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Electrolyte/Prescription

DEXTROSE 2.5% AND SODIUM CHLORIDE 0.33% IN PLASTIC CONTAINER

DEXTROSE 2.5% AND SODIUM CHLORIDE 0.33% IN PLASTIC CONTAINER

Clinical safety rating

safe

No significant drug interactions Can cause hypernatremia and fluid overload.


Mechanism of Action

Dextrose is a monosaccharide that provides caloric support and helps correct hypoglycemia. Sodium chloride is an electrolyte that maintains osmotic balance and fluid volume.

What the body does with it

MetabolismDextrose is metabolized via glycolysis and the citric acid cycle. Sodium chloride is not metabolized; it is excreted renally.
ExcretionDextrose is metabolized to CO2 and water via glycolysis and the Krebs cycle; negligible renal excretion (<5%). Sodium chloride is excreted renally with sodium and chloride ions freely filtered and variably reabsorbed (99% reabsorption under normal conditions, but excretion increases with excess intake).
Half-lifeNot applicable for dextrose as it is rapidly metabolized; plasma glucose half-life is approximately 1.7-2.0 hours after IV infusion but highly variable depending on metabolic demand and insulin activity. For sodium chloride, ions are continuously regulated by renal handling; no traditional half-life.
Protein bindingDextrose: negligible (<1%); not protein-bound. Sodium and chloride ions: negligible (<1%); are free ions in plasma.
Volume of DistributionDextrose: approximately 0.25-0.4 L/kg, reflecting distribution primarily into extracellular fluid and cells. Sodium chloride: sodium distributes mainly in extracellular fluid (Vd ~0.2 L/kg for sodium), chloride follows sodium distribution.
BioavailabilityIntravenous: 100% (complete bioavailability). No other relevant routes; oral dextrose is absorbed but formulation is for IV use only.
Onset of ActionIntravenous: Immediate (within seconds) for volume expansion and dextrose delivery as the solution is directly infused into the bloodstream.
Duration of ActionIntravenous: Short; dextrose effect on plasma glucose lasts 1-2 hours after infusion stops, while volume expansion from sodium chloride persists for 2-4 hours depending on renal function and distribution.
Molecular Weight180.156 (dextrose); 58.44 (sodium chloride)

Classification & Brands

Dosing & administration

Intravenous infusion; dosage depends on fluid and electrolyte requirements. Typical maintenance: 75-150 mL/kg/day for adults, administered as continuous infusion.

Dosage formINJECTABLE
Renal impairmentGFR >= 50 mL/min: no adjustment; GFR 30-49 mL/min: reduce total volume by 20-30% or use with caution; GFR <30 mL/min: avoid use due to risk of fluid overload and hypernatremia unless carefully monitored.
Liver impairmentChild-Pugh A: no adjustment; Child-Pugh B: monitor for fluid overload and electrolyte disturbances; Child-Pugh C: use with caution, reduce infusion rate and volume, may need diuretic therapy.
Pediatric useIntravenous infusion: neonates: 60-120 mL/kg/day; infants: 100-120 mL/kg/day; children: 75-100 mL/kg/day; adjust based on clinical status and serum electrolytes.
Geriatric useElderly patients may require reduced total volume and slower infusion rate due to decreased renal function and increased risk of fluid overload; monitor serum sodium, potassium, and fluid balance closely.

Use during pregnancy

1st trimesterDextrose and sodium chloride are essential nutrients; use is generally considered safe during pregnancy when administered for fluid and electrolyte maintenance. No known teratogenic effects.
2nd trimesterSafe for use in second trimester for hydration and electrolyte replacement. Monitor for fluid overload and electrolyte disturbances.
3rd trimesterSafe for use; however, caution in patients with preeclampsia or impaired renal function due to risk of fluid overload. May affect fetal glucose and sodium levels if maternal levels are abnormal.

Clinical note

No significant drug interactions Can cause hypernatremia and fluid overload.

FDA categoryAnimal
Placental transferBoth dextrose and sodium chloride freely cross the placenta by passive diffusion, achieving equilibrium with maternal concentrations. Fetal levels mirror maternal levels.
BreastfeedingDextrose and sodium chloride are normal components of breast milk. Intravenous administration is compatible with breastfeeding as the amounts transferred are negligible. No special precautions needed.
Lactation RatingL1 - Safe
Teratogenic RiskDextrose and sodium chloride are physiologic substances. No teratogenic risk has been identified at standard infusion rates. First trimester: No known risk. Second trimester: No known risk. Third trimester: Use caution to avoid fluid/electrolyte imbalance, which may affect fetal homeostasis.
Fetal MonitoringMonitor maternal serum electrolytes, blood glucose, fluid balance, and vital signs. Fetal monitoring should include heart rate and growth if prolonged administration occurs. Watch for maternal edema or hyperglycemia.
Fertility EffectsNo known adverse effects on fertility. Dextrose and sodium chloride are essential for cellular function and do not impair reproductive capacity at therapeutic doses.

Warnings & precautions

■ FDA Black Box Warning

None

Side Effect Profile

Common Effectsfluid replacement
Serious Effects

Absolute Contraindications

Hyperglycemia (for dextrose component)Hypernatremia (for sodium chloride component)Fluid overloadSevere renal impairment with oliguria

Clinical Precautions

PrecautionsRisk of hyperglycemia in patients with diabetes mellitus, Risk of fluid overload in patients with heart failure or renal impairment, Electrolyte imbalances with prolonged use, Do not administer if solution contains particulate matter or is discolored
Food/DietaryNo food interactions. May affect glucose control in diabetics; maintain consistent carbohydrate intake.

Clinical Tips & Counseling

Clinical PearlsUsed for maintenance fluid therapy; monitor for fluid overload in patients with CHF or renal impairment. Check serum glucose in diabetics as dextrose may cause hyperglycemia. Avoid in resuscitation due to hypotonicity.
Patient AdviceReport any swelling of hands, feet, or shortness of breath immediately. · If diabetic, monitor blood glucose closely. · This solution provides hydration and electrolytes; do not adjust infusion rate yourself.

DEXTROSE 2.5% AND SODIUM CHLORIDE 0.33% 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

ACETATED RINGER'S IN PLASTIC CONTAINERACYCLOVIR IN SODIUM CHLORIDE 0.9% PRESERVATIVE FREEAMIKACIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINERAMIKIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINERAMINOPHYLLINE IN SODIUM CHLORIDE 0.45%

External sources

DailyMed (NIH) PubMed OpenFDA