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  • MADAUS Potassium Sodium Hydrogen Citrate Granules For Urinary Stones
  • MADAUS Potassium Sodium Hydrogen Citrate Granules For Urinary Stones
  • MADAUS Potassium Sodium Hydrogen Citrate Granules For Urinary Stones
  • MADAUS Potassium Sodium Hydrogen Citrate Granules For Urinary Stones

MADAUS Potassium Sodium Hydrogen Citrate Granules For Urinary Stones

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枸橼酸氢钠钾颗粒

Generic name: sodium potassium hydrogen citrate granules
Chinese Pinyin: ju yuan suan qing jia na ke li
English name: Potassium Sodium Hydrogen Citrate Granules
Product name: Friends of the special
Ingredients: The main ingredient of this product is potassium hydrogen citrate sodium.
Properties: Light orange particles, aromatic, salty.
Function and indication: Used to dissolve uric acid stones and prevent the formation of new stones, as a maintenance treatment for cystine stones and cystinuria.
Specification: 97.1g/100g/box
Usage and Dosage: Unless otherwise stated, the daily dose is 4 standard measuring spoons (each measuring spoon is 2.5g, a total of 10g granules). Take three times after meals, one measuring spoon each in the morning and noon, and two measuring spoons in the evening. Take it with water. The pH value of fresh urine must be within the following range: pH 6.2-6.8 for uric acid stones and uricosuric treatment; pH 7.0-8.0 for cystine stones; if the pH value is lower than the recommended range, the evening dose needs to be increased by measuring spoon, if the pH value If it is higher than the recommended range, it is necessary to reduce the measuring spoon by half in the evening. If the pH value of fresh urine measured before taking Youlaite remains within the recommended range, the patient and doctor can be sure that the appropriate dose has been found.
Adverse reactions: Slight stomach or abdominal pain can be seen. Occasionally, mild diarrhea and nausea occur.
Contraindications: Not to be used in patients with acute or chronic renal failure, or when sodium chloride is absolutely forbidden. Potassium sodium hydrogen citrate is also contraindicated in severe acid-base balance disorders (alkaline metabolism) or chronic urinary tract ureolytic bacteria infection.
Note: 1. Before taking this drug for the first time, measure serum electrolytes and check renal function. 2. When renal tubular acidosis (RTA) is suspected, the acid-base status should be checked. 3. Patients with severe liver dysfunction should use Uralyt-U with caution. 4. Please store the medicine out of reach of children.
Drug interactions: This medicine contains the coloring agent Orange S (E110), which may induce allergic reactions including asthma in susceptible persons. Allergic reactions are more likely to occur in patients taking 2-acetobenzoic acid (acetylsalicylic acid). Any increase in the concentration of extracellular potassium will reduce the heart's glucose metabolism, and any decrease in the concentration of extracellular potassium will increase the incidence of arrhythmia. Aldosterone antagonists, potassium-sparing diuretics, ACE inhibitors, non-steroidal anti-inflammatory drugs and peripheral analgesics can reduce renal potassium excretion. Please remember that 1g potassium hydrogen citrate sodium contains 0.172g or 4.4mmol potassium. If you require a low-sodium diet, remember that 1g of potassium hydrogen citrate sodium contains 0.1g or 4.4mmol sodium (equivalent to 0.26g sodium chloride).
Pharmacology and Toxicology: Oral use of YouLite increases urine PH value and citrate excretion, and reduces urine calcium ion concentration. This kind of change induced by Ulite uses the stone-forming salt in the urine to easily crystallize. The resulting decrease in calcium ion concentration can reduce the calcium salt saturation in urine that can form stones. An increase in pH can increase the solubility of uric acid and cystine stones.
Storage: After opening the medicine package, reseal the medicine for storage. If the medicine has been dissolved into water and prepared into a solution, it should be taken immediately.
Packing: 100g/tin, with test paper and measuring spoon.
Validity period: 60 months
Approval number: Imported drug registration number H20100795
Company name: MADAUS GmbH,Germany