Logo

OpiCalc

FavoritesSpecialtiesDrugsGuidelinesMost Used

Quick Access

Favorites
Most Used

All Specialties

OpiCalc Logo
Clinical CalculatorsDrugsGuidelines
SpecsDrugsGuides
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
OpiCalc Logo

OpiCalc

Easy, fast, and private medical tools for clinicians. Always free.

No Login Required
Ready for the Bedside

Resources

About UsEditorial PolicyMedical DisclaimerPrivacy PolicyTerms of UseCookie Policy

Support

Contact Us

Clinical Notice:OpiCalc is not a substitute for professional clinical judgment. Always verify dosages and guidelines.

OpiCalc © 2018-2026

•

All Rights Reserved

Registry Hub
Electrolyte Supplement/Discontinued

POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5% IN PLASTIC CONTAINER

POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5% IN PLASTIC CONTAINER

Clinical safety rating

caution

Comprehensive clinical and safety monograph for POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5% IN PLASTIC CONTAINER (POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5% IN PLASTIC CONTAINER).


Mechanism of Action

Potassium is the principal intracellular cation and is essential for maintaining cellular membrane potential, nerve impulse transmission, and muscle contraction. Dextrose provides calories and may prevent ketosis.

What the body does with it

MetabolismPotassium is not metabolized; it is excreted primarily by the kidneys. Dextrose undergoes glycolysis and oxidation to carbon dioxide and water.
ExcretionRenal: >90% of potassium intake is excreted by the kidneys, primarily via distal tubular secretion; fecal: <10%; minor sweat losses. In this formulation (KCl 0.22% in D5W), the potassium content is 2 mEq per 100 mL (approximately 20 mEq/L).
Half-lifeThe elimination half-life of potassium is not applicable in the traditional sense because potassium is an endogenous ion under tight homeostatic control. After intravenous infusion of a potassium load, the plasma concentration declines with a distribution phase of about 1-2 hours, followed by a slower elimination phase reflecting cellular uptake and renal excretion, with a terminal half-life of approximately 6-8 hours in patients with normal renal function.
Protein bindingNegligible (<5%). Potassium is not significantly bound to plasma proteins; it exists as free ion in serum.
Volume of DistributionApproximately 0.5-0.6 L/kg (total body water); reflects distribution throughout extracellular and intracellular spaces. Potassium is predominantly intracellular (98% of total body potassium is in cells); Vd for administered potassium is large due to cellular uptake.
BioavailabilityIntravenous: 100% (complete bioavailability). Oral: about 90% absorbed; however, this formulation is for IV administration only.
Onset of ActionIntravenous: Correction of hypokalemia begins within minutes after starting infusion; clinical effect (e.g., improvement in muscle weakness, ECG changes) seen within 30-60 minutes at appropriate infusion rates (usual rate: 10-20 mEq/h; max 40 mEq/h with cardiac monitoring).
Duration of ActionIntravenous: Effect persists for the duration of infusion and several hours thereafter; potassium levels gradually return to baseline over 6-12 hours post-infusion, depending on ongoing losses and cellular uptake. Continuous infusion required for sustained correction of severe depletion.
Molecular Weight74.55

Classification & Brands

Dosing & administration

Intravenous; typical adult dose is 10-20 mEq/hour, not exceeding 40 mEq/hour or 150 mEq/day, with continuous cardiac monitoring and serum potassium monitoring.

Dosage formINJECTABLE
Renal impairmentGFR > 50 mL/min: no adjustment; GFR 10-50 mL/min: reduce total daily dose by 25-50%; GFR < 10 mL/min: reduce dose by 50-75% and monitor potassium closely. Avoid if anuria.
Liver impairmentNo specific adjustment based on Child-Pugh score; however, monitor potassium levels and renal function closely due to potential hepatorenal syndrome.
Pediatric useIntravenous; 0.2-0.5 mEq/kg/hour, not exceeding 1 mEq/kg/hour or 40 mEq/m²/hour; adjust based on serum potassium and clinical status.
Geriatric useCautious dosing: initial dose at lower end of adult range (10 mEq/hour) with close monitoring of renal function and serum potassium due to decreased renal reserve and higher risk of hyperkalemia.

