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Electrolyte/Discontinued

SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

Clinical safety rating

safe

No significant drug interactions Can cause hypernatremia and fluid overload.


Mechanism of Action

Sodium chloride 0.45% (half-normal saline) is an isotonic crystalloid solution that provides sodium and chloride ions to maintain or restore extracellular fluid volume. It expands intravascular volume, corrects electrolyte imbalances, and can dilute plasma osmolality. The chloride component helps maintain acid-base balance.

What the body does with it

MetabolismSodium and chloride are not metabolized; they are excreted primarily by the kidneys. No hepatic metabolism.
ExcretionRenal: >90% as sodium and chloride ions; negligible biliary/fecal elimination.
Half-lifeNot applicable; sodium and chloride ions are endogenous substances with rapid renal regulation; no defined half-life.
Protein bindingNegligible (<5%); sodium and chloride are free ions.
Volume of DistributionSodium: 0.6-0.7 L/kg (total body water); chloride distribution similar. Clinically, distributes throughout extracellular fluid.
BioavailabilityIV: 100%; not administered orally as hypotonic solution; oral: negligible due to osmotic effects and gastrointestinal regulation.
Onset of ActionIV: Rapid (minutes) for volume expansion and electrolyte correction.
Duration of ActionIV: 1-2 hours for volume expansion; depends on renal function and hydration status.
Molecular Weight58.44

Classification & Brands

Dosing & administration

Intravenous; adult: 500-1000 mL at a rate of 50-100 mL/hour (maintenance); adjust based on fluid and electrolyte status.

Dosage formINJECTABLE
Renal impairmentNo specific dose adjustment; monitor serum electrolytes and fluid balance; use with caution in severe renal impairment due to risk of hypernatremia.
Liver impairmentNo specific dose adjustment; monitor serum sodium in ascites or edema.
Pediatric useIntravenous; weight-based: 20-100 mL/kg/day (maintenance); rate adjusted based on age, weight, and clinical condition.
Geriatric useConsider reduced initial rate due to potential for fluid overload; monitor cardiovascular and renal function closely.

Use during pregnancy

1st trimesterSafe in pregnancy; used as vehicle for IV medications or to correct dehydration/hyponatremia. No known teratogenicity at therapeutic doses.
2nd trimesterSafe; same as t1. Monitor serum sodium and volume status in prolonged use.
3rd trimesterSafe; same as t1 and t2. Caution in preeclampsia or heart failure due to fluid overload risk.

Clinical note

No significant drug interactions Can cause hypernatremia and fluid overload.

FDA categoryAnimal
Placental transferSodium and chloride freely cross the placenta via passive diffusion and active transport; concentrations in fetal blood are regulated by maternal levels and placental function.
BreastfeedingSodium chloride infusions are compatible with breastfeeding as sodium and chloride are normal milk constituents. Avoid excessive doses that may alter maternal plasma sodium; minimal transfer to milk.
Lactation RatingL1
Teratogenic RiskNo known teratogenic risk; sodium chloride is a normal constituent of body fluids and is not associated with fetal harm at standard doses. There is no evidence of teratogenicity in any trimester.
Fetal MonitoringMonitor maternal serum electrolytes (sodium, chloride) and fluid balance, especially in prolonged infusion or compromised renal function. Fetal monitoring is not routinely required unless maternal complications arise.
Fertility EffectsNo known adverse effects on fertility. Sodium chloride at physiological concentrations does not impair reproductive function.

Warnings & precautions

■ FDA Black Box Warning

None.

Side Effect Profile

Common Effectsfluid replacement
Serious Effects

Absolute Contraindications

HypernatremiaFluid overload states (e.g., heart failure, pulmonary edema)Severe renal impairment with oliguria/anuria

Clinical Precautions

PrecautionsMonitor serum electrolytes, renal function, and fluid status during prolonged therapy, Risk of fluid overload in patients with heart failure, renal impairment, or edema, Infusion rate should be adjusted based on clinical condition and lab values, Use with caution in patients with hypertension or hypernatremia, May cause hyperchloremic metabolic acidosis if large volumes are administered rapidly
Food/DietaryNone specific. However, monitor dietary salt intake if receiving concurrent IV sodium. Avoid excessive oral sodium consumption during treatment.

Clinical Tips & Counseling

Clinical Pearls0.45% sodium chloride is a hypotonic solution used for maintenance fluid therapy or to treat hypernatremia. Avoid in patients with increased intracranial pressure due to risk of cerebral edema. Monitor serum sodium frequently to prevent rapid correction. Use with caution in patients with heart failure or renal impairment.
Patient AdviceThis fluid is given intravenously to restore body water and salt levels. · Tell your healthcare provider if you have heart, kidney, or liver disease. · Report any swelling, shortness of breath, or headache promptly. · Do not stop the infusion without medical advice.

SODIUM CHLORIDE 0.45% 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