Urocit-K® – Healthcare Professionals - GrupoFarma Ecuador


Potassium citrate.

Bottle, 100 Extended Release Tablets, 10 Millimeters.

Treatment of renal lithiasis.
Recurrence prophylaxis in the formation of kidney stones.

2 tablets per day up to 100 mEq.

Adrenal insufficiency, renal insufficiency, respiratory or metabolic alkalosis, intestinal obstruction, active gastric ulcer.

Adverse effects
Mild gastrointestinal disorders may occur, such as: dyspepsia, nausea, vomiting, diarrhea, which can be reduced by co-administration with food.

Interaction with other Medications
Drug interactions:
Concomitant administration of UROCIT® K and potassium-sparing diuretics should be avoided. MEDICINES THAT DELAY INTESTINAL TRANSIT TIME (such as anticholinergics) may increase the gastrointestinal irritation produced by potassium salts.

Laboratory tests:
Regular potassium determinations are recommended. Careful attention should be paid to the acid-base balance, levels of other serum electrolytes, the electrocardiogram, and the clinical status of the patient.

Do not administer during pregnancy or when its existence is suspected, or during lactation. The active ingredient is released from the wax matrix to exert its effect. The matrix is ​​an inert carrier and can be excreted unchanged in the feces.


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The information provided on this website was prepared by GrupoFarma S.A. and directed exclusively to medical personnel and health professionals. It may NOT be considered general use for people, nor as medical advice, recommendations or medical advice of any kind. We suggest not to self-medicate and consult your doctor beforehand about any concerns related to the information on the products or drugs mentioned here. Laboratories Farma S.A. will not be responsible for the misuse that third parties may give to the information obtained here.