URAL EFFERVESCENT POWDER SACHET 28

AUST R 296693

Sold by Calmans Pharmacy / Approval # 14510Q

URAL 
 
 
COMPOSITION 
 
Each 4 g contains Sodium Bicarbonate 1.76 g, Anhydrous Sodium Citrate 0.63 g, 
Anhydrous Citric Acid 0.72 g, Tartaric Acid 0.89 g. 
 
Also contains Nature Identical Lemon Flavour Oil, Terpeneless and Saccharin Sodium. 
 
 
ACTIONS 
 
Urinary and gastric alkaliniser 
 
 
INDICATIONS 
 
Urinary alkalinisation where indicated in the treatment of urinary tract infection; 
symptomatic relief of dysuria; to enhance the action of certain antibiotics, especially 
some sulphonamides, streptomycin, kanamycin, gentamicin; in gout especially when 
treated with uricosurics, and possibly allopurinol; symptomatic treatment of gastric 
hyperacidity. 
 
 
CONTRA-INDICATIONS 
 
Renal failure or hypernatraemia; in conjunction with hexamine mandelate or hexamine 
hippurate therapy because an acid urine is needed. 
 
Caution is advised in overt and occult cardiac failure. Concomitant use of urinary 
alkalinisers and quinolone antibiotics should be avoided; crystalluria may be more likely 
to occur in alkaline urine. 
 
 
PRECAUTIONS 
 
This preparation contains 644 mg of sodium per sachet which should be taken into 
account by those on a low sodium diet. 
 
Ural should be used cautiously in patients with cardiac failure, hypertension, impaired 
renal function, peripheral and pulmonary edema and preeclampsia. 
 URAL- Product Information Page 2 of 3
The clinical condition of the patient should be evaluated and laboratory determinations 
(eg. serum electrolytes, acid-base balance) obtained periodically during Ural therapy, 
particularly in patients with renal disease. 
 
 
DRUG INTERACTIONS 
 
General: Alkalisation of the urine due to the use of Ural, theoretically, may result in a 
decreased therapeutic effect of the following medications: chlorpropamide, lithium, 
salicylates and tetracyclines. Alternatively, alkalisation of the urine due to the use of 
Ural, theoretically, may result in an increased therapeutic effect of the following 
medications: amphetamines, ephedrine/pseudoephedrine. 
 
Antacids: Concurrent use of antacids with citrates may result in systemic alkalosis. 
Concomitant administration of antacids with sodium citrate and sodium bicarbonate may 
promote the development of calcium stones in patients with uric acid stones and may also 
cause hypernatremia. Concurrent use of aluminium-containing antacids with citrate salts 
can increase aluminium absorption, possibly resulting in acute aluminium toxicity, 
especially in patients with renal insufficiency. 
 
Quinolones: Citrates may reduce the solubility of ciprofloxacin, norfloxacin or ofloxacin 
in the urine. Patients should be observed for signs of crystalluria and nephrotoxicity. 
 
Laxatives: Concurrent administration of citrates with laxatives may have an additive 
effect. 
 
Pregnancy: 
Studies regarding the effect of citrates on pregnancy have not been done. 
 
Nursing Mothers: 
Caution should be exercised when administered to a nursing mother. 
 
 
ADVERSE REACTIONS 
 
The tartrate component of Ural may be incompletely absorbed. Because of this Ural may 
exert a mild laxative effect. Prolonged and excessive use may cause a systemic alkalosis 
and/or hypernatraemia. 
 
 
DOSAGE AND ADMINISTRATION 
 
4 g to 8 g (1 to 2 sachets) dissolved in cold water four times daily or as prescribed. 
 
 
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PACK 
 
Effervescent granules, 28 x 4 g sachets per pack

THIS MEDICINE MAY NOT BE RIGHT FOR YOU, READ THE WARNINGS BEFORE PURCHASE
IF SYMPTOMS PERSIST, TALK TO YOUR HEALTHCARE PROFESSIONAL





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