Difference between revisions of "Hydroxyurea (Hydrea)"

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*[[Essential thrombocythemia]]
 
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==Patient drug information==
 
==Patient drug information==
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[[Category:Essential thrombocythemia medications]]
 
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[[Category:Drugs FDA approved in 1967]]
 
[[Category:Drugs FDA approved in 1967]]

Revision as of 01:42, 21 February 2015

General information

Class/mechanism: Exact mechanism unclear, but data suggests that hydroxyurea inhibits DNA synthesis by inhibiting ribonucleotide reductase, which inhibits cancer cell growth. May sensitize tumors to radiation by keeping cells in the G1 phase of the cell cycle, where they are most vulnerable to radiation, and/or by interfering with DNA repair processes. Does not appear to affect RNA and protein synthesis.[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, UpToDate (courtesy of Lexicomp), or the prescribing information.[1]

Diseases for which it is used

Patient drug information

History of changes in FDA indication

  • 12/7/1967: Initial FDA approval

Also known as

Synonyms
APO-Hydroxyurea Biosupressin Cytodrox Dhnp Droxia
Droxiurea Durea GEN-Hydroxyurea Hidrea Hidroxiurea Delta Farma
Hidroxiurea Martian Hidroxiurea Microsules Hondrea Hydab Hydrea
Hydrine Hydrourea Hydroxycarbam Hydroxycarbamid Hydroxycarbamide
Hydroxyurea Hydroxyurea Medac Hytas Litalir Myelostat
Mylocel Neodrea Onco Carbide Syrea Ureax

References