Product Elements:
Potassium chloride potassium chloride potassium chloride potassium cation chloride ion anhydrous citric acid fd&c yellow no. 6 glycerin methylparaben propylene glycol propylparaben trisodium citrate dihydrate sucralose water orange potassium chloride potassium chloride potassium chloride potassium cation chloride ion anhydrous citric acid fd&c yellow no. 6 glycerin methylparaben propylene glycol propylparaben trisodium citrate dihydrate sucralose water orange
Drug Interactions:
7 drug interactions potassium sparing diuretics: avoid concomitant use. ( 7.1 ) angiotensin converting enzyme inhibitors: monitor for hyperkalemia. ( 7.2 ) angiotensin receptor blockers: monitor for hyperkalemia. ( 7.3 ) 7.1 potassium-sparing diuretics use with potassium-sparing diuretic can produce severe hyperkalemia. avoid concomitant use. 7.2 angiotensin-converting enzyme inhibitors use with angiotensin converting enzyme (ace) inhibitors produces potassium retention by inhibiting aldosterone production. potassium supplements should be given to patients receiving ace inhibitors only with close monitoring. 7.3 angiotensin receptor blockers use with angiotensin receptor blockers (arbs) produces potassium retention by inhibiting aldosterone production. potassium supplements should be given to patients receiving arbs only with close monitoring.
Indications and Usage:
1 indications and usage potassium chloride oral solution is indicated for the treatment and prophylaxis of hypokalemia in patients for whom dietary management with potassium-rich foods or diuretic dose reduction are insufficient. potassium chloride oral solution is indicated for the treatment and prophylaxis of hypokalemia with or without metabolic alkalosis, in patients for whom dietary management with potassium-rich foods or diuretic dose reduction are insufficient. ( 1 )
Warnings and Cautions:
5 warnings and precautions gastrointestinal irritation : dilute before use, take with meals. ( 5.1 ) 5.1 gastrointestinal irritation may cause gastrointestinal irritation if administered undiluted. increased dilution of the solution and taking with meals may reduce gastrointestinal irritation [see dosage and administration ( 2.1 )] .
Dosage and Administration:
2 dosage and administration dilute prior to administration. ( 2.1 , 5.1 ) monitor serum potassium and adjust dosage accordingly. ( 2.2 , 2.3 ) treatment of hypokalemia: adults: initial doses range from 40 to 100 meq/day in 2 to 5 divided doses: limit doses to 40 meq per dose. total daily dose should not exceed 200 meq. ( 2.2 ) pediatric patients aged birth to 16 years old: 2 to 4 meq/kg/day in divided doses; not to exceed 1 meq/kg as a single dose or 20 meq whichever is lower; if deficits are severe or ongoing losses are great, consider intravenous therapy. total daily dose should not exceed 100 meq. ( 2.3 ) maintenance or prophylaxis of hypokalemia: adults: typical dose is 20 meq per day. ( 2.2 ) pediatric patients aged birth to 16 years old: typical dose is 1 meq/kg/day. do not to exceed 3 meq/kg/day. ( 2.3 ) 2.1 administration and monitoring monitoring monitor serum potassium and adjust dosages accordingly. for treatment of hypokalemia, monitor potassium levels daily or more often d
Read more...epending on the severity of hypokalemia until they return to normal. monitor potassium levels monthly-to-biannually for maintenance or prophylaxis. the treatment of potassium depletion, particularly in the presence of cardiac disease, renal disease, or acidosis requires careful attention to acid-base balance, volume status, electrolytes, including magnesium, sodium, chloride, phosphate, and calcium, electrocardiograms and the clinical status of the patient. correct volume status, acid-base balance and electrolyte deficits as appropriate. administration dilute the potassium chloride solution with at least 4 ounces of cold water [see warnings and precautions ( 5.1 )] . take with meals or immediately after eating. if serum potassium concentration is less than 2.5 meq/l, use intravenous potassium instead of oral supplementation. 2.2 adult dosing treatment of hypokalemia daily dose range from 40 to 100 meq. give in 2 to 5 divided doses: limit doses to 40 meq per dose. the total daily dose should not exceed 200 meq in a 24 hour period. maintenance or prophylaxis typical dose is 20 meq per day. individualize dose based upon serum potassium levels. studies support the use of potassium replacement in digitalis toxicity. when alkalosis is present, normokalemia and hyperkalemia may obscure a total potassium deficit. the advisability of use of potassium replacement in the setting of hyperkalemia is uncertain. 2.3 pediatric dosing treatment of hypokalemia pediatric patients aged birth to 16 years old: the initial dose is 2 to 4 meq/kg/day in divided doses; do not exceed as a single dose 1 meq/kg or 40 meq, whichever is lower; maximum daily doses should not exceed 100 meq. if deficits are severe or ongoing losses are great, consider intravenous therapy. maintenance or prophylaxis pediatric patients aged birth to 16 years old: typical dose is 1 meq/kg/day. do not exceed 3 meq/kg/day.
