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Electrolyte/Discontinued

HEPARIN SODIUM 5,000 UNITS IN SODIUM CHLORIDE 0.45%

HEPARIN SODIUM 5,000 UNITS IN SODIUM CHLORIDE 0.45%

Clinical safety rating

safe

No significant drug interactions Can cause hypernatremia and fluid overload.


Mechanism of Action

Heparin binds to antithrombin III, causing a conformational change that accelerates the inhibition of thrombin and activated factor X (factor Xa). It also catalyzes the inhibition of other coagulation factors including XIIa, XIa, IXa, and VIIa.

What the body does with it

MetabolismHeparin is partially metabolized by the reticuloendothelial system and desulfated. Clearance is dose-dependent and saturable, primarily via the liver (heparinase) and to a lesser extent renal excretion.
ExcretionPrimarily renal, with some hepatic metabolism and reticuloendothelial system clearance. Unchanged heparin is excreted in urine via glomerular filtration; high molecular weight fractions are cleared more rapidly than low molecular weight fractions.
Half-lifeMean terminal elimination half-life is 1-2 hours at therapeutic doses, but it is dose-dependent and can increase with higher doses. Clinical context: Anticoagulant effect persists longer than plasma levels due to irreversible binding to antithrombin III.
Protein bindingVery high; ~95% bound primarily to antithrombin III, with some binding to albumin and other proteins.
Volume of Distribution0.05-0.07 L/kg (approximately 4-5 L in adults). Clinical meaning: Low Vd indicates predominantly intravascular distribution; heparin does not cross the placenta or blood-brain barrier.
BioavailabilitySubcutaneous: 20-30% (due to first-pass metabolism and binding); Intravenous: 100%.
Onset of ActionIntravenous: Immediate. Subcutaneous: 20-30 minutes.
Duration of ActionIntravenous: 2-6 hours (dose-dependent). Subcutaneous: 8-12 hours (prolonged with higher doses). Clinical note: Effect monitored via aPTT; prolonged use may require dose adjustment.
Molecular Weight12000

Classification & Brands

Dosing & administration

IV: Initial bolus 80 units/kg, then continuous infusion at 18 units/kg/hr, adjusted to aPTT 1.5-2.5 times control. Subcutaneous: 5,000 units every 8-12 hours.

Dosage formINJECTABLE
Renal impairmentCrCl <30 mL/min: Reduce infusion rate by 50% or consider alternative. Monitor aPTT closely.
Liver impairmentChild-Pugh Class B or C: Reduce dose by 50% due to decreased clearance; monitor aPTT.
Pediatric useIV bolus 75-100 units/kg, then infusion: Infants <1 year: 28 units/kg/hr; Children >1 year: 20 units/kg/hr; adjust to aPTT 60-85 seconds.
Geriatric useReduce initial bolus to 50-60 units/kg and infusion rate to 15 units/kg/hr due to altered clearance; frequent aPTT monitoring.

Use during pregnancy

1st trimesterHeparin does not cross the placenta due to high molecular weight and is not associated with teratogenic risk. Use is considered safe when clinically indicated.
2nd trimesterNo increased risk of fetal harm; continued use is acceptable for maternal thromboembolic disorders.
3rd trimesterRisk of maternal hemorrhage and osteoporosis with prolonged use; monitoring recommended. No fetal anticoagulation.

Clinical note

No significant drug interactions Can cause hypernatremia and fluid overload.

FDA categoryAnimal
Placental transferDoes not cross the placenta due to molecular weight >20,000 Da and negative charge.
BreastfeedingHeparin is not excreted into breast milk due to its high molecular weight and ionization, making it incompatible with milk transfer. Use is considered compatible with breastfeeding.
Lactation RatingL1 (Safest)
Teratogenic RiskHeparin does not cross the placenta; no known teratogenic effects in any trimester. Risk of maternal hemorrhage and fetal bleeding during delivery.
Fetal MonitoringMonitor maternal aPTT, platelet count, and signs of bleeding. Fetal surveillance not required; monitor for signs of placental abruption or hemorrhage.
Fertility EffectsNo known adverse effects on human fertility based on available data.

Warnings & precautions

■ FDA Black Box Warning

Heparin is contraindicated in patients with a history of heparin-induced thrombocytopenia (HIT). Fatal hemorrhages have occurred. Monitor platelets closely.

Side Effect Profile

Common Effectsfluid replacement
Serious Effects

Absolute Contraindications

Severe thrombocytopenia (heparin-induced thrombocytopenia, HIT)Uncontrolled active bleeding (except when due to disseminated intravascular coagulation)Known hypersensitivity to heparin or pork productsInability to perform appropriate monitoring (e.g., aPTT)

Clinical Precautions

PrecautionsRisk of hemorrhage: Monitor for bleeding, especially in patients with predisposing factors (e.g., renal failure, recent surgery)., Heparin-induced thrombocytopenia (HIT): Monitor platelet counts regularly; discontinue if HIT is suspected., Heparin-induced thrombocytopenia with thrombosis (HITT): May require alternative anticoagulation., Osteoporosis: Long-term use may lead to bone density loss., Hyperkalemia: Heparin may suppress adrenal aldosterone secretion, leading to hyperkalemia, especially in renal impairment or diabetes., Heparin resistance: May occur in antithrombin III deficiency or elevated heparin clearance.
Food/DietaryNo clinically significant food interactions with heparin flushes. No dietary restrictions required for this indication.

Clinical Tips & Counseling

Clinical PearlsHEPARIN SODIUM 5,000 UNITS IN SODIUM CHLORIDE 0.45% is a fixed-dose formulation used for venous access device flushing to maintain patency. Not for systemic anticoagulation. Verify catheter size and type to ensure appropriate flush volume. Avoid in patients with heparin-induced thrombocytopenia (HIT). Use preservative-free formulation in neonates. Monitor for signs of bleeding or hypersensitivity. Do not expel air from syringe to avoid air embolism; instead use proper priming technique.
Patient AdviceThis medication is used to keep your IV or catheter line clear and prevent blood clots inside it. · It is a very small dose of heparin; it does not thin your blood throughout your body. · Report any unusual bleeding, bruising, or pain at the IV site to your healthcare provider. · Tell your doctor if you have ever had a reaction to heparin or a history of low platelet counts with heparin use. · Do not use this medication if you have active bleeding or a bleeding disorder. · Store at room temperature away from light and moisture.

HEPARIN SODIUM 5,000 UNITS IN SODIUM CHLORIDE 0.45% 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