Difference between revisions of "Bicalutamide (Casodex)"

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*[http://chemocare.com/chemotherapy/drug-info/bicalutamide.aspx Bicalutamide (Casodex) patient drug information (Chemocare)]<ref>[http://chemocare.com/chemotherapy/drug-info/bicalutamide.aspx Bicalutamide (Casodex) patient drug information (Chemocare)]</ref>
 
*[http://chemocare.com/chemotherapy/drug-info/bicalutamide.aspx Bicalutamide (Casodex) patient drug information (Chemocare)]<ref>[http://chemocare.com/chemotherapy/drug-info/bicalutamide.aspx Bicalutamide (Casodex) patient drug information (Chemocare)]</ref>
 
*[http://www.uptodate.com/contents/bicalutamide-patient-drug-information Bicalutamide (Casodex) patient drug information (UpToDate)]<ref>[http://www.uptodate.com/contents/bicalutamide-patient-drug-information Bicalutamide (Casodex) patient drug information (UpToDate)]</ref>
 
*[http://www.uptodate.com/contents/bicalutamide-patient-drug-information Bicalutamide (Casodex) patient drug information (UpToDate)]<ref>[http://www.uptodate.com/contents/bicalutamide-patient-drug-information Bicalutamide (Casodex) patient drug information (UpToDate)]</ref>
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==History of changes in FDA indication==
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*10/4/1995: Initial FDA approval
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*5/11/2005: Indicated for use in combination therapy with a luteinizing hormone-releasing hormone (LHRH) analogue for the treatment of Stage D2 metastatic [[Prostate cancer | carcinoma of the prostate]].
  
 
==References==
 
==References==
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[[Category:Androgen receptor inhibitors]]
 
[[Category:Androgen receptor inhibitors]]
 
[[Category:Prostate cancer medications]]
 
[[Category:Prostate cancer medications]]
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[[Category:Drugs FDA approved in 1995]]

Revision as of 21:20, 7 October 2014

Also known as Cosudex, Calutide, or Kalumid.

General information

Class/mechanism: Antiandrogen; non-steroidal androgen receptor inhibitor that competitively inhibits androgens by binding to cytosol androgen receptors.[1][2]
Route: PO
Extravasation: n/a

For conciseness and simplicity, HemOnc.org currently will focus on treatment regimens and not list information such as: renal/hepatic dose adjustments, metabolism (including CYP450), excretion, monitoring parameters (although this will be considered for checklists), or manufacturer. Instead, for the most current information, please refer to your preferred pharmacopeias such as Micromedex, Lexicomp, MedscapeUpToDate (courtesy of Lexicomp), or the prescribing information.[1]

Diseases for which it is used

Patient drug information

History of changes in FDA indication

  • 10/4/1995: Initial FDA approval
  • 5/11/2005: Indicated for use in combination therapy with a luteinizing hormone-releasing hormone (LHRH) analogue for the treatment of Stage D2 metastatic carcinoma of the prostate.

References