{"id":4002,"date":"2025-03-31T18:11:55","date_gmt":"2025-03-31T18:11:55","guid":{"rendered":"https:\/\/kidneydiseaseclinic.net\/kdc\/flupentixol-txt\/"},"modified":"2025-03-31T18:11:55","modified_gmt":"2025-03-31T18:11:55","slug":"flupentixol-txt","status":"publish","type":"post","link":"https:\/\/kidneydiseaseclinic.net\/kdc\/flupentixol-txt\/","title":{"rendered":"Flupentixol.txt"},"content":{"rendered":"<h1>  Flupentixol   <\/h1>\n<p><H3>  CLINICAL USE <\/H3><br \/>\nAntipsychotic:Schizophrenia and other psychoses Depression <H3> DOSE IN NORMAL RENAL FUNCTION  <\/H3>Psychosis: Oral: 3\u20139 mg twice daily \u2014Deep IM: 50 mg 4 weekly \u2013 300 mg 2  \u2014weekly; maximum dose 400 mg weekly; 20\u201340 mg every 2\u20134 weeks may be adequate in some patientsDepression: 0.5\u20133 mg daily (doses above  2 mg should be in 2 divided doses, and 2nd dose should not be after 4 pm)<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 :434.5 (588.8 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 :&gt;95<\/li>\n<li>  %Excreted unchanged in urine &amp;nbsp &amp;nbsp : Negligible<\/li>\n<p><LI> Volume of distribution (L\/kg) &amp;nbsp &amp;nbsp &amp;nbsp :12\u201314<\/li>\n<p><LI>half-life \u2013 normal\/ESRD (hrs)&amp;nbsp &amp;nbsp &amp;nbsp :22\u201336 (IM: 3\u20138 days)\/Increased<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 quarter to half 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>Alcohol: enhanced effects\n<li>     Anaesthetics: enhanced hypotensive  effects\n<li>Analgesics: increased risk of convulsions  with tramadol; enhanced hypotensive and sedative effects with opioids\n<li>Antidepressants: increased plasma 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 ritonavirAnxiolytics and hypnotics: increased  sedative effects\n<li>Sibutramine: increased risk of CNS  toxicity \u2013 avoid concomitant useAvoid 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 sedation in  renal impairmentIncreased CNS sensitivity in renally  impaired patients \u2013 start with small doses as can accumulateFor IM injection a 20 mg test dose should  first be givenOral bioavailability is 40\u201355% Peak levels occur 7 days after IM injection  and 4 hours after oral administration.<br \/>\n","protected":false},"excerpt":{"rendered":"<p>Flupentixol CLINICAL USE Antipsychotic:Schizophrenia and other psychoses Depression 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-4002","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\/4002","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=4002"}],"version-history":[{"count":0,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/posts\/4002\/revisions"}],"wp:attachment":[{"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/media?parent=4002"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/categories?post=4002"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/tags?post=4002"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}