Overview

Enoxaparin is a low molecular weight heparin manufactured by Sanofi-Aventis. It is marketed as Lovenox or Clexane. Enoxaparin injections are derived from the intestinal mucosa of pigs. Enoxaparin is used to prevent and treat deep vein thrombosis or pulmonary embolism, and is given as a subcutaneous injection (by a health care provider or the patient). Its use is evolving in acute coronary syndromes (ACS).

Indications

In the United Kingdom, enoxaparin is approved for five indications:

The prophylaxis of thromboembolism disorders of venous origin, in particular those which may be associated with orthopaedic surgery.
The prophylaxis of venous thromboembolism (VTE) in medical patients bedridden due to acute illness.
The treatment of venous thromboembolism disease (VTED) presenting with deep vein thrombosis (DVT), pulmonary embolism (PE) or both.
The treatment of unstable angina (UA) and non-Q-wave myocardial infarction (NQMI), administered concurrently with aspirin.
The prevention of thrombus formation in the extracorporeal circulation during haemodialysis.

In the United States, enoxaparin is FDA approved for eight indications:

Prophylaxis of DVT in medically ill patient,
Total hip & knee replacement,
Extended hip-replacement,
Abdominal surgery.
Treatment of DVT with or with out PE inpatient and
Treatment of DVT inpatient, with ACS, including STEMI.

Mechanism of action

Enoxaparin binds to and accelerates the activity of antithrombin III. By activating antithrombin III, enoxaparin preferentially potentiates the inhibition of coagulation factors Xa and IIa. The anticoagulant effect of enoxaparin can be directly correlated to its ability to inhibit factor Xa. Factor Xa catalyzes the conversion of prothrombin to thrombin, so enoxaparin’s inhibition of this process results in decreased thrombin and ultimately the prevention of fibrin clot formation.

Monitoring

Enoxaparin detailed information
Clinical data
Pregnancy; category	B;
Routes of; administration	Subcutaneous (SC) Injection and intervenous (IV) per package insert
ATC code	B01AB05 (WHO) ;
Pharmacokinetic data
Bioavailability	92%
Protein binding	80% bound-albumin
Metabolism	primarily by liver by desulfation and/or depolymerization
Elimination half-life	4.5 hours
Identifiers
	IUPAC name 6-[5-acetylamino-4,6-dihydroxy-2- (sulfooxymethyl)tetrahydropyran-3-yl] oxy-3- [5-(6-carboxy-4,5-dihydroxy-3- sulfooxy-tetrahydropyran-2-yl)oxy-6-(hydroxymethyl)- 3-sulfoamino-4-sulfooxy-tetrahydropyran-2-yl] oxy-4-hydroxy-5-sulfooxy-tetrahydropyran-2- carboxylicacid;
CAS Number	9005-49-6;
PubChem CID	772;
DrugBank	APRD00068;
E number	{{#property:P628}}
ECHA InfoCard	{{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
Formula	(C26H40N2O36S5)n
Molar mass	4500 daltons (average)

Enoxaparin does not affect the INR, PT or aPTT
Anti-factor Xa levels can be measured, and are often used to monitor enoxaparin activity

Pregnancy

Category B: enoxaprin is safe for use in the second trimester as it does not cross the placenta

Side effects

Bleeding
Thrombocytopenia, i.e. can be associated with heparin-induced thrombocytopenia
Pain, bruising or irritation; hard, inflamed nodules or an itchy red rash at the injection site
Symptoms similar to those of hayfever
Abdominal/chest pain
Headache

Reversal Agent

Protamine, although not as effective at reversal as it is for heparin due to more activity at the Xa clotting factor (enoxaparin); as heparin has both Xa and IIa. Protamine sulfate will reverse enoxaparin by 66% per package insert.

Availability

100 mg/mL

Prefilled Syringes: 30mg/0.3mL, 40mg/0.4mL
Graduated Prefilled Syringes: 60mg/0.6mL, 80mg/0.8mL, 100mg/1mL
Multiple Dose Vials: 300mg/3.0mL

150mg/mL

Graduated Prefilled Syringes: 120mg/0.8mL, 150mg/1mL

External links

Template:WikiDoc Sources

Enoxaparin detailed information

Contents