Kataria granules 4 g sachet 5.6 g #6

Instructions for Kataria granules 4 g sachet 5.6 g No. 6

Composition

active ingredient: sodium citrate;

1 sachet (5.6 g of granules) contains 4 g of sodium citrate;

excipients: sucrose, sodium saccharin, cranberry flavoring 191121.

Dosage form

Granules.

Main physicochemical properties: white or almost white free-flowing granules with a pleasant odor.

Pharmacotherapeutic group

Drugs used in urology. ATX code G04B X.

Pharmacological properties

Pharmacodynamics

Sodium citrate is metabolized into bicarbonate, which contributes to the regression of dysuria observed in cystitis, reduces the acidity of urine, causing alkalization.

Pharmacokinetics

The pharmacokinetics of sodium citrate correspond to its natural pharmacokinetics in the body.

Indication

Relieving symptoms of cystitis in women.

Contraindication

Hypersensitivity to the active substance or to other components of the drug; diabetes; heart disease; arterial hypertension; kidney disease; being on a low-salt diet; pregnancy, breastfeeding.

Interaction with other medicinal products and other types of interactions

Concomitant use of sodium-containing drugs should be avoided in patients receiving lithium preparations, as sodium is predominantly absorbed by the kidneys, leading to increased lithium excretion and a decrease in its plasma levels.

Drugs that promote urine alkalization, in particular sodium citrate, should not be used simultaneously with urotropin, as it is only effective in acidic urine.

The therapeutic effect of a number of drugs may be reduced or increased by alkalinization of urine or lowering of the pH of gastric juice, which occur as a result of the action of sodium citrate.

Application features

If symptoms persist after two days of treatment, consult a doctor. Do not exceed the recommended dose.

Excipients: This medicinal product contains sucrose. If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.

This medicinal product contains 40.8 mmol (939 mg) sodium/dose. Caution should be exercised when administered to patients on a controlled sodium diet.

Ability to influence reaction speed when driving vehicles or other mechanisms

Not installed.

Use during pregnancy or breastfeeding

Contraindicated during pregnancy or breastfeeding.

Method of administration and doses

Women (adults)

Dissolve the contents of one sachet in 1 glass of water.

Take 1 sachet orally 3 times a day for 48 hours.

The prepared solution must be used immediately.

Men and children

Not recommended.

Children

Not recommended.

Overdose

An overdose of the drug is unlikely.

Symptoms: In case of excessive use of sodium citrate, gastrointestinal discomfort and diarrhea may occur. Overdose of sodium salts may lead to hypernatremia and hyperosmolarity. Excessive use of bicarbonates may lead to hypokalemia and metabolic alkalosis, especially in patients with impaired renal function.

Treatment: symptomatic, including appropriate correction of water and electrolyte balance.

Adverse reactions

Immune system disorders: hypersensitivity reactions, including skin rashes.

Gastrointestinal: abdominal pain.

On the part of the kidneys and urinary system: moderate increase in diuresis.

Expiration date

3 years.

Storage conditions

Store at a temperature not exceeding 25 °C in the original packaging.

Keep out of reach of children.

Packaging

5.6 g of granules per sachet. 6 sachets per carton.

Vacation category

Without a prescription.

Producer

Kusum Healthcare Pvt Ltd.

Location of the manufacturer and its business address

Plot No. M-3, Indore Special Economic Zone, Phase-II, Pithampur, Dist. Dhar, Madhya Pradesh, Pin 454774, India