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סלו-ק SLOW - K (POTASSIUM CHLORIDE)

תרופה במרשם תרופה בסל נרקוטיקה ציטוטוקסיקה

צורת מתן:

פומי : PER OS

צורת מינון:

אין פרטים : TABLETS, SUGAR COATED, PROLONGED RELEASE

Pharmacological properties : תכונות פרמקולוגיות

Pharmacodynamic Properties

5.1 Pharmacodynamic properties

Pharmacotherapeutic group: Potassium supplement, ATC code: A12BA01 

SLO API JUN16 CL V3                               REF Ireland_PI_effective_Feb-2016 Potassium, as the most abundant intracellular cation, plays an essential role in several important physiological functions, including transmission of nerve impulses, contraction of cardiac, skeletal, and smooth-muscle tissues, and maintenance of normal renal function. It also aids in the regulation of osmotic pressure and the acid- based balance. Concentrations of K+ range in intracellular fluid from 130 to 150 up to 160 mmol/L and in plasma from 3.5 to 5 mmol/L. Although there is no uniform correlation between plasma concentrations of potassium and total body stores, clinical signs of K+ deficiency are usually observed whenever the plasma potassium concentration falls below 3.5 mmol/L (hypokalemia). These signs include: impaired neuromuscular function, which may vary from minimal weakness to frank paralysis; intestinal dilatation and ileus; and, more frequently, abnormalities myocardial function with disturbed ECG patterns characterized by a prolonged PR interval, an exaggerated U wave, a broad and flat T wave, and a depressed ST segment.


Hypokalemia can be prevented and/or corrected by giving supplementary potassium.
Apart from increasing dietary intake of potassium-rich foods, which may not always be practicable, a suitable alternative is to administer Slow-K. In view of the frequency with which deficits of K+ and CL- coexist, potassium chloride is the preferred salt for most of the clinical conditions associated with hypokalemia.

Pharmacokinetic Properties

5.2 Pharmacokinetic properties


Absorption

Following a single dose of Slow K, potassium chloride is released over a period of approximately 4 hours. Renal excretion of potassium chloride following ingestion of Slow K occurs 30-60 minutes later than when the same dose is given in the form of a solution.


Elimination
In the presence of a normal potassium balance 90% of the potassium supplied by Slow K is excreted renally within 8 hours and more than 98% by 24 hours.


Special population
Elderly Patients
No pharmacokinetics studies of potassium chloride are reported in elderly population.
However, these patients are more likely to develop hyperkalemia due to physiological changes, and reduced renal function.
Pediatrics
No pharmacokinetics studies of potassium chloride are reported in the pediatric population.
Hepatic impairment
No pharmacokinetics studies of potassium chloride are reported in patients with hepatic impairment.
Renal impairment
SLO API JUN16 CL V3                                REF Ireland_PI_effective_Feb-2016 Potassium is almost completely excreted via urine and its excretion rate highly correlates with the glomerular filtration rate. Considering the possibility of hyperkalemia in these patients and severity of outcome, Slow-K is contraindicated in patients with severe renal impairment. If used in patients with mild to moderate renal impairment, extreme caution along with frequent serum potassium monitoring is recommended.


שימוש לפי פנקס קופ''ח כללית 1994 Potassium supplement
תאריך הכללה מקורי בסל 01/01/1995
הגבלות תרופה שאושרה לשימוש כללי בקופ'ח

בעל רישום

NOVARTIS ISRAEL LTD

רישום

115 88 22133 01

מחיר

0 ₪

מידע נוסף

עלון מידע לרופא

28.07.16 - עלון לרופא

עלון מידע לצרכן

28.07.16 - עלון לצרכן אנגלית 28.07.16 - עלון לצרכן עברית 28.07.16 - עלון לצרכן ערבית

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