Adult: Dose and rate of administration are dependent upon the patient’s ECG and serum K levels. Recommended administration rates: Peripheral or central line infusion: ≤10 mEq/hour. Central line infusion: >10 mEq/hour, guided by continuous ECG monitoring and frequent serum K determination. Administer doses as a dilute solution via slow IV infusion. Dosage and infusion rate recommendations may vary in the country of use (refer to specific local treatment guidelines).
Adult: Dosage is individualised and adjusted based on patient’s need and serum K levels. As extended-release tab/cap: Prophylaxis: Usual dose: 20 mEq daily. Treatment: Usual dose range: 40-100 mEq daily in divided doses. Max: 20 mEq/dose. As powder for oral solution: Prophylaxis: Usual dose: 20 mEq daily. Treatment: Usual dose range: 40-100 mEq daily in 2-5 divided doses. Max: 40 mEq/dose; 200 mEq daily. Child: Dosage is individualised and adjusted based on patient’s need and serum K levels. As powder for oral solution: Prophylaxis: Usual dose: 1 mEq/kg daily. Max: 3 mEq/kg daily. Treatment: Initially, 2-4 mEq/kg daily in divided doses. Max: 1 mEq/kg/dose or 40 mEq/dose (whichever is lower); 100 mEq daily.
Cirrhosis: As powder for oral solution/extended-release tab: Initiate dose at the lower end of the dosing range.
Should be taken with food.
Powder for oral solution: Dissolve the contents of 1 packet in at least 120 mL of cold water or other beverage before administration. IV infusion concentrate: Dilute with at least 50 times its volume of 0.9% NaCl infusion or other suitable diluent and mixed thoroughly prior to administration. Do not administer undiluted or via IV push or rapid IV infusion.
Hyperkalaemia, hyperchloraemia, predisposing conditions for hyperkalaemia (e.g. acute dehydration, systemic acidosis, extensive burns or tissue injury); adrenal insufficiency (e.g. Addison’s disease), heat cramps, renal failure, renal impairment with oliguria, anuria or azotaemia; plasma-K concentration >5 mEq/L. Tab/cap: Structural, pathological (e.g. diabetic gastroparesis), and/or pharmacologic (e.g. use of anticholinergics) cause for arrest or delay in gastrointestinal passage. Severe renal impairment. Concomitant use with K-sparing diuretics.
Patient with acid-base alterations or correction; CV disease (e.g. heart failure, cardiac arrhythmias, atrioventricular block), cirrhosis. Avoid extravasation (IV). Hepatic and mild to moderate renal impairment. Children and elderly. Pregnancy and lactation.
Significant: IV infusion: Hypersensitivity/infusion reactions (e.g. anaphylaxis, chills), hyponatraemia. Oral: Gastrointestinal irritation (oral solution); ulcerative and/or stenotic lesions of the gastrointestinal tract (tab/cap). Gastrointestinal disorders: Nausea, vomiting, flatulence, abdominal pain or discomfort, diarrhoea; gastrointestinal haemorrhage, ulceration, perforation (tab/cap). Metabolism and nutrition disorders: Hypervolaemia. Injury, poisoning and procedural complications: Inj site reactions (e.g. pain, phlebitis, venous thrombosis). Potentially Fatal: Hyperkalaemia.
Closely monitor serum K concentrations and other electrolyte levels (e.g. serum Ca, chloride, Mg, phosphate, Na), acid-base balance, renal function, IV infusion rate, cardiac, clinical and fluid status prior to initiation and regularly during treatment. Perform ECG monitoring regularly.
Symptoms: Paraesthesia of the extremities, listlessness, mental confusion, cold skin, grey pallor, weakness or heaviness of the legs, flaccid paralysis, peripheral vascular collapse, fall in blood pressure, cardiac arrhythmias, heart block, and extremely high plasma K concentration (8-11 mEq/L) causing cardiac depression, arrhythmias or arrest. Management: Discontinue K chloride, other agents and foods with K or which increases serum K levels. Correct serum K levels and acid-base balance. May administer Ca gluconate (except in patients on digitalis) to reduce cardiac effects. May give IV infusion of 300-500 mL/hour 10% glucose solutions containing up to 10 units of insulin for each 20 g of glucose to reduce serum K levels. May administer IV Na bicarbonate to correct acidosis, if present. Continuously monitor ECG for arrhythmias and electrolyte changes especially serum K levels.
May increase the risk of hyperkalaemia with ACE inhibitors, angiotensin II receptor antagonists, ciclosporin, aliskiren. May enhance the antiarrhythmic effects of quinidine. May cause K retention with NSAIDs. May enhance the ulcerogenic effect of solid oral dosage forms of K chloride with anticholinergic agents. May cause further decrease in plasma K concentration with glucose infusion (IV). Potentially Fatal: Increased risk of severe hyperkalaemia with K-sparing diuretics (e.g. spironolactone, amiloride, triamterene).
May increase the risk of hyperkalaemia with K-rich foods.
Description: Mechanism of Action: Potassium chloride is a major cation of intracellular fluid. It is essential in physiological processes, including conduction of nerve impulses in heart, brain, and skeletal muscle; contraction of cardiac, skeletal and smooth muscles; maintenance of normal renal function, carbohydrate metabolism, acid-base balance, and gastric secretion. Pharmacokinetics: Absorption: Well and readily absorbed from gastrointestinal tract. Distribution: Distributed into cells via active transport from extracellular fluid. Excretion: Mainly via urine; faeces and sweat (small amounts).
Store between 20-25°C. Protect from light and moisture.
B05XA01 - potassium chloride ; Belongs to the class of electrolyte solutions used in I.V. solutions. A12BA01 - potassium chloride ; Belongs to the class of potassium-containing preparations. Used as dietary supplements.
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