Enoxaparin Sodium (enoxaparin sodium)
Last reviewed · Source: First Databank (FDB) drug data
Overview
Enoxaparin, a low molecular weight heparin (LMWH) prepared by alkaline degradation of unfractionated benzylated heparin of porcine intestinal mucosa origin, is an anticoagulant.
Enoxaparin, a depolymerized heparin prepared by alkaline degradation of benzylated heparin of porcine intestinal mucosa origin, is an anticoagulant. Enoxaparin is commercially available as the sodium salt. The average molecular weight of enoxaparin is approximately one-third that of unfractionated heparin (4500 vs 12,000 daltons); therefore, enoxaparin is referred to as a low molecular weight heparin (LMWH).
Enoxaparin has an approximate anti-factor Xa activity of 100 units/mg according to the World Health Organization (WHO) First International Low Molecular Weight Heparin Reference Standard. At a given level of anti-factor Xa activity, enoxaparin has less effect on thrombin than does unfractionated heparin. However, enoxaparin administration has been associated with a prolongation of some global clotting function tests (i.e., thrombin time, activated partial thromboplastin time (aPTT)) by up to 1.8 times the control value.
In patients receiving enoxaparin sodium (1 mg/kg of the 100 mg/mL concentration subcutaneously every 12 hours) in a large clinical trial, the aPTT was 45 seconds or less in most treated patients. The manufacturer states that enoxaparin sodium in a concentration of 150 mg/mL is projected to produce anticoagulant activities similar to those of 100 or 200 mg/mL concentrations of the drug, although the 150 mg/mL concentration has not been studied clinically. Compared with unfractionated heparin, enoxaparin has greater bioavailability (based on anti-factor Xa activity) after subcutaneous administration and a longer half-life, allowing less frequent administration.
The molecular weight, pharmacokinetics, and in vitro and in vivo activity of enoxaparin differ from those of unfractionated heparin or other LMWHs; therefore, the drugs are not interchangeable on a unit-for-unit (or mg-for-mg) basis.
Enoxaparin is used for the prevention of venous thromboembolism (VTE) in patients undergoing orthopedic surgery or general (e.g., abdominal, gynecologic, urologic) surgery, and in medical patients with severely restricted mobility during acute illness. Enoxaparin also is used for the treatment of VTE in hospitalized patients with acute deep-vein thrombosis (DVT) with or without pulmonary embolism (PE) and in outpatients with acute DVT without accompanying PE.
Generic name: enoxaparin sodium
Pronunciation: (ee-NOX-a-PAR-in)
Reference product & biosimilars
No reference, biosimilar or interchangeable associated with this drug.
Today’s intelligence on Enoxaparin Sodium
Indications
The following indications are listed for Enoxaparin Sodium:
- Abdominal Surgery Deep Vein Thrombosis Prevention
- Acute St Elevation Myocardial Infarction
- Deep Vein Thrombosis Prevention
- Deep Vein Thrombosis With Pulmonary Embolism
- Deep Venous Thrombosis
- Hip Surgery Deep Vein Thrombosis Prevention
- Knee Replacement Deep Vein Thrombosis Prevention
- Prevention Of Cardiac Ischemia In Unstable Angina
- Prevention Of Ischemic Complications Of Non-Q Wave Mi
Also known as: Abdominal Surgery Dvt Prevention, Acute St Segment Elevation Mi, Acute Stemi, Deep Vein Thrombosis, Deep Vein Thrombosis Prophylaxis, Deep Vein Thrombosis Prophylaxis In Abdominal Surgery, Deep Vein Thrombosis Prophylaxis In Hip Surgery, Deep Vein Thrombosis Prophylaxis In Knee Replacement, Dvt Prevention, Hip Surgery Dvt Prevention, Knee Replacement Dvt Prevention, Prophylaxis For Cardiac Ischemia In Unstable Angina.
Dosing
Dosages for enoxaparin sodium or other low molecular weight heparins (LMWHs) or unfractionated heparin sodium cannot be used interchangeably on a unit-for-unit (or mg-for-mg) basis. Enoxaparin sodium has an approximate anti-factor Xa activity of 100 units/mg according to the World Health Organization (WHO) First International Low Molecular Weight Heparin Reference Standard.
If an LMWH is used for anticoagulation in children, ACCP suggests that dosage of the drug be adjusted to a target anti-factor Xa level of 0.5-1 units/mL based on a sample taken 4-6 hours, or 0.5-0.8 units/mL based on a sample taken 2-6 hours, following subcutaneous administration.
Enoxaparin sodium is administered by deep subcutaneous injection; it must not be given IM. The drug also is administered IV (as a direct IV injection) in certain situations. (See ST-Segment-Elevation Myocardial Infarction and also see Non-ST-Segment-Elevation Acute Coronary Syndrome under Dosage and Administration.)
Patients should be supine during administration of the drug.
To avoid loss of drug when using the prefilled syringes, the manufacturer states that air should not be expelled from the syringe prior to injection. If the prescribed dose is less than the full syringe volume, the excess syringe volume should be ejected until only the prescribed dose remains in the syringe.
No dosing information is available for this tab.
No dosing information is available for this tab.
