Palonosetron: Difference between revisions
Rabin Bista (talk | contribs) No edit summary |
Rabin Bista (talk | contribs) No edit summary |
||
Line 4: | Line 4: | ||
| verifiedrevid = 464197120 | | verifiedrevid = 464197120 | ||
| IUPAC_name = (3''aS'')-2-[(3''S'')-1-Azabicyclo[2.2.2]oct-3-yl]-2,3,3''a'',4,5,6-hexahydro-1''H''-benz[''de'']isoquinolin-1-one | | IUPAC_name = (3''aS'')-2-[(3''S'')-1-Azabicyclo[2.2.2]oct-3-yl]-2,3,3''a'',4,5,6-hexahydro-1''H''-benz[''de'']isoquinolin-1-one | ||
| image = Palonosetron | | image = Palonosetron Wiki Str.png | ||
| width = 200 | | width = 200 | ||
Line 54: | Line 54: | ||
| StdInChIKey = CPZBLNMUGSZIPR-NVXWUHKLSA-N | | StdInChIKey = CPZBLNMUGSZIPR-NVXWUHKLSA-N | ||
}} | }} | ||
__NOTOC__ | |||
{{SI}} | |||
{{CMG}} | |||
== Overview == | |||
'''Palonosetron''' ([[International Nonproprietary Name|INN]], trade name '''Aloxi''') is a [[5-HT3 antagonist|5-HT<sub>3</sub> antagonist]] used in the prevention and treatment of [[chemotherapy-induced nausea and vomiting]] (CINV). It is used for the control of delayed CINV—nausea and vomiting and there are tentative data to suggest that it may be better than [[granisetron]].<ref>{{cite journal|last=Billio|first=A|author2=Morello, E |author3=Clarke, MJ |title=Serotonin receptor antagonists for highly emetogenic chemotherapy in adults.|journal=The Cochrane database of systematic reviews|date=Jan 20, 2010|issue=1|pages=CD006272|pmid=20091591|doi=10.1002/14651858.CD006272.pub2}}</ref> | '''Palonosetron''' ([[International Nonproprietary Name|INN]], trade name '''Aloxi''') is a [[5-HT3 antagonist|5-HT<sub>3</sub> antagonist]] used in the prevention and treatment of [[chemotherapy-induced nausea and vomiting]] (CINV). It is used for the control of delayed CINV—nausea and vomiting and there are tentative data to suggest that it may be better than [[granisetron]].<ref>{{cite journal|last=Billio|first=A|author2=Morello, E |author3=Clarke, MJ |title=Serotonin receptor antagonists for highly emetogenic chemotherapy in adults.|journal=The Cochrane database of systematic reviews|date=Jan 20, 2010|issue=1|pages=CD006272|pmid=20091591|doi=10.1002/14651858.CD006272.pub2}}</ref> | ||
Line 62: | Line 65: | ||
==References== | ==References== | ||
{{Reflist}} | {{Reflist|2}} | ||
{{5-HT3 antagonists}} | {{5-HT3 antagonists}} | ||
{{Serotonergics}} | {{Serotonergics}} | ||
[[Category:Drug]] | |||
[[Category:5-HT3 antagonists]] | [[Category:5-HT3 antagonists]] | ||
[[Category:Quinuclidines]] | [[Category:Quinuclidines]] |
Latest revision as of 13:54, 9 April 2015
Clinical data | |
---|---|
AHFS/Drugs.com | Monograph |
MedlinePlus | a610002 |
[[Regulation of therapeutic goods |Template:Engvar data]] |
|
Pregnancy category | |
Routes of administration | Intravenous, oral |
ATC code | |
Legal status | |
Legal status |
|
Pharmacokinetic data | |
Bioavailability | 97% (oral) |
Protein binding | 62% |
Metabolism | Hepatic, 50% (mostly CYP2D6-mediated, CYP3A4 and CYP1A2 also involved) |
Elimination half-life | Approximately 40 hours |
Excretion | Renal, 80% (of which 49% unchanged); fecal (5 to 8%) |
Identifiers | |
| |
CAS Number | |
PubChem CID | |
DrugBank | |
ChemSpider | |
UNII | |
ChEBI | |
ChEMBL | |
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 | C19H24N2O |
Molar mass | 296.407 g/mol |
3D model (JSmol) | |
| |
| |
(what is this?) (verify) |
WikiDoc Resources for Palonosetron |
Articles |
---|
Most recent articles on Palonosetron Most cited articles on Palonosetron |
Media |
Powerpoint slides on Palonosetron |
Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Palonosetron at Clinical Trials.gov Clinical Trials on Palonosetron at Google
|
Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Palonosetron
|
Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Patient resources on Palonosetron Discussion groups on Palonosetron Patient Handouts on Palonosetron Directions to Hospitals Treating Palonosetron Risk calculators and risk factors for Palonosetron
|
Healthcare Provider Resources |
Causes & Risk Factors for Palonosetron |
Continuing Medical Education (CME) |
International |
|
Business |
Experimental / Informatics |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Palonosetron (INN, trade name Aloxi) is a 5-HT3 antagonist used in the prevention and treatment of chemotherapy-induced nausea and vomiting (CINV). It is used for the control of delayed CINV—nausea and vomiting and there are tentative data to suggest that it may be better than granisetron.[1]
Palonosetron is administered intravenously, as a single dose, 30 minutes before chemotherapy,[2] or as a single oral capsule one hour before chemotherapy.[3] The oral formulation was approved on August 22, 2008 for prevention of acute CINV alone, as a large clinical trial did not show oral administration to be as effective as intravenous use against delayed CINV.[3]
See also
References
- ↑ Billio, A; Morello, E; Clarke, MJ (Jan 20, 2010). "Serotonin receptor antagonists for highly emetogenic chemotherapy in adults". The Cochrane database of systematic reviews (1): CD006272. doi:10.1002/14651858.CD006272.pub2. PMID 20091591.
- ↑ De Leon A (2006). "Palonosetron (Aloxi): a second-generation 5-HT(3) receptor antagonist for chemotherapy-induced nausea and vomiting". Proceedings (Baylor University. Medical Center). 19 (4): 413–6. PMC 1618755. PMID 17106506.
- ↑ 3.0 3.1 Waknine, Yael (September 4, 2008). "FDA Approvals: Nplate, Aloxi, Vidaza". Medscape. Retrieved 2008-09-04. Freely available with registration.
- Pages with script errors
- Template:drugs.com link with non-standard subpage
- Articles with changed CASNo identifier
- Articles with changed EBI identifier
- E number from Wikidata
- ECHA InfoCard ID from Wikidata
- Chemical articles with unknown parameter in Infobox drug
- Articles without KEGG source
- Drugboxes which contain changes to verified fields
- Drugboxes which contain changes to watched fields
- Drug
- 5-HT3 antagonists
- Quinuclidines
- Isoquinolines
- Lactams