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Potassium Chloride for Oral Solution
Overview
What is Potassium Chloride for Oral Solution?
Potassium Chloride is a white crystalline or colorless solid. It is soluble in water and slightly soluble in alcohol. Chemically, Potassium Chloride is K-Cl with a molecular mass of 74.55.
Each pouch of light pink to orange powder contains 1.5 g of potassium chloride, USP, which is equivalent to potassium 20 mEq and chloride 20 mEq and the following inactive ingredients: citric acid anhydrous, colloidal silicon dioxide, FD&C Yellow #6, natural and artificial orange flavor, and sucralose.
What does Potassium Chloride for Oral Solution look like?
What are the available doses of Potassium Chloride for Oral Solution?
Each pouch contains 1.5 g of potassium chloride supplying 20 mEq of potassium and 20 mEq of chloride.
What should I talk to my health care provider before I take Potassium Chloride for Oral Solution?
Cirrhosis: Initiate therapy at the low end of the dosing range ()
Renal Impairment: Initiate therapy at the low end of the dosing range ()
How should I use Potassium Chloride for Oral Solution?
Potassium Chloride 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 is insufficient.
If serum potassium concentration is <2.5 mEq/L, use intravenous potassium instead of oral supplementation.
What interacts with Potassium Chloride for Oral Solution?
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What are the warnings of Potassium Chloride for Oral Solution?
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What are the precautions of Potassium Chloride for Oral Solution?
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What are the side effects of Potassium Chloride for Oral Solution?
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What should I look out for while using Potassium Chloride for Oral Solution?
Potassium chloride is contraindicated in patients on potassium sparing diuretics.
What might happen if I take too much Potassium Chloride for Oral Solution?
How should I store and handle Potassium Chloride for Oral Solution?
KADCYLA (ado-trastuzumab emtansine) is supplied as:Potassium Chloride for Oral Solution, is a light pink to orange powder available in one strength as follows:20 mEqNDC# 69543-379-01 pouch. Each pouch contains 1.5 g of potassium chloride providing potassium 20 mEq and chloride 20 mEqNDC# 69543-379-30 carton of 30 pouchesNDC# 69543-379-10 carton of 100 pouchesPotassium Chloride for Oral Solution, is a light pink to orange powder available in one strength as follows:20 mEqNDC# 69543-379-01 pouch. Each pouch contains 1.5 g of potassium chloride providing potassium 20 mEq and chloride 20 mEqNDC# 69543-379-30 carton of 30 pouchesNDC# 69543-379-10 carton of 100 pouches
Clinical Information
Chemical Structure
No Image foundClinical Pharmacology
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.
Non-Clinical Toxicology
Potassium chloride is contraindicated in patients on potassium sparing diuretics.The most common adverse reactions to oral potassium salts are nausea, vomiting, flatulence, abdominal pain/discomfort, and diarrhea.
Reference
This information is obtained from the National Institute of Health's Standard Packaging Label drug database.
"https://dailymed.nlm.nih.gov/dailymed/"
While we update our database periodically, we cannot guarantee it is always updated to the latest version.
Review
Professional
Clonazepam Description Each single-scored tablet, for oral administration, contains 0.5 mg, 1 mg, or 2 mg Clonazepam, USP, a benzodiazepine. Each tablet also contains corn starch, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and povidone. Clonazepam tablets USP 0.5 mg contain Yellow D&C No. 10 Aluminum Lake. Clonazepam tablets USP 1 mg contain Yellow D&C No. 10 Aluminum Lake, as well as FD&C Blue No. 1 Aluminum Lake. Chemically, Clonazepam, USP is 5-(o-chlorophenyl)-1,3-dihydro-7-nitro-2H-1,4-benzodiazepin-2-one. It is a light yellow crystalline powder. It has the following structural formula: C15H10ClN3O3 M.W. 315.72Tips
Tips
Interactions
Interactions
A total of 440 drugs (1549 brand and generic names) are known to interact with Imbruvica (ibrutinib). 228 major drug interactions (854 brand and generic names) 210 moderate drug interactions (691 brand and generic names) 2 minor drug interactions (4 brand and generic names) Show all medications in the database that may interact with Imbruvica (ibrutinib).