Drug interactions
There is no enhanced messaging for this drug.
There are no contraindication interactions for this drug.
There are no severe interactions for this drug.
There are no moderate interactions for this drug.
Contraindications
*Active major bleeding.
*Immune-mediated heparin-induced thrombocytopenia within the prior 100 days or associated with circulating antiplatelet antibodies.
*Known hypersensitivity to enoxaparin sodium (e.g., pruritus, urticaria, anaphylactic/anaphylactoid reactions), heparin, pork products, benzyl alcohol, or any ingredient in the formulation.
There are no contraindication contraindications for this drug.
There are no severe contraindications for this drug.
There are no moderate contraindications for this drug.
Adverse reactions
The most common adverse effects of enoxaparin (i.e., occurring in at least 1% of patients receiving the drug in clinical studies) include bleeding, anemia, ecchymosis, thrombocytopenia, elevation of serum aminotransferase concentrations, fever, nausea, diarrhea, peripheral edema, dyspnea, injection site pain, and confusion.
There are no severe adverse reactions for this drug.
There are no less severe adverse reactions for this drug.
Precautions
No enhanced messaging available.
Safety and efficacy of enoxaparin have not been established in children younger than 18 years of age.
Each mL of enoxaparin sodium injection in multiple-dose vials contains 15 mg of benzyl alcohol as a preservative. Although a causal relationship has not been established, administration of injections preserved with benzyl alcohol has been associated with toxicity in neonates, including fatal reactions and the ''gasping syndrome''. Toxicity appears to have resulted from administration of large amounts (i.e., about 100-400 mg/kg daily) of benzyl alcohol in these neonates. Because benzyl alcohol may cross the placenta, the manufacturer states that the preservative-free formulations of enoxaparin should be used in pregnant women whenever possible.
There are no adequate and well-controlled studies of enoxaparin in pregnant women. Animal studies indicate that enoxaparin crosses the placenta; however, available data in humans indicate that low molecular weight heparins (LMWHs) do not cross the placenta. Available human data also have not shown evidence of teratogenicity or fetotoxicity. In a review of approximately 600 retrospectively followed pregnancies in women exposed to enoxaparin, the incidences of congenital anomalies did not exceed what would be expected in the general population. Maternal and neonatal hemorrhage did occur in some of the followed pregnancies. The American College of Obstetricians and Gynecologists (ACOG) considers LMWHs to be generally safe in pregnancy.
Pregnancy alone is associated with an increased risk of thromboembolism, which is even higher in women with a history of thromboembolism and certain high-risk pregnancy conditions, including hereditary or acquired thrombophilias and the presence of a mechanical prosthetic heart valve. The pharmacokinetics of LMWHs differ in pregnant versus nonpregnant women because of changes in volume of distribution resulting in increased plasma volume, decreased half-life, and changes in renal clearance. Some clinicians recommend frequent monitoring of anti-factor Xa concentrations and adjustment of enoxaparin sodium dosage in pregnant women with mechanical prosthetic heart valves to ensure a consistent anticoagulant effect.
All patients receiving anticoagulants such as enoxaparin, including pregnant women, are at risk for bleeding. Hemorrhage can occur at any site and may lead to death of mother and/or fetus. Pregnant women receiving enoxaparin should be apprised of the potential hazards to the mother and fetus associated with enoxaparin use during pregnancy, and such women should be carefully monitored for evidence of bleeding or excessive anticoagulation. Use of enoxaparin may result in epidural or spinal hematomas in women receiving neuraxial anesthesia during labor and delivery. Pregnant women receiving enoxaparin should be monitored for bleeding and for any unexpected changes in coagulation parameters. As delivery approaches, use of a shorter-acting anticoagulant should be considered.
Use of enoxaparin in pregnant women with mechanical prosthetic heart valves may result in valve thrombosis. (See Patients with Mechanical Prosthetic Heart Valves under Cautions.)
It is not known whether enoxaparin is distributed into milk; studies in lactating rats demonstrated very limited distribution of enoxaparin into milk. It is not known whether enoxaparin affects the breast-fed child or affects milk production. The benefits of breast-feeding should be considered along with the importance of the drug to the woman and any potential adverse effects on the breast-fed child from the drug or underlying maternal condition.
The American College of Obstetricians and Gynecologists (ACOG) considers low molecular weight heparins (LMWHs) to be compatible with lactation. The American College of Chest Physicians (ACCP) recommends that LMWHs be continued in nursing women who are already receiving such therapy; the small amounts of drug detected in the milk of nursing women are not likely to be clinically important.
No substantial differences in efficacy have been observed in geriatric patients relative to younger adults. In geriatric patients, a higher incidence of bleeding complications has been observed following administration of enoxaparin sodium at a dosage of 1.5 mg/kg once daily or 1 mg/kg every 12 hours, and the risk of bleeding complications increases with age. Enoxaparin should be used with care in geriatric patients, and careful attention to dosing intervals and concomitant medications (particularly antiplatelet drugs) is advised. Monitoring (e.g., using anti-factor Xa assay) of geriatric patients with low body weight (<45 kg) and those predisposed to decreased renal function should be considered.
ICD codes
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Last reviewed · Source: First Databank (FDB) drug data
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