{"id":2290,"date":"2023-06-25T17:55:36","date_gmt":"2023-06-25T17:55:36","guid":{"rendered":"https:\/\/kidneydiseaseclinic.net\/kdc\/zidovudine\/"},"modified":"2023-06-25T18:00:40","modified_gmt":"2023-06-25T18:00:40","slug":"zidovudine","status":"publish","type":"post","link":"https:\/\/kidneydiseaseclinic.net\/kdc\/zidovudine\/","title":{"rendered":"Zidovudine"},"content":{"rendered":"<p><img decoding=\"async\" src=\"https:\/\/kidneydiseaseclinic.net\/renaldrugs\/img\/Zidovudine.JPG\"><\/p>\n<h3>  CLINICAL USE<\/h3>\n<p>Nucleoside reverse transcriptase inhibitor: Treatment of HIV in combination with   other antiretroviral drugs Prevention of maternal-foetal HIV   transmission<\/p>\n<h3> DOSE IN NORMAL RENAL FUNCTION<\/h3>\n<p>Oral: 500\u2013600 mg daily in 2\u20133 divided doses IV: 1\u20132 mg\/kg every 4 hours<\/p>\n<h3>  PHARMACOKINETICS<\/h3>\n<li> Molecular weight &nbsp;  &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;  &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; : 267.2<\/li>\n<li>  %Protein binding  &nbsp; &nbsp; &nbsp;  &nbsp;  &nbsp;  &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; : 34\u201338<\/li>\n<li>  %Excreted unchanged in urine &nbsp; &nbsp; : 8\u201325<\/li>\n<li> Volume of distribution (L\/kg) &nbsp; &nbsp; &nbsp; : 1.6<\/li>\n<li>half-life \u2013 normal\/ESRD (hrs)&nbsp; &nbsp; &nbsp; : 1.1\/1. 4\u20133<br \/>\n<h3>  DOSE IN RENAL IMPAIRMENT<\/h3>\n<h4>GFR (mL\/MIN)<\/h4>\n<\/li>\n<li> 20 to 50  &nbsp; &nbsp; : Give 100% of normal dose every 8 hours<\/li>\n<li> 10 to 20  &nbsp; &nbsp; : Give 100% of normal dose every 8 hours<\/li>\n<li> &lt;10 &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; : Give 50% of normal dose every 8 hours1<br \/>\n<h3> DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES<\/h3>\n<\/li>\n<li> CAPD  &nbsp; &nbsp; &nbsp;  &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;: Not dialysed. Dose as in GFR &lt;10 mL\/min<\/li>\n<li> HD &nbsp;  &nbsp; &nbsp;  &nbsp; &nbsp;  &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; : Not dialysed. Dose as in GFR &lt;10 mL\/min Give post dialysis<\/li>\n<li>HDF\/high flux  &nbsp; : Unknown dialysability. Dose as in GFR &lt;10 mL\/min Give post dialysis<\/li>\n<li>CAV\/VVHD  &nbsp; &nbsp; &nbsp;: Not dialysed. Dose as in GFR 10 to 20   mL\/min<br \/>\n<h3> IMPORTANT DRUG INTERACTIONS<\/h3>\n<p>Potentially hazardous interactions with other drugs<\/li>\n<li>Antibacterials: absorption reduced by   clarithromycin; avoid concomitant use with rifampicin<\/li>\n<li>Anti-epileptics: phenytoin levels may be   raised or lowered; concentration possibly increased by valproate (increased risk of toxicity)<\/li>\n<li>  Antifungals: concentration increased by   fluconazole<\/li>\n<li>Antivirals:  profound myelosuppression   with ganciclovir \u2013 avoid if possible; extreme lethargy on administration of IV aciclovir; effects of stavudine inhibited \u2013 avoid concomitant use; concentration reduced by tipranavir<br \/>\n<h3> ADMINISTRATION<\/h3>\n<h4> Reconstition<\/h4>\n<p>&#8211;<\/p>\n<h4>  Route<\/h4>\n<p>IV, oral<\/p>\n<h4>  Rate of Administration<\/h4>\n<p>1 hour<\/p>\n<h4>Comments<\/h4>\n<p>Dilute with glucose 5% infusion to give a   final concentration of 2 mg\/mL or 4 mg\/mL<\/p>\n<h4>  OTHER INFORMATION<\/h4>\n<p>Dialysis has little effect on zidovudine,   presumably because of rapid metabolism. The glucuronide metabolite (T\u00bd =1 hour) has no antiviral activity and will be significantly removed by dialysis Patients with severe renal failure have 50%   higher maximum plasma concentrations 90% of a dose is excreted renally, mostly   as the glucuronide. There is substantial accumulation of this metabolite in renal failure Main risk in renal impairment is   haematological toxicity<\/li>\n","protected":false},"excerpt":{"rendered":"<p>CLINICAL USE Nucleoside reverse transcriptase inhibitor: Treatment of HIV in<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[7],"class_list":["post-2290","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\/2290","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=2290"}],"version-history":[{"count":1,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/posts\/2290\/revisions"}],"predecessor-version":[{"id":2304,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/posts\/2290\/revisions\/2304"}],"wp:attachment":[{"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/media?parent=2290"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/categories?post=2290"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/tags?post=2290"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}