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Electrolyte/Discontinued

INULIN AND SODIUM CHLORIDE

INULIN AND SODIUM CHLORIDE

Clinical safety rating

safe

No significant drug interactions Can cause hypernatremia and fluid overload.


Mechanism of Action

Inulin is a polysaccharide that is not absorbed from the gastrointestinal tract and is used as a diagnostic agent to measure glomerular filtration rate (GFR) by renal clearance. Sodium chloride provides electrolyte supplementation.

What the body does with it

MetabolismInulin is not metabolized; it is excreted unchanged by the kidneys. Sodium chloride is absorbed and distributed; no metabolism.
ExcretionRenal: 100% as unchanged drug via glomerular filtration without tubular reabsorption or secretion; biliary/fecal: negligible (<1%)
Half-lifeNormal renal function: 1.5 hours (range 1–2 h); decreases to 0.5 h with severe renal impairment; used to measure glomerular filtration rate (GFR)
Protein bindingApproximately 0% (negligible); does not bind to plasma proteins
Volume of Distribution0.15–0.25 L/kg (approx. 15–25% of body weight; confined to extracellular fluid); reflects distribution limited to extracellular space
BioavailabilityIntravenous: 100%; oral: <1% (not absorbed; used for oral GFR measurement but bioavailability is negligible)
Onset of ActionIntravenous: immediate (within minutes) after injection; oral: not applicable (no clinical effect used only as diagnostic agent)
Duration of ActionIntravenous: 1–2 hours (clearance from plasma); persists until renal excretion complete; prolonged in renal impairment
Molecular Weight504.44

Classification & Brands

Dosing & administration

Inulin: 5 g IV bolus followed by continuous infusion at 1.5 mL/min of a 10 g/L solution for GFR measurement. Sodium chloride: 0.9% solution as diluent.

Dosage formINJECTABLE
Renal impairmentInulin excretion is renal; no dose adjustment as used for GFR measurement. In renal failure, monitor for hypernatremia from NaCl content.
Liver impairmentNo specific adjustment required; inulin is not hepatically metabolized.
Pediatric useInulin: 0.5 mL/kg IV bolus of 10% solution followed by infusion at 0.15 mL/kg/min. Sodium chloride: as per isotonic requirement.
Geriatric useUse standard dosing; consider reduced GFR in elderly; monitor volume and electrolyte status.

Use during pregnancy

1st trimesterInulin is not absorbed orally; it is a non-digestible fructan. No known teratogenic risk. Sodium chloride should be used with caution if there is a need for sodium restriction. Overall, likely safe when used as a diagnostic agent (inulin IV for GFR measurement) but only if clearly needed.
2nd trimesterSame as T1. Inulin is not metabolized and is excreted unchanged by glomerular filtration. No adverse fetal effects reported.
3rd trimesterSame as T1. Consider maternal fluid and electrolyte balance.

Clinical note

No significant drug interactions Can cause hypernatremia and fluid overload.

FDA categoryAnimal
Placental transferInulin is a polysaccharide with very low lipid solubility; placental transfer is negligible. Sodium and chloride ions cross the placenta via active transport and are regulated; no specific concern.
BreastfeedingInulin is not absorbed orally and is unlikely to appear in breast milk. Sodium chloride is a normal component of breast milk; additional intake from maternal diet or IV administration is not expected to cause harm. However, if given intravenously for diagnostic purposes, use minimal necessary dose.
Lactation RatingL1 (Safest)
Teratogenic RiskInulin is not absorbed systemically; sodium chloride is physiologic. No known teratogenic risk in any trimester.
Fetal MonitoringMonitor fluid balance, electrolytes, renal function during prolonged use; fetal assessment not specifically required.
Fertility EffectsNo known effects on human fertility.

Warnings & precautions

■ FDA Black Box Warning

No FDA black box warning.

Side Effect Profile

Common Effectsfluid replacement
Serious Effects

Absolute Contraindications

Hypersensitivity to inulin or any component of the formulationSevere hypernatremia or fluid overload (if using sodium chloride-containing solution)

Clinical Precautions

PrecautionsUse with caution in patients with known anuria or severe renal impairment due to risk of accumulation. Monitor fluid and electrolyte balance.
Food/DietaryNo specific food interactions. Maintain adequate hydration as directed. Avoid excessive salt intake if sodium chloride load is a concern.

Clinical Tips & Counseling

Clinical PearlsInulin is an inert polysaccharide used in glomerular filtration rate (GFR) measurement. Administer as a continuous IV infusion to maintain steady-state plasma levels. Avoid extravasation; inulin is non-irritating but high volumes may cause discomfort. Monitor for fluid overload in patients with compromised cardiac function due to sodium chloride content. Use isotonic (0.9%) or half-isotonic solution depending on hydration status.
Patient AdviceYou will receive a solution containing inulin and salt through a vein to test your kidney function. · Report any pain, redness, or swelling at the IV site. · You may experience a metallic taste or warmth during infusion; these are temporary. · Stay well hydrated before and after the test unless advised otherwise.

INULIN AND SODIUM CHLORIDE 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