Pharmacokinetics of Etoricoxib in Patients with Renal Impairment
The effect of renal insufficiency on the pharmacokinetics of etoricoxib, a selective inhibitor of cyclooxygenase‐2, was examined in 23 patients with varying degrees of renal impairment (12 moderate [creatinine clearance between 30 and 50 mL/min/1.73 m2], 5 severe [creatinine clearance below 30 mL/mi...
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Veröffentlicht in: | Journal of clinical pharmacology 2004-01, Vol.44 (1), p.48-58 |
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creator | Agrawal, Nancy G. B. Matthews, Catherine Z. Mazenko, Ralph S. Kline, Walter F. Woolf, Eric J. Porras, Arturo G. Geer, Leslie A. Wong, Peggy H. Cho, Meehung Cote, Josee Marbury, Thomas C. Moncrief, Jack W. Alcorn Jr, Harry Swan, Suzanne Sack, Marshall R. Robson, Richard A. Petty, Kevin J. Schwartz, Jules I. Gottesdiener, Keith M. |
description | The effect of renal insufficiency on the pharmacokinetics of etoricoxib, a selective inhibitor of cyclooxygenase‐2, was examined in 23 patients with varying degrees of renal impairment (12 moderate [creatinine clearance between 30 and 50 mL/min/1.73 m2], 5 severe [creatinine clearance below 30 mL/min/1.73 m2], and 6 with end‐stage renal disease requiring hemodialysis) following administration of single 120‐mg oral doses of etoricoxib. Even the most severe renal impairment was found to have little effect on etoricoxib pharmacokinetics. The low recovery of etoricoxib in dialysate (less than 6% of the dose) supports that hemodialysis also has little effect on etoricoxib pharmacokinetics, and binding of etoricoxib to plasma proteins was generally unaffected by renal disease. Single doses of etoricoxib were generally well tolerated by patients with renal impairment. Based on pharmacokinetic considerations, dosing adjustments are not necessary for patients with any degree of renal impairment. However, because patients with advanced renal disease (creatinine clearance below 30 mL/min/1.73 m2) are likely to be very sensitive to any further compromise of renal function, and there is no long‐term clinical experience in these patients, the use of etoricoxib is not recommended in patients with advanced renal disease. |
doi_str_mv | 10.1177/0091270003260338 |
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B. ; Matthews, Catherine Z. ; Mazenko, Ralph S. ; Kline, Walter F. ; Woolf, Eric J. ; Porras, Arturo G. ; Geer, Leslie A. ; Wong, Peggy H. ; Cho, Meehung ; Cote, Josee ; Marbury, Thomas C. ; Moncrief, Jack W. ; Alcorn Jr, Harry ; Swan, Suzanne ; Sack, Marshall R. ; Robson, Richard A. ; Petty, Kevin J. ; Schwartz, Jules I. ; Gottesdiener, Keith M.</creator><creatorcontrib>Agrawal, Nancy G. B. ; Matthews, Catherine Z. ; Mazenko, Ralph S. ; Kline, Walter F. ; Woolf, Eric J. ; Porras, Arturo G. ; Geer, Leslie A. ; Wong, Peggy H. ; Cho, Meehung ; Cote, Josee ; Marbury, Thomas C. ; Moncrief, Jack W. ; Alcorn Jr, Harry ; Swan, Suzanne ; Sack, Marshall R. ; Robson, Richard A. ; Petty, Kevin J. ; Schwartz, Jules I. ; Gottesdiener, Keith M.</creatorcontrib><description>The effect of renal insufficiency on the pharmacokinetics of etoricoxib, a selective inhibitor of cyclooxygenase‐2, was examined in 23 patients with varying degrees of renal impairment (12 moderate [creatinine clearance between 30 and 50 mL/min/1.73 m2], 5 severe [creatinine clearance below 30 mL/min/1.73 m2], and 6 with end‐stage renal disease requiring hemodialysis) following administration of single 120‐mg oral doses of etoricoxib. Even the most severe renal impairment was found to have little effect on etoricoxib pharmacokinetics. The low recovery of etoricoxib in dialysate (less than 6% of the dose) supports that hemodialysis also has little effect on etoricoxib pharmacokinetics, and binding of etoricoxib to plasma proteins was generally unaffected by renal disease. Single doses of etoricoxib were generally well tolerated by patients with renal impairment. Based on pharmacokinetic considerations, dosing adjustments are not necessary for patients with any degree of renal impairment. However, because patients with advanced renal disease (creatinine clearance below 30 mL/min/1.73 m2) are likely to be very sensitive to any further compromise of renal function, and there is no long‐term clinical experience in these patients, the use of etoricoxib is not recommended in patients with advanced renal disease.