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Slow-K

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Slow-K

SLOW-K
(potassium chloride) Tablet, Extended Release

Slow-K

DRUG DESCRIPTION

Slow-K, potassium chloride extended-release tablets USP, is a sugar-coated (not enteric-coated) tablet for oral administration, containing 600 mg of potassium chloride (equivalent to 8 mEq) in a wax matrix. This formulation is intended to provide an extended-release of potassium from the matrix to minimize the likelihood of producing high, localized concentrations of potassium within the gastrointestinal tract.

Slow-K (potassium chloride) is an electrolyte replenisher. Its chemical name is potassium chloride, and its structural formula is KCI. Potassium chloride USP is a white, granular powder or colorless crystals. It is odorless and has a saline taste. Its solutions are neutral to litmus. It is freely soluble in water and insoluble in alcohol.

Inactive Ingredients. Acacia, cetostearyl alcohol, gelatin, iron oxide, magnesium stearate, parabens, polyvinyl-pyrrolidone, sodium benzoate, starch, sucrose, talc, and titanium dioxide.

What are the precautions when taking potassium chloride (Slow-K)?

Before taking potassium, tell your doctor or pharmacist if you have any allergies. This product may contain inactive ingredients, which can cause allergic reactions or other problems. Talk to your pharmacist for more details.

Before using this medication, tell your doctor or pharmacist your medical history, especially of: heart problems, kidney problems, high levels of potassium in the blood.

Due to rare reports of stomach/intestinal ulcers and bleeding with sustained-release potassium products, taking a liquid form of potassium is preferred. Tell your doctor or pharmacist if you have throat/stomach/intestinal problems such as blockage, narrowing, or ulcers.

Before having surgery, tell your doctor or dentist about all the products you use (including prescription...

Read All Potential Precautions of Slow-K »

Last reviewed on RxList: 4/13/2009
This monograph has been modified to include the generic and brand name in many instances.

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Report Problems to the Food and Drug Administration

 

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.


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