Difference between revisions of "Thalidomide (Thalomid)"

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==Patient drug information==
 
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[[Category:Immunomodulatory drugs (IMiDs)]]
 
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[[Category:Multiple myeloma medications]]
 
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[[Category:Drugs FDA approved in 1998]]
 
[[Category:Drugs FDA approved in 1998]]

Revision as of 02:49, 20 November 2014

General information

Class/mechanism: Immunomodulatory drug (IMiD); mechanism not fully understood.

Thalidomide's mechanism may involve immunomodulatory, antiinflammatory, and antiangiogenic effects and suppression of tumor necrosis factor-alpha (TNF-α) from peripheral blood mononuclear cells. Thalidomide has been observed to inhibit angiogenesis in a human umbilical artery explant model in vitro.[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

  • Note: thalidomide was introduced in 1957 but never FDA approved during that time period. It was taken off the global market in November 1961 due to birth defects, and was not FDA approved until 1998, at that time for a non-cancer indication (erythema nodosum leprosum).
  • 5/25/2006: First cancer-specific FDA indication: "in combination with dexamethasone is indicated for the treatment of patients with newly diagnosed multiple myeloma."

References