{"id":3822,"date":"2025-03-31T18:11:50","date_gmt":"2025-03-31T18:11:50","guid":{"rendered":"https:\/\/kidneydiseaseclinic.net\/kdc\/celecoxib-txt\/"},"modified":"2025-03-31T18:11:50","modified_gmt":"2025-03-31T18:11:50","slug":"celecoxib-txt","status":"publish","type":"post","link":"https:\/\/kidneydiseaseclinic.net\/kdc\/celecoxib-txt\/","title":{"rendered":"Celecoxib.txt"},"content":{"rendered":"<h1>Celecoxib<\/h1>\n<p><H3>  CLINICAL USE <\/H3><br \/>\nCox 2 inhibitor and analgesic<H3> DOSE IN NORMAL RENAL FUNCTION  <\/H3>200 mg once or twice daily<H3>  PHARMACOKINETICS    <\/H3><LI> Molecular weight &amp;nbsp  &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp  &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp :381.4<\/li>\n<li>  %Protein binding  &amp;nbsp &amp;nbsp &amp;nbsp  &amp;nbsp  &amp;nbsp  &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp :97<\/li>\n<li>  %Excreted unchanged in urine &amp;nbsp &amp;nbsp : &lt;3<\/li>\n<p><LI> Volume of distribution (L\/kg) &amp;nbsp &amp;nbsp &amp;nbsp :400 litres<\/li>\n<p><LI>half-life \u2013 normal\/ESRD (hrs)&amp;nbsp &amp;nbsp &amp;nbsp :8\u201312\/Unchanged<H3>  DOSE IN RENAL IMPAIRMENT <\/H3> <H4>GFR (mL\/MIN)<\/H4>30\u201350 Dose as in normal renal function. Use with caution10\u201330 Dose as in normal renal function, but avoid if possible<LI> &lt;10 &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp : Dose as in normal renal function, but only use if on dialysis<H3> DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES  <\/H3><LI> CAPD  &amp;nbsp &amp;nbsp &amp;nbsp  &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp:Unlikely to be dialysed. Dose as in normal renal function <\/p>\n<li> HD &amp;nbsp  &amp;nbsp &amp;nbsp  &amp;nbsp &amp;nbsp  &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp :Unlikely to be dialysed. Dose as in normal renal function <LI>HDF\/high flux  &amp;nbsp :Unknown dialysability. Dose as in normal renal function <LI>CAV\/VVHD  &amp;nbsp &amp;nbsp &amp;nbsp:Unknown dialysability. Dose as in GFR 10 to 20   mL\/min <H3> IMPORTANT DRUG INTERACTIONS  <\/H3>Potentially hazardous interactions with other drugs\n<li>ACE inhibitors and angiotensin-II  antagonists: antagonism of hypotensive effect; increased risk of nephrotoxicity and hyperkalaemia\n<li>Analgesics: avoid concomitant use of  2 or more NSAIDs, including aspirin (increased side effects); avoid with ketorolac (increased risk of side effects and haemorrhage)\n<li>Antibacterials: possibly increased risk of  convulsions with quinolones\n<li>Anticoagulants: effects of coumarins  enhanced; possibly increased risk of bleeding with heparins and coumarins\n<li>Antidepressants: increased risk of bleeding  with SSRIs and venlafaxine\n<li>Antidiabetic agents: effects of  sulphonylureas enhanced\n<li>Anti-epileptics: possibly increased  phenytoin concentration\n<li>Antifungals: if used with fluconazole, halve  the dose of celecoxib. Antivirals: increased risk of haematological  toxicity with zidovudine; concentration possibly increased by ritonavir\n<li>Ciclosporin: may potentiate nephrotoxicity Cytotoxic agents: reduced excretion of  methotrexate; increased risk of bleeding with erlotinib\n<li>Diuretics: increased risk of nephrotoxicity;  antagonism of diuretic effect; hyperkalaemia with potassium-sparing diuretics\n<li>Lithium: excretion decreased Pentoxifylline: possibly increased risk of  bleeding\n<li>Tacrolimus: increased risk of  nephrotoxicity<H3> ADMINISTRATION  <\/H3><H4> Reconstition<\/H4>\u2013<H4>  Route  <\/H4>Oral <H4>  Rate of Administration  <\/H4>\u2013<H4>Comments<\/H4>\u2013<H4>  OTHER INFORMATION  <\/H4>\n<li>Clinical trials have shown renal  effects similar to those observed with comparative NSAIDs.\n<li>Monitor patient for deterioration in renal function and fluid retention\n<li>Inhibition of renal prostaglandin synthesis  by NSAIDs may interfere with renal function, especially in the presence of existing renal disease.\n<li> Avoid if possible; if not, check serum creatinine 48\u201372 hours after starting NSAID.\n<li>If raised, discontinue NSAID therapy\n<li>Use normal doses in patients with ERF on  dialysis if they do not pass any urine. Use with caution in renal transplant  recipients \u2013 can reduce intrarenal autocoid synthesis\n<li>Celecoxib should be used with caution  in uraemic patients predisposed to gastrointestinal bleeding or uraemic coagulopathies\n<li>Contraindicated in patients with ischaemic  heart disease or cerebrovascular disease and class II\u2013IV NYHA congestive heart failure.<br \/>\n","protected":false},"excerpt":{"rendered":"<p>Celecoxib CLINICAL USE Cox 2 inhibitor and analgesic DOSE IN<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[7],"class_list":["post-3822","post","type-post","status-publish","format-standard","hentry","category-blog","tag-post-by-auto-php"],"_links":{"self":[{"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/posts\/3822","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/comments?post=3822"}],"version-history":[{"count":0,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/posts\/3822\/revisions"}],"wp:attachment":[{"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/media?parent=3822"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/categories?post=3822"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/tags?post=3822"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}