{"id":4580,"date":"2025-03-31T18:12:13","date_gmt":"2025-03-31T18:12:13","guid":{"rendered":"https:\/\/kidneydiseaseclinic.net\/kdc\/netilmicin-txt\/"},"modified":"2025-03-31T18:12:13","modified_gmt":"2025-03-31T18:12:13","slug":"netilmicin-txt","status":"publish","type":"post","link":"https:\/\/kidneydiseaseclinic.net\/kdc\/netilmicin-txt\/","title":{"rendered":"netilmicin.txt"},"content":{"rendered":"<p><H3>  CLINICAL USE <\/H3><br \/>\nAntibacterial agent<H3> DOSE IN NORMAL RENAL FUNCTION  <\/H3>IM, IV: 4\u20137.5 mg\/kg daily, as a single  daily dose or in divided doses every 8 or 12 hoursUrinary tract infection: 150 mg daily for  5 days<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 :1441.6 (as sulphate)<\/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 :&lt;5<\/li>\n<li>  %Excreted unchanged in urine &amp;nbsp &amp;nbsp : 80<\/li>\n<p><LI> Volume of distribution (L\/kg) &amp;nbsp &amp;nbsp &amp;nbsp :0.16\u20130.3<\/li>\n<p><LI>half-life \u2013 normal\/ESRD (hrs)&amp;nbsp &amp;nbsp &amp;nbsp :2\u20132.5\/35\u201372<H3>  DOSE IN RENAL IMPAIRMENT <\/H3> <H4>GFR (mL\/MIN)<\/H4><LI> 20 to 50  &amp;nbsp &amp;nbsp : 4\u20137.5 mg\/kg once daily. Monitor levels<LI> 10 to 20  &amp;nbsp &amp;nbsp : 3\u20134 mg\/kg once daily. Monitor levels<LI> &lt;10 &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp : 2 mg\/kg once daily. Monitor levels<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:Dialysed. IV: 2 mg\/kg on alternate daysIP: 7.5\u201310 mg\/L per exchange. Monitor levels<\/p>\n<li> HD &amp;nbsp  &amp;nbsp &amp;nbsp  &amp;nbsp &amp;nbsp  &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp :Dialysed. Administer 2 mg\/kg at the end of each dialysis session. Monitor levels<LI>HDF\/high flux  &amp;nbsp :Dialysed. Administer 2 mg\/kg at the end of each dialysis session. Monitor levels<LI>CAV\/VVHD  &amp;nbsp &amp;nbsp &amp;nbsp:Dialysed. Dose as in GFR=10\u201320 mL\/min. Monitor levels<H3> IMPORTANT DRUG INTERACTIONS  <\/H3>Potentially hazardous interactions with other drugsBotulinum toxin: neuromuscular block  enhanced (risk of toxicity)\n<li>Ciclosporin: increased risk of  nephrotoxicityCytotoxics: increased risk of  nephrotoxicity and possibly of ototoxicity with platinum compounds\n<li>    Diuretics: increased risk of ototoxicity  with loop diureticsMuscle relaxants: effects of non- depolarising muscle relaxants and suxamethonium enhancedParasympathomimetics: antagonism of  effect of neostigmine and pyridostigmine\n<li>  Tacrolimus: increased risk of  nephrotoxicity<H3> ADMINISTRATION  <\/H3><H4> Reconstition<\/H4>\u2013<H4>  Route  <\/H4>IM, IP, IV bolus or infusion <H4>  Rate of Administration  <\/H4>IV bolus: Administer over 3\u20135 minutes <H4> IV infusion  <\/H4>: Administer over 0.5\u20132 hours <H4>Comments<\/H4>Add to 50\u2013200 mL of sterile water for  injection, sodium chloride 0.9%, glucose 5% or 10%IM and IV dose are identical. Calculate  on mg\/kg lean body weight, or actual weight, whichever is lower<H4>  OTHER INFORMATION  <\/H4>Netilmicin serum concentrations should  be monitored and used for basis of dosage adjustment, otherwise follow guidelines in the SPC according to serum creatinine\/creatinine clearanceOnce-daily administration of netilmicin  may lead to transient peak concentrations of 20\u201330 micrograms\/mL. Other dosage regimens will result in peak levels not exceeding 12 micrograms\/mL. Prolonged levels above 16 micrograms\/mL should be avoided. If trough levels are monitored they will usually be 3 micrograms\/mL or less with the recommended dosage. Increasing trough concentrations above 4 micrograms\/mL should be avoided.<br \/>\n","protected":false},"excerpt":{"rendered":"<p>CLINICAL USE Antibacterial agent DOSE IN NORMAL RENAL FUNCTION IM,<\/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-4580","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\/4580","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=4580"}],"version-history":[{"count":0,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/posts\/4580\/revisions"}],"wp:attachment":[{"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/media?parent=4580"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/categories?post=4580"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/tags?post=4580"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}