Difference between revisions of "Histrelin (Vantas)"

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(Created page with "=Mechanism of action= Histrelin acetate, an LH-RH agonist, acts as a potent inhibitor of gonadotropin secretion when given continuously in therapeutic doses. Both animal and h...")
 
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=Mechanism of action=
 
=Mechanism of action=
Histrelin acetate, an LH-RH agonist, acts as a potent inhibitor of gonadotropin secretion when given continuously in therapeutic doses. Both animal and human studies indicate that following an initial stimulatory phase, chronic, subcutaneous administration of histrelin acetate desensitizes responsiveness of the pituitary gonadotropin which, in turn, causes a reduction in testicular steroidogenesis.
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Histrelin acetate, an LH-RH agonist, acts as a potent inhibitor of gonadotropin secretion when given continuously in therapeutic doses. Both animal and human studies indicate that following an initial stimulatory phase, chronic, subcutaneous administration of histrelin acetate desensitizes responsiveness of the pituitary gonadotropin which, in turn, causes a reduction in testicular steroidogenesis.<ref name="insert">[http://www.endo.com/File%20Library/Products/Prescribing%20Information/VANTAS.pdf Histrelin (Vantas) package insert]</ref><ref>[[Media:Histrelin.pdf | Histrelin (Vantas) package insert (locally hosted backup)]]</ref><ref>[http://www.vantasimplant.com/ Vantas implant manufacturer's website]</ref>
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<br>Route: subcutaneous
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<br>Extravasation: no information
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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 [http://www.thomsonhc.com/home/dispatch Micromedex], [http://online.lexi.com/ Lexicomp], [http://www.utdol.com/online/content/search.do UpToDate (courtesy of Lexicomp)], or the prescribing information.<ref name="insert"></ref>
  
 
=Diseases for which it is used=
 
=Diseases for which it is used=
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=History of changes in FDA indication=
 
=History of changes in FDA indication=
 
*10/12/2004: Initial FDA approval "in the palliative treatment of advanced [[prostate cancer]]."
 
*10/12/2004: Initial FDA approval "in the palliative treatment of advanced [[prostate cancer]]."
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==Patient drug information==
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*[http://www.endo.com/File%20Library/Products/Prescribing%20Information/VANTAS.pdf Histrelin (Vantas) package insert]<ref name="insert"></ref>
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==References==
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<references/>
  
 
[[Category:Drug index]]
 
[[Category:Drug index]]

Revision as of 01:43, 19 March 2017

Mechanism of action

Histrelin acetate, an LH-RH agonist, acts as a potent inhibitor of gonadotropin secretion when given continuously in therapeutic doses. Both animal and human studies indicate that following an initial stimulatory phase, chronic, subcutaneous administration of histrelin acetate desensitizes responsiveness of the pituitary gonadotropin which, in turn, causes a reduction in testicular steroidogenesis.[1][2][3]
Route: subcutaneous
Extravasation: no information

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

History of changes in FDA indication

  • 10/12/2004: Initial FDA approval "in the palliative treatment of advanced prostate cancer."

Patient drug information

References