KCL in NS
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KCL in NS
KCL in NS Side Effects Center
Medical Editor: John P. Cunha, DO, FACOEP
KCL in NS (potassium chloride in sodium chloride injection) is a fluid and electrolyte replenisher used as a source of water and electrolytes. Common side effects of KCL in NS include fever, infection, redness, pain, or swelling at the injection site.
Dosage of KCL in NS is dependent upon the age, weight and clinical condition of the patient as well as laboratory determinations. KCL in NS may interact with other drugs. Tell your doctor all medications and supplements you use. During pregnancy, KCL in NS should be used only if prescribed. It is unknown if this drug passes into breast milk. Consult your doctor before breastfeeding.
Our KCL in NS (potassium chloride in sodium chloride injection) Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication.
This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
What is Prescribing information?
The FDA package insert formatted in easy-to-find categories for health professionals and clinicians.
KCL in NS FDA Prescribing Information: Side Effects
Reactions which may occur because of the solution or the technique of administration include febrile response, infection at the site of injection, venous thrombosis or phlebitis extending from the site of injection, extravasation and hypervolemia.
If an adverse reaction does occur, discontinue the infusion, evaluate the patient, institute appropriate therapeutic countermeasures and save the remainder of the fluid for examination if deemed necessary.
Read the entire FDA prescribing information for KCL in NS (Potassium Chloride in Sodium Chloride Injection)
Additional KCL in NS Information
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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