Dosage Forms and Strength:
3 dosage forms and strengths oral solution 10%: 1.3 meq potassium per ml. oral solution 20%: 2.6 meq potassium per ml. oral solution: 10%; 1.3 meq potassium per ml ( 3 ) oral solution: 20%; 2.6 meq potassium per ml ( 3 )
Contraindications:
4 contraindications potassium chloride is contraindicated in patients on potassium sparing diuretics. concomitant use with potassium sparing diuretics. ( 4 )
Adverse Reactions:
6 adverse reactions the most common adverse reactions to oral potassium salts are nausea, vomiting, flatulence, abdominal pain/discomfort, and diarrhea. most common adverse reactions are nausea, vomiting, flatulence, abdominal pain/discomfort, and diarrhea. ( 6 ) to report suspected adverse reactions, contact apotex corp. at 1-800-706-5575 or fda at 1-800-fda-1088 or www.fda.gov/medwatch.
Drug Interactions:
7 drug interactions potassium sparing diuretics: avoid concomitant use. ( 7.1 ) angiotensin converting enzyme inhibitors: monitor for hyperkalemia. ( 7.2 ) angiotensin receptor blockers: monitor for hyperkalemia. ( 7.3 ) 7.1 potassium-sparing diuretics use with potassium-sparing diuretic can produce severe hyperkalemia. avoid concomitant use. 7.2 angiotensin-converting enzyme inhibitors use with angiotensin converting enzyme (ace) inhibitors produces potassium retention by inhibiting aldosterone production. potassium supplements should be given to patients receiving ace inhibitors only with close monitoring. 7.3 angiotensin receptor blockers use with angiotensin receptor blockers (arbs) produces potassium retention by inhibiting aldosterone production. potassium supplements should be given to patients receiving arbs only with close monitoring.
Use in Specific Population:
8 use in specific populations 8.1 pregnancy pregnancy category c animal reproduction studies have not been conducted with potassium chloride. it is unlikely that potassium supplementation that does not lead to hyperkalemia would have an adverse effect on the fetus or would affect reproductive capacity. 8.2 nursing mothers the normal potassium ion content of human milk is about 13 meq per liter. since oral potassium becomes part of the body potassium pool, so long as body potassium is not excessive, the contribution of potassium chloride supplementation should have little or no effect on the level in human milk. 8.3 pediatric use the safety and effectiveness of potassium chloride have been demonstrated in children with diarrhea and malnutrition from birth to18 years. 8.4 geriatric use clinical studies of potassium chloride did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. other reported clinical experienc
Read more...e has not identified differences in responses between the elderly and younger patients. in general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy. this drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function. because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function.
Use in Pregnancy:
8.1 pregnancy pregnancy category c animal reproduction studies have not been conducted with potassium chloride. it is unlikely that potassium supplementation that does not lead to hyperkalemia would have an adverse effect on the fetus or would affect reproductive capacity.
Pediatric Use:
8.3 pediatric use the safety and effectiveness of potassium chloride have been demonstrated in children with diarrhea and malnutrition from birth to18 years.
Geriatric Use:
8.4 geriatric use clinical studies of potassium chloride did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. other reported clinical experience has not identified differences in responses between the elderly and younger patients. in general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy. this drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function. because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function.
Overdosage:
10 overdosage 10.1 symptoms the administration of oral potassium salts to persons with normal excretory mechanisms for potassium rarely causes serious hyperkalemia. however, if excretory mechanisms are impaired or if potassium is administered too rapidly potentially fatal hyperkalemia can result. hyperkalemia is usually asymptomatic and may be manifested only by an increased serum potassium concentration (6.5 to 8.0 meq/l) and characteristic electrocardiographic changes (peaking of t-waves, loss of p-waves, depression of s-t segment, and prolongation of the qt-interval). late manifestations include muscle paralysis and cardiovascular collapse from cardiac arrest (9 to12 meq/l). 10.2 treatment treatment measures for hyperkalemia include the following: monitor closely for arrhythmias and electrolyte changes. eliminate foods and medications containing potassium and of any agents with potassium-sparing properties such as potassium-sparing diuretics, arbs, ace inhibitors, nsaids, certain nutritional supplements and many others. administer intravenous calcium gluconate if the patient is at no risk or low risk of developing digitalis toxicity. administer intravenously 300 to 500 ml/hr of 10% dextrose solution containing 10 to 20 units of crystalline insulin per 1000 ml. correct acidosis, if present, with intravenous sodium bicarbonate. use exchange resins, hemodialysis, or peritoneal dialysis. in patients who have been stabilized on digitalis, too rapid a lowering of the serum potassium concentration can produce digitalis toxicity.
Description:
11 description potassium chloride, usp is a colorless, elongated, prismatic, or cubical crystals, or white, granular powder. it is soluble in water and slightly soluble in alcohol. chemically, potassium chloride is k-cl with a molecular mass of 74.55 g/mol. oral solution 10%: each 15 ml of solution contains 1.5 g of potassium chloride, usp and the following inactive ingredients: citric acid anhydrous, fd&c yellow #6, glycerin, methylparaben, natural orange flavor, propylene glycol, propylparaben, purified water, sodium citrate dihydrate, sucralose. oral solution 20%: each 15 ml of solution contains 3.0 g of potassium chloride, usp and the following inactive ingredients: citric acid anhydrous, fd&c yellow #6, glycerin, methylparaben, natural orange flavor, propylene glycol, propylparaben, purified water, sodium citrate dihydrate, sucralose. natural orange flavor includes fruit extract and natural flavor.