</description><identifier>ISSN: 0091-2700</identifier><identifier>EISSN: 1552-4604</identifier><identifier>DOI: 10.1177/0091270003260338</identifier><identifier>PMID: 14681341</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Administration, Oral ; Adult ; Aged ; Area Under Curve ; bioavailability ; Biological Availability ; Clinical Trials as Topic ; COX-2 ; cyclooxygenase ; Cyclooxygenase Inhibitors - pharmacokinetics ; Etoricoxib ; Female ; Half-Life ; Humans ; Kidney Failure, Chronic - metabolism ; Kidney Failure, Chronic - therapy ; Male ; Metabolic Clearance Rate ; Middle Aged ; pharmacokinetics ; Protein Binding ; Pyridines - pharmacokinetics ; Renal Dialysis ; renal impairment ; Sulfones - pharmacokinetics</subject><ispartof>Journal of clinical pharmacology, 2004-01, Vol.44 (1), p.48-58</ispartof><rights>2004 American College of Clinical Pharmacology</rights><rights>2004 SAGE Publications</rights><rights>Copyright SAGE PUBLICATIONS, INC. Jan 2004</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4795-6c369407ecc110900797035007fd7d062995bfe755d6ba327d02cc97be3649553</citedby><cites>FETCH-LOGICAL-c4795-6c369407ecc110900797035007fd7d062995bfe755d6ba327d02cc97be3649553</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1177%2F0091270003260338$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1177%2F0091270003260338$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27929,27930,45579,45580</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14681341$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Agrawal, Nancy G. B.</creatorcontrib><creatorcontrib>Matthews, Catherine Z.</creatorcontrib><creatorcontrib>Mazenko, Ralph S.</creatorcontrib><creatorcontrib>Kline, Walter F.</creatorcontrib><creatorcontrib>Woolf, Eric J.</creatorcontrib><creatorcontrib>Porras, Arturo G.</creatorcontrib><creatorcontrib>Geer, Leslie A.</creatorcontrib><creatorcontrib>Wong, Peggy H.</creatorcontrib><creatorcontrib>Cho, Meehung</creatorcontrib><creatorcontrib>Cote, Josee</creatorcontrib><creatorcontrib>Marbury, Thomas C.</creatorcontrib><creatorcontrib>Moncrief, Jack W.</creatorcontrib><creatorcontrib>Alcorn Jr, Harry</creatorcontrib><creatorcontrib>Swan, Suzanne</creatorcontrib><creatorcontrib>Sack, Marshall R.</creatorcontrib><creatorcontrib>Robson, Richard A.</creatorcontrib><creatorcontrib>Petty, Kevin J.</creatorcontrib><creatorcontrib>Schwartz, Jules I.</creatorcontrib><creatorcontrib>Gottesdiener, Keith M.</creatorcontrib><title>Pharmacokinetics of Etoricoxib in Patients with Renal Impairment</title><title>Journal of clinical pharmacology</title><addtitle>J Clin Pharmacol</addtitle><description>The effect of renal insufficiency on the pharmacokinetics of etoricoxib, a selective inhibitor of cyclooxygenase‐2, was examined in 23 patients with varying degrees of renal impairment (12 moderate [creatinine clearance between 30 and 50 mL/min/1.73 m2], 5 severe [creatinine clearance below 30 mL/min/1.73 m2], and 6 with end‐stage renal disease requiring hemodialysis) following administration of single 120‐mg oral doses of etoricoxib. Even the most severe renal impairment was found to have little effect on etoricoxib pharmacokinetics. The low recovery of etoricoxib in dialysate (less than 6% of the dose) supports that hemodialysis also has little effect on etoricoxib pharmacokinetics, and binding of etoricoxib to plasma proteins was generally unaffected by renal disease. Single doses of etoricoxib were generally well tolerated by patients with renal impairment. Based on pharmacokinetic considerations, dosing adjustments are not necessary for patients with any degree of renal impairment. However, because patients with advanced renal disease (creatinine clearance below 30 mL/min/1.73 m2) are likely to be very sensitive to any further compromise of renal function, and there is no long‐term clinical experience in these patients, the use of etoricoxib is not recommended in patients with advanced renal disease.