{"id":4284,"date":"2025-03-31T18:12:03","date_gmt":"2025-03-31T18:12:03","guid":{"rendered":"https:\/\/kidneydiseaseclinic.net\/kdc\/paroxetine-txt\/"},"modified":"2025-03-31T18:12:03","modified_gmt":"2025-03-31T18:12:03","slug":"paroxetine-txt","status":"publish","type":"post","link":"https:\/\/kidneydiseaseclinic.net\/kdc\/paroxetine-txt\/","title":{"rendered":"Paroxetine.txt"},"content":{"rendered":"<p><H3>  CLINICAL USE <\/H3><br \/>\nAntidepressant:Panic disorders Obsessive compulsive disorder Social anxiety Post traumatic stress disorder <H3> DOSE IN NORMAL RENAL FUNCTION  <\/H3>10\u201360 mg daily depending on indication<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 :329.4<\/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 :95<\/li>\n<li>  %Excreted unchanged in urine &amp;nbsp &amp;nbsp : &lt;2<\/li>\n<p><LI> Volume of distribution (L\/kg) &amp;nbsp &amp;nbsp &amp;nbsp :13<\/li>\n<p><LI>half-life \u2013 normal\/ESRD (hrs)&amp;nbsp &amp;nbsp &amp;nbsp :24\/30<H3>  DOSE IN RENAL IMPAIRMENT <\/H3> <H4>GFR (mL\/MIN)<\/H4>30\u201350 Dose as in normal renal function10\u201330 20 mg daily and titrate slowly<LI> &lt;10 &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp : 20 mg daily and titrate slowly<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 GFR &lt;10 mL\/min <\/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 GFR &lt;10 mL\/min <LI>HDF\/high flux  &amp;nbsp :Unknown dialysability. Dose as in GFR &lt;10 mL\/min<LI>CAV\/VVHD  &amp;nbsp &amp;nbsp &amp;nbsp:Unknown dialysability. Dose as for GFR=10\u201330 mL\/min<H3> IMPORTANT DRUG INTERACTIONS  <\/H3>Potentially hazardous interactions with other drugs\n<li>Analgesics: increased risk of bleeding with  aspirin and NSAIDs; increased risk of CNS toxicity with tramadol\n<li>Anti-arrhythmics: possibly inhibits  propafenone metabolism (increased risk of toxicity)\n<li>Anticoagulants: effect of coumarins  possibly enhanced\n<li>Antidepressants: avoid concomitant use  with MAOIs and moclobemide (increased risk of toxicity); avoid concomitant use with St John\u2019s wort; possibly enhanced serotonergic effects with duloxetine; can increase tricyclics antidepressant concentration; increased agitation and nausea with tryptophan\n<li>Anti-epileptics: antagonism (lowered  convulsive threshold); concentration reduced by carbamazepine, phenytoin and primidone\n<li>Antimalarials: avoid concomitant use with  artemether\/lumefantrine\n<li>Antipsychotics: concentration of  clozapine, sertindole and possibly risperidone increased; metabolism of perphenazine inhibited, reduce dose of perphenazine; possibly inhibit aripiprazole metabolism, reduce aripiprazole dose\n<li>Antivirals:  concentration increased by  ritonavir\n<li>Dopaminergics: use entacapone with  caution; increased risk of hypertension and CNS excitation with selegiline \u2013 avoid concomitant use; increased risk of CNS toxicity with rasagiline \u2013 avoid concomitant use5HT 1 agonist: risk of CNS toxicity increased by sumatriptan \u2013 avoid concomitant use; possibly increased risk of serotonergic effects with frovatriptan\n<li> Lithium: increased risk of CNS effects \u2013  monitor levels\n<li>Sibutramine: increased risk of CNS  toxicity \u2013 avoid concomitant use<H3> ADMINISTRATION  <\/H3><H4> Reconstition<\/H4>\u2013<H4>  Route  <\/H4>Oral <H4>  Rate of Administration  <\/H4>\u2013<H4>Comments<\/H4>\u2013<br \/>\n","protected":false},"excerpt":{"rendered":"<p>CLINICAL USE Antidepressant:Panic disorders Obsessive compulsive disorder Social anxiety Post<\/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-4284","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\/4284","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=4284"}],"version-history":[{"count":0,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/posts\/4284\/revisions"}],"wp:attachment":[{"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/media?parent=4284"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/categories?post=4284"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/tags?post=4284"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}