THE MEDICINE The active ingredient of Progout tablets is allopurinol. Chemical name: 1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one. Structural formula: Molecular formula: C 5 H 4 N 4 O Molecular weight: 136.1 CAS Registry no.: 315-30-0 DESCRIPTION Allopurinol is a white or off-white, almost odourless powder. It is very slightly soluble in water and in alcohol, and is practically insoluble in chloroform and in ether. It dissolves in dilute solutions of alkali hydroxides. Each Progout 100 tablet contains 100 mg of allopurinol. The tablets also contain the following inactive ingredients: lactose, starch - maize, povidone, macrogol 8000, sodium lauryl sulfate, talc - purified and magnesium stearate. The tablets are gluten free. Each Progout 300 tablet contains 300 mg of allopurinol. The tablets also contain the following inactive ingredients: starch - maize, povidone, maltodextrin, sodium starch glycollate, cellulose - microcrystalline and magnesium stearate. PHARMACOLOGY Allopurinol inhibits xanthine oxidase, the enzyme which catalyses the conversion of hypoxanthine to xanthine, and of xanthine to urate/uric acid. Allopurinol decreases urate formation in two ways: 1. The inhibition of xanthine oxidase reduces the amount of hypoxanthine and xanthine converted to urate/uric acid. 2. This action makes more hypoxanthine and xanthine available for re-utilisation in the purine metabolic cycle, which in turn, by a feedback mechanism, decreases overall _de novo_ purine formation. Since allopurinol decreases urate formation, it reduces urate/uric acid concentrations in both body fluids and urine. In contrast, the uricosuric agents which increase urate/uric acid excretion via the kidney will reduce the urate concentration in body fluids, but increase urate/uric acid concentrations in urine Aqra d-dokument sħiħ