</description><subject>Administration, Oral</subject><subject>Adult</subject><subject>Aged</subject><subject>Area Under Curve</subject><subject>bioavailability</subject><subject>Biological Availability</subject><subject>Clinical Trials as Topic</subject><subject>COX-2</subject><subject>cyclooxygenase</subject><subject>Cyclooxygenase Inhibitors - pharmacokinetics</subject><subject>Etoricoxib</subject><subject>Female</subject><subject>Half-Life</subject><subject>Humans</subject><subject>Kidney Failure, Chronic - metabolism</subject><subject>Kidney Failure, Chronic - therapy</subject><subject>Male</subject><subject>Metabolic Clearance Rate</subject><subject>Middle Aged</subject><subject>pharmacokinetics</subject><subject>Protein Binding</subject><subject>Pyridines - pharmacokinetics</subject><subject>Renal Dialysis</subject><subject>renal impairment</subject><subject>Sulfones - pharmacokinetics</subject><issn>0091-2700</issn><issn>1552-4604</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1vEzEQxS1ERUPhzgmtOHDbdvwd30BRaUsrCKjA0fI6XsXN7jrYXqX97-tVIir1wunJM7_3NH4IvcNwirGUZwAKEwkAlAigdP4CzTDnpGYC2Es0m9b1tD9Gr1O6A8CCcfwKHWMm5pgyPEOflmsTe2PDxg8ue5uq0FbnOURvw71vKj9US5O9G3Kqdj6vq59uMF111W-Nj30Zv0FHremSe3vQE_Try_nt4rK--X5xtfh8U1smFa-FpUIxkM5ajEEBSCWB8qLtSq5AEKV40zrJ-Uo0hpIyI9Yq2TgqmOKcnqCP-9xtDH9Hl7LufbKu68zgwpi0xFxwwkkBPzwD78IYy9FJE8rnSigqCgR7yMaQUnSt3kbfm_igMeipWv282mJ5f8gdm96tngyHLgvA9sAudNnFtOnGnYt67UyX1yUPgJW8mhQFXF71NJo-xg8237mH_96hvy6Wl0rQ4qv3Pp-yu__nM3GjhaSS6z_fLrT88ZvcXs-ZFvQRlkueVw</recordid><startdate>200401</startdate><enddate>200401</enddate><creator>Agrawal, Nancy G. 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B.</au><au>Matthews, Catherine Z.</au><au>Mazenko, Ralph S.</au><au>Kline, Walter F.</au><au>Woolf, Eric J.</au><au>Porras, Arturo G.</au><au>Geer, Leslie A.</au><au>Wong, Peggy H.</au><au>Cho, Meehung</au><au>Cote, Josee</au><au>Marbury, Thomas C.</au><au>Moncrief, Jack W.</au><au>Alcorn Jr, Harry</au><au>Swan, Suzanne</au><au>Sack, Marshall R.</au><au>Robson, Richard A.</au><au>Petty, Kevin J.</au><au>Schwartz, Jules I.</au><au>Gottesdiener, Keith M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pharmacokinetics of Etoricoxib in Patients with Renal Impairment</atitle><jtitle>Journal of clinical pharmacology</jtitle><addtitle>J Clin Pharmacol</addtitle><date>2004-01</date><risdate>2004</risdate><volume>44</volume><issue>1</issue><spage>48</spage><epage>58</epage><pages>48-58</pages><issn>0091-2700</issn><eissn>1552-4604</eissn><abstract>The effect of renal insufficiency on the pharmacokinetics of etoricoxib, a selective inhibitor of cyclooxygenase‐2, was examined in 23 patients with varying degrees of renal impairment (12 moderate [creatinine clearance between 30 and 50 mL/min/1.73 m2], 5 severe [creatinine clearance below 30 mL/min/1.73 m2], and 6 with end‐stage renal disease requiring hemodialysis) following administration of single 120‐mg oral doses of etoricoxib. Even the most severe renal impairment was found to have little effect on etoricoxib pharmacokinetics. The low recovery of etoricoxib in dialysate (less than 6% of the dose) supports that hemodialysis also has little effect on etoricoxib pharmacokinetics, and binding of etoricoxib to plasma proteins was generally unaffected by renal disease. Single doses of etoricoxib were generally well tolerated by patients with renal impairment. Based on pharmacokinetic considerations, dosing adjustments are not necessary for patients with any degree of renal impairment. However, because patients with advanced renal disease (creatinine clearance below 30 mL/min/1.73 m2) are likely to be very sensitive to any further compromise of renal function, and there is no long‐term clinical experience in these patients, the use of etoricoxib is not recommended in patients with advanced renal disease.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>14681341</pmid><doi>10.1177/0091270003260338</doi><tpages>11</tpages></addata></record> |
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subjects | Administration, Oral Adult Aged Area Under Curve bioavailability Biological Availability Clinical Trials as Topic COX-2 cyclooxygenase Cyclooxygenase Inhibitors - pharmacokinetics Etoricoxib Female Half-Life Humans Kidney Failure, Chronic - metabolism Kidney Failure, Chronic - therapy Male Metabolic Clearance Rate Middle Aged pharmacokinetics Protein Binding Pyridines - pharmacokinetics Renal Dialysis renal impairment Sulfones - pharmacokinetics |
title | Pharmacokinetics of Etoricoxib in Patients with Renal Impairment |
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