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HEPARIN SODIUM 1,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

HEPARIN SODIUM 1,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

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 inactivation of thrombin (factor IIa) and activated factor X (factor Xa), thereby inhibiting coagulation.

What the body does with it

MetabolismHeparin is primarily cleared via the reticuloendothelial system and undergoes desulfation and depolymerization. A portion is excreted unchanged in urine.
ExcretionRenal: Heparin is primarily cleared by the reticuloendothelial system and the liver via desulfation and depolymerization, with metabolites excreted in urine. Only about 50% of an administered dose is excreted unchanged in urine at therapeutic doses; the remainder is metabolized. Biliary/fecal excretion is minimal.
Half-lifeTerminal elimination half-life is dose-dependent: 0.5–1.5 hours after intravenous administration of 100 U/kg, increasing to 1.5–2.5 hours after 200 U/kg, and up to 3–6 hours after 400 U/kg. Clinically, the anticoagulant effect (aPTT) has a half-life of approximately 1–2 hours, and this is used for dosing adjustments.
Protein bindingHeparin binds extensively to various plasma proteins, including antithrombin III (high affinity), albumin, and other proteins. Overall protein binding is approximately 95%.
Volume of Distribution0.06–0.07 L/kg (low, as heparin is largely confined to the intravascular space).
BioavailabilitySubcutaneous: approximately 30–40% (low due to poor absorption and metabolism at injection site). Intravenous: 100%.
Onset of ActionIntravenous: immediate (within minutes). Subcutaneous: 1–2 hours (with a lag of 1 hour).
Duration of ActionIntravenous: 2–6 hours (dose-dependent; effect monitored via aPTT). Subcutaneous: 8–12 hours (requires twice-daily dosing for therapeutic anticoagulation).
Molecular Weight12000-15000 Da (unfractionated heparin average ~15000 Da; low molecular weight derivatives ~4000-6000 Da, but UFH is the typical formulation in this product)

Classification & Brands

Dosing & administration

Adult: IV bolus 5,000 units followed by continuous IV infusion at 1,000 units/hour (25,000-40,000 units/24h) titrated to aPTT 1.5-2.5 times control. Subcutaneous: 5,000 units every 8-12 hours.

Dosage formINJECTABLE
Renal impairmentNo specific GFR-based dose adjustment required; monitor aPTT. In severe renal impairment (CrCl <30 mL/min), reduce infusion rate by 20-50% and monitor anti-Xa levels.
Liver impairmentChild-Pugh Class A: No adjustment. Child-Pugh Class B: Reduce dose by 25-50% with close aPTT monitoring. Child-Pugh Class C: Avoid or use with extreme caution; reduce dose by 50-75%.
Pediatric useIV bolus: 50-100 units/kg, then continuous IV infusion: 15-25 units/kg/hour. Titrate to aPTT 60-85 seconds or anti-Xa 0.3-0.7 units/mL.
Geriatric useElderly patients may have reduced clearance; use lower initial infusion rates (e.g., 750 units/hour) and monitor aPTT frequently. Start with 50% of the usual bolus dose in patients >70 years.

Use during pregnancy

1st trimesterHeparin does not cross the placenta; no known teratogenic effects in animal studies. Limited human data, but considered safe when indicated.
2nd trimesterNo evidence of fetal harm; continues to be safe for anticoagulation when needed.
3rd trimesterUse with caution near term due to risk of maternal hemorrhage; monitor coagulation parameters.

Clinical note

No significant drug interactions Can cause hypernatremia and fluid overload.

FDA categoryAnimal
Placental transferNone; heparin does not cross the placenta due to its large molecular size and negative charge.
BreastfeedingHeparin is not excreted into breast milk due to its high molecular weight and poor oral bioavailability, making it safe during breastfeeding. No adverse effects reported in nursing infants.
Lactation RatingL1 (Safe)
Teratogenic RiskHeparin is not known to cross the placenta due to its high molecular weight and negative charge, and is not associated with fetal teratogenicity. First trimester: No increased risk of major malformations. Second and third trimesters: No known teratogenic effects; use for treatment or prevention of thrombosis is considered safe. Risk of maternal hemorrhage and placental abruption exists with overdose.
Fetal MonitoringMonitor maternal platelet counts (risk of heparin-induced thrombocytopenia, HIT), activated partial thromboplastin time (aPTT) to maintain therapeutic range (1.5-2.5 times control), signs of bleeding (ecchymosis, hematuria, gastrointestinal bleeding), and fetal surveillance (ultrasound for growth and placental assessment if used for antiphospholipid syndrome or thrombosis).
Fertility EffectsHeparin is not known to impair fertility. It is used in assisted reproductive technology for thromboprophylaxis without adverse effects on fertility outcomes.

Warnings & precautions

■ FDA Black Box Warning

Heparin is not intended for intramuscular use due to risk of hematoma. Monitor for signs of bleeding, especially in patients with risk factors. Epidural or spinal hematomas may occur with concurrent neuraxial anesthesia or spinal puncture, resulting in long-term or permanent paralysis.

Side Effect Profile

Common Effectsfluid replacement
Serious Effects

Absolute Contraindications

History of heparin-induced thrombocytopenia (HIT)Active major bleeding or hemorrhagic disordersSevere thrombocytopenia (platelet count <50,000/μL)Known hypersensitivity to heparin or pork productsInability to perform adequate coagulation monitoring

Clinical Precautions

PrecautionsRisk of hemorrhage: monitor coagulation parameters (aPTT) and adjust dose accordingly., Heparin-induced thrombocytopenia (HIT): monitor platelet counts; discontinue if HIT suspected., Hyperkalemia: heparin suppresses aldosterone synthesis; monitor potassium in high-risk patients., Osteoporosis with long-term use ( >3 months)., Use with caution in patients with severe hepatic or renal impairment, uncontrolled hypertension, or history of gastrointestinal ulcers.
Food/DietaryNo significant food interactions. However, avoid excessive alcohol consumption as it may increase bleeding risk. Vitamin K-rich foods (e.g., leafy greens) do not affect heparin's anticoagulant effect, in contrast to warfarin.

Clinical Tips & Counseling

Clinical PearlsUse actual body weight for dosing; check aPTT 6 hours after initiation and after dose changes; monitor platelet count for heparin-induced thrombocytopenia (HIT); avoid intramuscular injections during therapy. Protamine sulfate (1 mg per 100 units heparin) reverses effects. For I.V. flushes, use preservative-free formulation when possible.
Patient AdviceReport any unusual bleeding or bruising immediately. · Avoid aspirin, NSAIDs, and other blood thinners unless prescribed. · Inform all healthcare providers (including dentists) that you are on heparin. · Do not take any new medications without consulting your doctor. · Seek medical help if you experience signs of allergic reaction (rash, itching, swelling, severe dizziness, trouble breathing).

HEPARIN SODIUM 1,000 UNITS IN SODIUM CHLORIDE 0.9% 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

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External sources

DailyMed (NIH) PubMed OpenFDA