MedPath

Heparin

Generic Name
Heparin
Brand Names
Heparin Leo
Drug Type
Small Molecule
CAS Number
9005-49-6
Unique Ingredient Identifier
T2410KM04A

Overview

Unfractionated heparin (UH) is a heterogenous preparation of anionic, sulfated glycosaminoglycan polymers with weights ranging from 3000 to 30,000 Da. It is a naturally occurring anticoagulant released from mast cells. It binds reversibly to antithrombin III (ATIII) and greatly accelerates the rate at which ATIII inactivates coagulation enzymes thrombin (factor IIa) and factor Xa. UH is different from low molecular weight heparin (LMWH) in the following ways: the average molecular weight of LMWH is about 4.5 kDa whereas it is 15 kDa for UH; UH requires continuous infusions; activated partial prothrombin time (aPTT) monitoring is required when using UH; and UH has a higher risk of bleeding and higher risk of osteoporosis in long term use. Unfractionated heparin is more specific than LMWH for thrombin. Furthermore, the effects of UH can typically be reversed by using protamine sulfate.

Background

Unfractionated heparin (UH) is a heterogenous preparation of anionic, sulfated glycosaminoglycan polymers with weights ranging from 3000 to 30,000 Da. It is a naturally occurring anticoagulant released from mast cells. It binds reversibly to antithrombin III (ATIII) and greatly accelerates the rate at which ATIII inactivates coagulation enzymes thrombin (factor IIa) and factor Xa. UH is different from low molecular weight heparin (LMWH) in the following ways: the average molecular weight of LMWH is about 4.5 kDa whereas it is 15 kDa for UH; UH requires continuous infusions; activated partial prothrombin time (aPTT) monitoring is required when using UH; and UH has a higher risk of bleeding and higher risk of osteoporosis in long term use. Unfractionated heparin is more specific than LMWH for thrombin. Furthermore, the effects of UH can typically be reversed by using protamine sulfate.

Indication

Unfractionated heparin is indicated for prophylaxis and treatment of venous thrombosis and its extension, prevention of post-operative deep venous thrombosis and pulmonary embolism and prevention of clotting in arterial and cardiac surgery. In cardiology, it is used to prevent embolisms in patients with atrial fibrillation and as an adjunct antithrombin therapy in patients with unstable angina and/or non-Q wave myocardial infarctions (i.e. non-ST elevated acute coronary artery syndrome) who are on platelet glycoprotein (IIb/IIIa) receptor inhibitors. Additionally, it is used to prevent clotting during dialysis and surgical procedures, maintain the patency of intravenous injection devices and prevent in vitro coagulation of blood transfusions and in blood samples drawn for laboratory values.

Associated Conditions

  • Blunt Injury
  • Clotting
  • Coagulopathy, Consumption
  • Contusions
  • Deep vein thrombosis postoperative
  • Disseminated Intravascular Coagulation (DIC)
  • External Hemorrhoid
  • Inflammation
  • Inflammatory, non-infectious pruritic dermatosis
  • Interstitial Cystitis
  • Post procedural pulmonary embolism
  • Pulmonary Embolism
  • ST Segment Elevation Myocardial Infarction (STEMI)
  • Sprains
  • Thromboembolism
  • Unstable Angina Pectoris
  • Venous Thrombosis (Disorder)
  • Hematomas
  • Peripheral arterial embolism
  • Thromboembolic phenomena
  • Varicosities of the great saphenous vein

FDA Approved Products

Heparin Sodium
Manufacturer:McKesson Corporation dba SKY Packaging
Route:INTRAVENOUS, SUBCUTANEOUS
Strength:1000 [USP'U] in 1 mL
Approved: 2023/08/30
NDC:63739-900
Heparin Sodium
Manufacturer:Hikma Pharmaceuticals USA Inc.
Route:INTRAVENOUS, SUBCUTANEOUS
Strength:5000 [USP'U] in 1 mL
Approved: 2022/12/12
NDC:0641-6199
Heparin Sodium
Manufacturer:Cardinal Health 107, LLC
Route:INTRAVENOUS, SUBCUTANEOUS
Strength:5000 [USP'U] in 1 mL
Approved: 2021/04/28
NDC:55154-9585
HEPARIN SODIUM
Manufacturer:HF Acquisition Co LLC, DBA HealthFirst
Route:INTRAVENOUS, SUBCUTANEOUS
Strength:10000 [USP'U] in 1 mL
Approved: 2024/01/29
NDC:51662-1409
Heparin Sodium
Manufacturer:NorthStar RxLLC
Route:INTRAVENOUS, SUBCUTANEOUS
Strength:2000 [USP'U] in 2 mL
Approved: 2024/01/19
NDC:72603-336

Singapore Approved Products

HEPARIN INJECTION 1,000 iu/ml
Manufacturer:LEO Pharma A/S
Form:INJECTION
Strength:1000 iu/ml
Online:Yes
Approved: 1988/05/03
Approval:SIN00720P
DBL HEPARIN SODIUM INJECTION BP (PORCINE) 1,000 iu/ml
Manufacturer:Siegfried Hameln GmbH
Form:INJECTION
Strength:1000 iu/ml
Online:Yes
Approved: 1988/06/13
Approval:SIN01768P
HEPARINISED SALINE INJECTION 10 iu/ml
Manufacturer:B BRAUN MEDICAL INDUSTRIES SDN BHD
Form:INJECTION
Strength:10 iu/ml
Online:Yes
Approved: 2003/04/04
Approval:SIN12253P
HEPARIN INJECTION 5,000 iu/ml
Manufacturer:LEO Pharma A/S
Form:INJECTION
Strength:5000 iu/ml
Online:Yes
Approved: 1988/05/03
Approval:SIN00714P
DBL HEPARIN SODIUM INJECTION BP (PORCINE) 5,000 iu/ml
Manufacturer:Siegfried Hameln GmbH
Form:INJECTION
Strength:5000 iu/ml
Online:Yes
Approved: 1988/06/13
Approval:SIN01766P

Drug Development Updates

Stay informed with timely notifications on clinical trials and research advancements.

© Copyright 2025. All Rights Reserved by MedPath