Use during pregnancy

1st trimesterPotassium chloride and dextrose are generally considered safe in pregnancy when used as electrolyte replacement. No teratogenic effects reported at therapeutic doses.
2nd trimesterSafe for use in pregnancy. May be used to correct hypokalemia. Dextrose provides calories and may be beneficial in hyperemesis.
3rd trimesterSafe for use in pregnancy. Monitor maternal electrolytes and fetal well-being if used for prolonged periods or in high doses.

Clinical note

Comprehensive clinical and safety monograph for POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5% IN PLASTIC CONTAINER (POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5% IN PLASTIC CONTAINER).

Placental transferPotassium crosses the placenta via active transport. Dextrose crosses easily. Both are physiologic substances.
BreastfeedingPotassium chloride and dextrose are normal constituents of breast milk. Use during breastfeeding is considered safe. No adverse effects in infants reported from maternal infusion.
Lactation RatingL1 (safest)
Teratogenic RiskPotassium chloride and dextrose are not known to be teratogenic. No fetal risks have been identified in any trimester. Dextrose is a physiological nutrient. Overdose or rapid infusion may cause maternal electrolyte imbalance potentially affecting fetus.
Fetal MonitoringMonitor serum potassium and glucose levels, fluid balance, and renal function. Monitor fetal heart rate during infusion if indicated.
Fertility EffectsNo known adverse effects on fertility.

Warnings & precautions

■ FDA Black Box Warning

Potassium chloride injection concentrate must be diluted before use to avoid fatal hyperkalemia.

Side Effect Profile

Serious Effects

Absolute Contraindications

HyperkalemiaSevere renal impairment with oliguria or anuriaAddison's diseaseHyperchloremiaMetabolic alkalosis

Clinical Precautions

PrecautionsHyperkalemia risk; monitor serum potassium levels, Cardiotoxicity; ECG monitoring recommended, Risk of extravasation; do not administer intramuscularly, Use with caution in renal impairment, adrenal insufficiency, or conditions predisposing to hyperkalemia, Do not administer if solution is discolored or contains particulate matter
Food/DietaryAvoid excessive intake of potassium-rich foods (e.g., bananas, oranges, tomatoes, potatoes, spinach, salt substitutes) while receiving this IV solution to prevent hyperkalemia.

Clinical Tips & Counseling

Clinical PearlsThis solution provides 22 mEq/L of potassium chloride and 5% dextrose. Use with caution in patients with renal impairment, cardiac disease, or hyperkalemia. Monitor serum potassium levels closely; rate of infusion should not exceed 10 mEq/hour typically. Avoid in patients with oliguria or anuria. Do not administer undiluted; container is for intravenous use only.
Patient AdviceThis medication is given through a vein to provide potassium and sugar. · Tell your healthcare provider if you have kidney problems, heart disease, or are taking any other medications. · Report any symptoms of high potassium such as muscle weakness, irregular heartbeat, or tingling sensations. · You may experience pain or irritation at the IV site; inform your nurse if this occurs. · Do not stop or change the infusion rate on your own.

POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5% IN PLASTIC CONTAINER Interactions

Loading safety data…

This overview is compiled from peer-reviewed clinical sources and FDA labeling. It's here to support — not replace — clinical judgment. Always verify dosing against your institution's current protocols before prescribing.

On this page

Mechanism of ActionDosing & administrationUse during pregnancyWarnings & precautionsDrug interactions

Compare with

CALCIUM CHLORIDE 10%CALCIUM CHLORIDE 10% IN PLASTIC CONTAINERCALCIUM GLUCEPTATECALCIUM GLUCONATEHEMICLOR

External sources

DailyMed (NIH) PubMed OpenFDA