{"id":4486,"date":"2025-03-31T18:12:10","date_gmt":"2025-03-31T18:12:10","guid":{"rendered":"https:\/\/kidneydiseaseclinic.net\/kdc\/zuclopenthixol-txt\/"},"modified":"2025-03-31T18:12:10","modified_gmt":"2025-03-31T18:12:10","slug":"zuclopenthixol-txt","status":"publish","type":"post","link":"https:\/\/kidneydiseaseclinic.net\/kdc\/zuclopenthixol-txt\/","title":{"rendered":"Zuclopenthixol.txt"},"content":{"rendered":"<p><H3>  CLINICAL USE <\/H3>  Antipsychotic for schizophrenia and other psychoses <H3> DOSE IN NORMAL RENAL FUNCTION  <\/H3> Schizophrenia and paranoid psychoses: Oral: 20\u201330 mg daily in divided doses;   maximum 150 mg daily Maintenance: <LI> 20 to 50  &amp;nbsp &amp;nbsp : mg daily   Deep IM: 200\u2013500 mg every 1\u20134 weeks   Maximum: 600 mg weekly   Acute psychoses: (Clopixol Acuphase) Deep IM: 50\u2013150 mg, repeated if required   after 2\u20133 days Maximum 400 mg per course   <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 : 401 (443 as acetate), (473.9 as hydrochloride), (555.2 as decanoate) <\/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 : 98 <\/li>\n<li>  %Excreted unchanged in urine &amp;nbsp &amp;nbsp : Minimal (<LI> 10 to 20   <\/LI>% unchanged drug and metabolites) <\/li>\n<p><LI> Volume of distribution (L\/kg) &amp;nbsp &amp;nbsp &amp;nbsp : <LI> 10 to 20  &amp;nbsp &amp;nbsp : <\/li>\n<p><LI>half-life \u2013 normal\/ESRD (hrs)&amp;nbsp &amp;nbsp &amp;nbsp : 20\u201324 <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 <LI> 10 to 20  &amp;nbsp &amp;nbsp : Dose as in normal renal function <LI> &lt;10 &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp : Start with 50% of the dose 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: Not 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: Not dialysed. Dose as in normal renal function <H3> IMPORTANT DRUG INTERACTIONS  <\/H3> Potentially hazardous interactions with other drugs\n<li>     Anaesthetics: enhanced hypotensive   effects\n<li>Analgesics: increased risk of convulsions   with tramadol; enhanced hypotensive and sedative effects with opioids\n<li>Anti-arrhythmics: increased risk of   ventricular arrhythmias with anti- arrhythmics that prolong the QT interval\n<li>Antidepressants: increased level of   tricyclics\n<li>Anti-epileptics: anticonvulsant effect   antagonised\n<li>Antimalarials: avoid concomitant use with   artemether\/lumefantrine\n<li>Antipsychotics: avoid concomitant use of   clozapine with depot preparations in case of neutropenia\n<li>Antivirals:  concentration possibly   increased with ritonavir Anxiolytics and hypnotics: increased   sedative effects\n<li>Sibutramine: increased risk of CNS   toxicity \u2013 avoid concomitant use Avoid concomitant use with drugs that   prolong the QT interval <H3> ADMINISTRATION  <\/H3> <H4> Reconstition<\/H4> \u2013 <H4>  Route  <\/H4> Oral, IM   <H4>  Rate of Administration  <\/H4> \u2013 <H4>Comments<\/H4> \u2013 <H4>  OTHER INFORMATION  <\/H4> May cause hypotension and excessive   sedation Increased CNS sensitivity in renally   impaired patients \u2013 start with small doses as can accumulate Peak levels occur 3\u20136 hours after oral   administration .the liver. It can be used in renal failure at normal doses with caution.<br \/>\n","protected":false},"excerpt":{"rendered":"<p>CLINICAL USE Antipsychotic for schizophrenia and other psychoses 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-4486","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\/4486","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=4486"}],"version-history":[{"count":0,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/posts\/4486\/revisions"}],"wp:attachment":[{"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/media?parent=4486"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/categories?post=4486"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/tags?post=4486"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}