{"id":4532,"date":"2025-03-31T18:12:11","date_gmt":"2025-03-31T18:12:11","guid":{"rendered":"https:\/\/kidneydiseaseclinic.net\/kdc\/indometacin-txt\/"},"modified":"2025-03-31T18:12:11","modified_gmt":"2025-03-31T18:12:11","slug":"indometacin-txt","status":"publish","type":"post","link":"https:\/\/kidneydiseaseclinic.net\/kdc\/indometacin-txt\/","title":{"rendered":"indometacin.txt"},"content":{"rendered":"<h1>  indometacin  <\/h1>\n<p><H3>  CLINICAL USE <\/H3><br \/>\nNSAID:Pain and inflammation in rheumatic  disease and other musculoskeletal disordersAcute gout Dysmenorrhoea Closure of ductus arteriosus <H3> DOSE IN NORMAL RENAL FUNCTION  <\/H3>Oral: 50\u2013200 mg daily in divided doses,  after foodPR: 100 mg twice daily if required Gout: 150\u2013200 mg daily in divided doses Dysmenorrhoea: up to 75 mg daily Maximum combined oral and PR: 150\u2013 200 mg 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 :357.8<\/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 :90\u201399<\/li>\n<li>  %Excreted unchanged in urine &amp;nbsp &amp;nbsp : 5\u201320 (60% as metabolites)<\/li>\n<p><LI> Volume of distribution (L\/kg) &amp;nbsp &amp;nbsp &amp;nbsp :0.34\u20131.57<\/li>\n<p><LI>half-life \u2013 normal\/ESRD (hrs)&amp;nbsp &amp;nbsp &amp;nbsp :1\u201316\/unchanged<H3>  DOSE IN RENAL IMPAIRMENT <\/H3> <H4>GFR (mL\/MIN)<\/H4><LI> 20 to 50  &amp;nbsp &amp;nbsp : Dose as in normal renal function, but avoid if possible<LI> 10 to 20  &amp;nbsp &amp;nbsp : 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 CKD 5 and 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:Not 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 :Not dialysed. Dose as in normal renal function <LI>HDF\/high flux  &amp;nbsp :Unlikely to be dialysed. Dose as in normal renal function <LI>CAV\/VVHD  &amp;nbsp &amp;nbsp &amp;nbsp:Not dialysed. Dose as in GFR=10\u201320 mL\/min<H3> IMPORTANT DRUG INTERACTIONS  <\/H3>Potentially hazardous interactions with other drugsACE 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 and  phenindione enhanced; possibly increased risk of bleeding with heparins\n<li>Antidepressants: increased risk of bleeding  with SSRIs and venlafaxineAntidiabetic agents: effects of  sulphonylureas enhancedAnti-epileptic agents: effects of phenytoin  enhanced\n<li>Antipsychotics: possible severe drowsiness  with haloperidol\n<li>Antivirals:  increased risk of haematological  toxicity with zidovudine; concentration possibly increased by ritonavir\n<li>Ciclosporin: increased risk of  nephrotoxicityCytotoxic agents: reduced excretion of  methotrexate\n<li>    Diuretics: increased risk of nephrotoxicity,  hyperkalaemia with potassium-sparing diuretics; antagonism of diuretic effect\n<li> Lithium: lithium excretion reduced Pentoxifylline: possibly increased risk of  bleedingProbenecid: excretion of indometacin  reduced\n<li>  Tacrolimus: increased risk of  nephrotoxicity<H3> ADMINISTRATION  <\/H3><H4> Reconstition<\/H4>\u2013<H4>  Route  <\/H4>Oral, PR, IV <H4>  Rate of Administration  <\/H4>20\u201330 minutes <H4>Comments<\/H4>\u2013.382 indoMETACin<H4>  OTHER INFORMATION  <\/H4>Inhibition of renal prostaglandin synthesis  by NSAIDs may interfere with renal function, especially in the presence of existing renal disease \u2013 avoid if possible; if not, check serum creatinine 48\u201372 hours after starting NSAID \u2013 if raised, discontinue NSAID therapyUse normal doses in patients with ERF on  dialysis if they do not pass any urineUse with caution in renal transplant  recipients \u2013 can reduce intrarenal autocoid synthesis.<br \/>\n","protected":false},"excerpt":{"rendered":"<p>indometacin CLINICAL USE NSAID:Pain and inflammation in rheumatic disease and<\/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-4532","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\/4532","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=4532"}],"version-history":[{"count":0,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/posts\/4532\/revisions"}],"wp:attachment":[{"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/media?parent=4532"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/categories?post=4532"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/tags?post=4532"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}