Argatroban: Difference between revisions
m Changed protection level for "Argatroban" ([Edit=Allow only autoconfirmed users] (expires 02:57, 14 March 2014 (UTC)) [Move=Allow only autoconfirmed users] (expires 02:57, 14 March 2014 (UTC))) |
No edit summary |
||
Line 19: | Line 19: | ||
}} | }} | ||
{{SI}} | {{SI}} | ||
{{CMG}} | {{CMG}}{{JH}} | ||
Line 28: | Line 28: | ||
It is manufactured by [[GlaxoSmithKline]]. | It is manufactured by [[GlaxoSmithKline]]. | ||
==Category== | |||
ADP receptor inhibitors;Triazolopyrimidines;Organofluorides;Alcohols;AstraZeneca | |||
==FDA Package Insert== | |||
====BRILINTA (ticagrelor) tablet ==== | |||
''' [[Ticagrelor indications and usage|Indications and Usage]]''' | |||
'''| [[Ticagrelor dosage and administration|Dosage and Administration]]''' | |||
'''| [[Ticagrelor dosage forms and strengths|Dosage Forms and Strengths]]''' | |||
'''| [[Ticagrelor contraindications|Contraindications]]''' | |||
'''| [[Ticagrelor warnings and precautions|Warnings and Precautions]]''' | |||
'''| [[Ticagrelor adverse reactions|Adverse Reactions]]''' | |||
'''| [[Ticagrelor drug interactions|Drug Interactions]]''' | |||
'''| [[Ticagrelor use in specific populations|Use in Specific Populations]]''' | |||
'''| [[Ticagrelor overdosage|Overdosage]]''' | |||
'''| [[Ticagrelor description|Description]]''' | |||
'''| [[Ticagrelor clinical pharmacology|Clinical Pharmacology]]''' | |||
'''| [[Ticagrelor nonclinical toxicology|Nonclinical Toxicology]]''' | |||
'''| [[Ticagrelor clinical studies|Clinical Studies]]''' | |||
'''| [[Ticagrelor how supplied storage and handling|How Supplied/Storage and Handling]]''' | |||
'''| [[Ticagrelor patient counseling information|Patient Counseling Information]]''' | |||
'''| [[Ticagrelor labels and packages|Labels and Packages]]''' | |||
==Reference== | ==Reference== |
Revision as of 22:42, 3 March 2014
Clinical data | |
---|---|
Routes of administration | intravenous |
ATC code | |
Pharmacokinetic data | |
Bioavailability | 100% (intravenous) |
Protein binding | 54% |
Metabolism | hepatic |
Elimination half-life | 39 and 51 minutes |
Identifiers | |
| |
CAS Number | |
PubChem CID | |
DrugBank | |
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 | C23H36N6O5S |
Molar mass | 508.635 g/mol |
WikiDoc Resources for Argatroban |
Articles |
---|
Most recent articles on Argatroban |
Media |
Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Argatroban at Clinical Trials.gov Clinical Trials on Argatroban at Google
|
Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Argatroban
|
Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Patient resources on Argatroban Discussion groups on Argatroban Patient Handouts on Argatroban Directions to Hospitals Treating Argatroban Risk calculators and risk factors for Argatroban
|
Healthcare Provider Resources |
Causes & Risk Factors for Argatroban |
Continuing Medical Education (CME) |
International |
|
Business |
Experimental / Informatics |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Jesus Rosario Hernandez, M.D. [2]
Argatroban is an anticoagulant that is a small molecule direct thrombin inhibitor. In 2000, argatroban was licensed by the Food and Drug Administration (FDA) for prophylaxis or treatment of thrombosis in patients with heparin-induced thrombocytopenia. In 2002, it was approved for use during percutaneous coronary interventions in patients who have or at risk for developing HIT.
Argatroban is given intravenously. Argatroban is metabolized in the liver and has a half life of about 50 minutes. It is monitored by PTT. Because of its hepatic metabolism, it may be used in patients with renal dysfunction. (This is in contrast to lepirudin, a direct thrombin inhibitor that is primarily renally cleared).
It is manufactured by GlaxoSmithKline.
Category
ADP receptor inhibitors;Triazolopyrimidines;Organofluorides;Alcohols;AstraZeneca
FDA Package Insert
BRILINTA (ticagrelor) tablet
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
Reference
- Di Nisio M, Middeldorp S, Buller HR. Direct thrombin inhibitors. N Engl J Med 2005;353:1028-40. PMID 16148288.
External links
- Pages with script errors
- E number from Wikidata
- ECHA InfoCard ID from Wikidata
- Articles without EBI source
- Chemical pages without ChemSpiderID
- Articles without KEGG source
- Articles without InChI source
- Articles without UNII source
- Drugs with no legal status
- Articles containing unverified chemical infoboxes
- Hematology
- Anticoagulants
- Drugs