Clinical Pharmacology:
12 clinical pharmacology 12.1 mechanism of action the potassium ion (k + ) is the principal intracellular cation of most body tissues. potassium ions participate in a number of essential physiological processes including the maintenance of intracellular tonicity; the transmission of nerve impulses; the contraction of cardiac, skeletal, and smooth muscle; and the maintenance of normal renal function. the intracellular concentration of potassium is approximately 150 to 160 meq per liter. the normal adult plasma concentration is 3.5 to 5 meq per liter. an active ion transport system maintains this gradient across the plasma membrane. potassium is a normal dietary constituent, and under steady-state conditions the amount of potassium absorbed from the gastrointestinal tract is equal to the amount excreted in the urine. the usual dietary intake of potassium is 50 to 100 meq per day. 12.3 pharmacokinetics based on published literature, the rate of absorption and urinary excretion of potassiu
Read more...m from kcl oral solution were higher during the first few hours after dosing relative to modified release kcl products. the bioavailability of potassium, as measured by the cumulative urinary excretion of k + over a 24 hour post dose period, is similar for kcl solution and modified release products.
Mechanism of Action:
12.1 mechanism of action the potassium ion (k + ) is the principal intracellular cation of most body tissues. potassium ions participate in a number of essential physiological processes including the maintenance of intracellular tonicity; the transmission of nerve impulses; the contraction of cardiac, skeletal, and smooth muscle; and the maintenance of normal renal function. the intracellular concentration of potassium is approximately 150 to 160 meq per liter. the normal adult plasma concentration is 3.5 to 5 meq per liter. an active ion transport system maintains this gradient across the plasma membrane. potassium is a normal dietary constituent, and under steady-state conditions the amount of potassium absorbed from the gastrointestinal tract is equal to the amount excreted in the urine. the usual dietary intake of potassium is 50 to 100 meq per day.
Pharmacokinetics:
12.3 pharmacokinetics based on published literature, the rate of absorption and urinary excretion of potassium from kcl oral solution were higher during the first few hours after dosing relative to modified release kcl products. the bioavailability of potassium, as measured by the cumulative urinary excretion of k + over a 24 hour post dose period, is similar for kcl solution and modified release products.
How Supplied:
16 how supplied/storage and handling potassium chloride oral solution, usp is an orange solution available in two strengths as follows: 10%: 20 meq/15 ml oral solution ndc# 48433-217-15 unit dose cup of 15 ml ndc# 48433-217-40 box of 40 unit dose cups, each with 15 ml 20%: 40 meq/15 ml oral solution ndc# 48433-218-15 unit dose cup of 15 ml ndc# 48433-218-40 box of 40 unit dose cups, each with 15 ml for institutional use only this package is not child resistant storage store at 20°c to 25°c (68°f to 77°f) [see usp controlled room temperature]. protect from light. potassium chloride oral solution, usp, 10% and 20% packaged by: safecor health, llc 4060 business park drive columbus, oh 43204 manufactured by: apotex inc. toronto, ontario canada m9l 1t9 manufactured for: apotex corp. weston, florida usa 33326 rev: 03/2019 pn5644
Package Label Principal Display Panel:
Principal display panel - 10% box label safecor health ndc: 48433-217-40 potassium chloride oral solution usp 10% contains 40 (15ml) unit dose cups see package insert for complete drug information store at 20° to 25°c (68° to 77°f) see usp controlled room temperature keep this and all drugs out of reach of children rx only for institutional use only pkg by: safecor health, llc columbus, oh 43204. questions or comments: cal 1-800-447-1006 gtn: 00348433217405 sn: 192000028 exp: 201212 lot: sc050819 5682.a principal display panel - 10% box label
Principal display panel - 10% lid label delivers 15ml ndc 48433-217-15 potassium chloride oral solution usp 10% 20 meq/15 ml dilute before using pkg by: safecor health, llc columbus, oh 43204 pn5641.a principal display panel - 10% lid label
Principal display panel - 10% box label safecor health ndc: 48433-218-40 potassium chloride oral solution usp 20% contains 40 (15ml) unit dose cups see package insert for complete drug information store at 20° to 25°c (68° to 77°f) see usp controlled room temperature keep this and all drugs out of reach of children rx only for institutional use only pkg by: safecor health, llc columbus, oh 43204. questions or comments: cal 1-800-447-1006 gtn: 00348433218402 sn: 192000031 exp: 201213 lot: cs050819 5682.a principal display panel - 10% box label
Principal display panel - 20% lid label delivers 15ml ndc 48433-218-15 potassium chloride oral solution usp 20% 40 meq/15 ml dilute before using pkg by: safecor health, llc columbus, oh 43204 pn5641.a principal display panel - 20% lid label