Abciximab: Difference between revisions
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==Mechanism of Action== | ==Mechanism of Action== | ||
Abciximab is a chimeric human-murine monoclonal antibody Fab fragment which inhibits platelet aggregation by binding to the glycoprotein IIb/IIIa receptors on platelets. It prevents [[fibrinogen]] and [[von Willebrand factor]] from binding to the receptor in a dose-dependent manner. Abciximab may also bind to the [[vitronectin]] receptor and to the [[Mac-1]] receptor on activated [[monocytes]].<ref name="Faulds-1994">{{Cite journal | last1 = Faulds | first1 = D. | last2 = Sorkin | first2 = EM. | title = Abciximab (c7E3 Fab). A review of its pharmacology and therapeutic potential in ischaemic heart disease. | journal = Drugs | volume = 48 | issue = 4 | pages = 583-98 | month = Oct | year = 1994 | doi = | PMID = 7528131 }}</ref> | Abciximab is a chimeric human-murine monoclonal antibody Fab fragment which inhibits [[platelet aggregation]] by binding to the glycoprotein IIb/IIIa receptors on platelets. It prevents [[fibrinogen]] and [[von Willebrand factor]] from binding to the receptor in a dose-dependent manner. Abciximab may also bind to the [[vitronectin]] receptor and to the [[Mac-1]] receptor on activated [[monocytes]].<ref name="Faulds-1994">{{Cite journal | last1 = Faulds | first1 = D. | last2 = Sorkin | first2 = EM. | title = Abciximab (c7E3 Fab). A review of its pharmacology and therapeutic potential in ischaemic heart disease. | journal = Drugs | volume = 48 | issue = 4 | pages = 583-98 | month = Oct | year = 1994 | doi = | PMID = 7528131 }}</ref> | ||
==References== | ==References== | ||
Revision as of 19:36, 29 January 2014
Template:Abciximab Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
For patient information, click here.
Overview
Abciximab (previously known as c7E3 Fab), a glycoprotein IIb/IIIa receptor antagonist manufactured by Janssen Biologics BV and distributed by Eli Lilly under the trade name ReoPro, is a platelet aggregation inhibitor mainly used during and after coronary artery procedures like angioplasty to prevent platelets from sticking together and causing thrombus (blood clot) formation within the coronary artery. It is a glycoprotein IIb/IIIa inhibitor.[1]
While abciximab has a short plasma half-life, due to its strong affinity for its receptor on the platelets, it may occupy some receptors for weeks. In practice, platelet aggregation gradually returns to normal about 96 to 120 hours after discontinuation of the drug.(Tanguay, J.F., Eur Heart J 1999; 1 (suppl E): E27-E35 Abciximab is made from the Fab fragments of an immunoglobulin that targets the glycoprotein IIb/IIIa receptor on the platelet membrane.[2]
Category
Antiplatelet, Glycoprotein IIb/IIIa Receptor Antagonist
US Brand Names
ReoPro®
FDA Package Insert
Indications and Usage | Dosage and Administration | Dosage Forms and Strengths | Contraindications | Warnings and Precautions | Adverse Reactions | Drug Interactions | Use in Specific Populations | Overdosage | Description | Clinical Pharmacology | Nonclinical Toxicology | Clinical Studies | How Supplied/Storage and Handling | Patient Counseling Information | Labels and Packages
Mechanism of Action
Abciximab is a chimeric human-murine monoclonal antibody Fab fragment which inhibits platelet aggregation by binding to the glycoprotein IIb/IIIa receptors on platelets. It prevents fibrinogen and von Willebrand factor from binding to the receptor in a dose-dependent manner. Abciximab may also bind to the vitronectin receptor and to the Mac-1 receptor on activated monocytes.[3]
References
- ↑ "Abciximab". Drugs.com. Archived from the original on 20 April 2010. Retrieved 13 March 2010.
- ↑ "International Nonproprietary Names for Pharmaceutiical Substances" (PDF). WHO Drug Information. 7 (4). 1993.
- ↑ Faulds, D.; Sorkin, EM. (1994). "Abciximab (c7E3 Fab). A review of its pharmacology and therapeutic potential in ischaemic heart disease". Drugs. 48 (4): 583–98. PMID 7528131. Unknown parameter
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