Difference between revisions of "Dutasteride (Avodart)"

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==General information==
 
==General information==
Class/mechanism: 5 alpha-reductase inhibitor; inhibits conversion of testosterone to dihydrotestosterone (DHT).  Competitively inhibits type 1 and 2 5 alpha-reductase isoenzymes by forming a stable enzyme complex with them.<ref name="insert">[http://us.gsk.com/products/assets/us_avodart.pdf Dutasteride (Avodart) package insert]</ref><ref>[[Media:Dutasteride.pdf | Dutasteride (Avodart) package insert (locally hosted backup)]]</ref><ref>[http://www.avodart.com Avodart manufacturer's website]</ref>
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Class/mechanism: 5 alpha-reductase inhibitor; inhibits conversion of testosterone to dihydrotestosterone (DHT).  Competitively inhibits type 1 and 2 5 alpha-reductase isoenzymes by forming a stable enzyme complex with them.<ref name="insert">[https://www.accessdata.fda.gov/drugsatfda_docs/label/2008/021319s014lbl.pdf Dutasteride (Avodart) package insert]</ref><ref>[[Media:Dutasteride.pdf | Dutasteride (Avodart) package insert (locally hosted backup)]]</ref><ref>[http://www.avodart.com Avodart manufacturer's website]</ref>
 
<br>Route: PO
 
<br>Route: PO
 
<br>Extravasation: n/a
 
<br>Extravasation: n/a
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==Patient drug information==
 
==Patient drug information==
*[http://us.gsk.com/products/assets/us_avodart.pdf#page=26 Dutasteride (Avodart) package insert pages 26-29]<ref name="insert"></ref>  
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*[https://www.accessdata.fda.gov/drugsatfda_docs/label/2008/021319s014lbl.pdf#page=26 Dutasteride (Avodart) package insert pages 26-29]<ref name="insert"></ref>  
 
*[http://www.uptodate.com/contents/dutasteride-patient-drug-information Dutasteride (Avodart) patient drug information (UpToDate)]<ref>[http://www.uptodate.com/contents/dutasteride-patient-drug-information Dutasteride (Avodart) patient drug information (UpToDate)]</ref>
 
*[http://www.uptodate.com/contents/dutasteride-patient-drug-information Dutasteride (Avodart) patient drug information (UpToDate)]<ref>[http://www.uptodate.com/contents/dutasteride-patient-drug-information Dutasteride (Avodart) patient drug information (UpToDate)]</ref>
  

Revision as of 10:49, 4 April 2021

General information

Class/mechanism: 5 alpha-reductase inhibitor; inhibits conversion of testosterone to dihydrotestosterone (DHT). Competitively inhibits type 1 and 2 5 alpha-reductase isoenzymes by forming a stable enzyme complex with them.[1][2][3]
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, UpToDate (courtesy of Lexicomp), or the prescribing information.[1]

Diseases for which it is used

Patient drug information

History of changes in FDA indication

  • 11/20/2001: Initial FDA approval "for the treatment of symptomatic benign prostatic hyperplasia (BPH) in men with an enlarged prostate gland."
  • 6/9/2011: New FDA Limitation of Use: "AVODART is not approved for the prevention of prostate cancer."

Also known as

  • Brand name: Avodart

References