{"id":4634,"date":"2025-03-31T18:12:15","date_gmt":"2025-03-31T18:12:15","guid":{"rendered":"https:\/\/kidneydiseaseclinic.net\/kdc\/procainamide-hydrochloride-txt\/"},"modified":"2025-03-31T18:12:15","modified_gmt":"2025-03-31T18:12:15","slug":"procainamide-hydrochloride-txt","status":"publish","type":"post","link":"https:\/\/kidneydiseaseclinic.net\/kdc\/procainamide-hydrochloride-txt\/","title":{"rendered":"procainamide hydrochloride.txt"},"content":{"rendered":"<p><H3>  CLINICAL USE <\/H3><br \/>\nAnti-arrhythmic agent:Treatment of ventricular arrhythmias,  especially after myocardial infarctionAtrial tachycardia <H3> DOSE IN NORMAL RENAL FUNCTION  <\/H3>Slow IV injection: 50 mg\/min (100 mg with  ECG monitoring), repeated at 5-minute intervals until arrhythmia is controlled; max dose 1 gInfusion: 500\u2013600 mg over 25\u201330 minutes  with ECG monitoring, then maintenance of 2\u20136 mg\/minute. If required start oral anti-arrhythmics 3\u20134 hours after infusion<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 :271.8<\/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 :15\u201320<\/li>\n<li>  %Excreted unchanged in urine &amp;nbsp &amp;nbsp : 30\u201370<\/li>\n<p><LI> Volume of distribution (L\/kg) &amp;nbsp &amp;nbsp &amp;nbsp :1.48\u20134.3<\/li>\n<p><LI>half-life \u2013 normal\/ESRD (hrs)&amp;nbsp &amp;nbsp &amp;nbsp :2.5\u20135\/9.6\u201311.3<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 : Normal loading dose. Maintenance dose according to response, lower doses or longer dosage intervals may be required<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. Dose as in GFR<LI> &lt;10 &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp : 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 :Dialysed. Dose as in GFR<LI> &lt;10 &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp : mL\/min <LI>HDF\/high flux  &amp;nbsp :Dialysed. Dose as in GFR<LI> &lt;10 &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp : mL\/min<LI>CAV\/VVHD  &amp;nbsp &amp;nbsp &amp;nbsp:Dialysed. Dose as in normal renal function<H3> IMPORTANT DRUG INTERACTIONS  <\/H3>Potentially hazardous interactions with other drugs\n<li>Anti-arrhythmics: amiodarone increases  procainamide levels, increased risk of ventricular arrhythmias \u2013 avoid concomitant use; increased myocardial depression with other anti-arrhythmics\n<li>Antibacterials: increased risk of  ventricular arrhythmias with moxifloxacin \u2013 avoid concomitant use; concentration increased by trimethoprim\n<li>Antidepressants: increased risk of  ventricular arrhythmias with tricyclicsAntihistamines: increased risk of  ventricular arrhythmias with mizolastine\u2013 avoid concomitant use\n<li>Antimalarials: increased risk of ventricular  arrhythmias with artemether\/lumefantrine \u2013 avoid concomitant use\n<li>Antipsychotics: increased risk  of ventricular arrhythmias with phenothiazines and any antipsychotics that prolong the QT interval; avoid with amisulpride, pimozide and sertindole\n<li>Atomoxetine: increased risk of ventricular  arrhythmias\n<li>Beta-blockers: increased myocardial  depression; increased risk of ventricular arrhythmias with sotalol \u2013 avoid concomitant use5HT 3 antagonists: increased risk of ventricular arrhythmias with dolasetron \u2013 avoid concomitant use; avoid with tropisetronMuscle relaxants: enhanced effect of  muscle relaxants\n<li> Ulcer-healing drugs: levels increased by  cimetidine<H3> ADMINISTRATION  <\/H3><H4> Reconstition<\/H4>\u2013<H4>  Route  <\/H4>IV bolus, <H4> IV infusion  <\/H4>, IM <H4>  Rate of Administration  <\/H4>Bolus: 50\u2013100 mg\/minute Infusion: 2\u20136 mg\/minute <H4>Comments<\/H4>Stable in glucose 5% Dilute to a concentration of 2 mg\/mL and  give at a rate of 1\u20133 mL\/minute, or to a Procainamide hydrochloride.PROCAINAMIDe HYDROCHLORIDe 607concentration of 4 mg\/mL and give at a rate of 0.5\u20131.5 mL\/minuteStability of solution can be improved by  adding sodium bicarbonate to glucose solution<H4>  OTHER INFORMATION  <\/H4>For optimum response, plasma  concentration should be 3\u201310 mg\/L; severe toxicity has been noted at concentrations above 12 mg\/LActive metabolite is N-acetyl- procainamide (NAPA) which is 80% renally excretedHaemofiltration can be used in cases of  procainamide poisoningHalf-life depends on acetylator status of  patientCan cause systemic lupus erythematosus  in up to 30% of patients with long-term use CAPD  removes 19% of procainamide and  24% of NAPA.<br \/>\n","protected":false},"excerpt":{"rendered":"<p>CLINICAL USE Anti-arrhythmic agent:Treatment of ventricular arrhythmias, especially after myocardial<\/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-4634","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\/4634","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=4634"}],"version-history":[{"count":0,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/posts\/4634\/revisions"}],"wp:attachment":[{"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/media?parent=4634"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/categories?post=4634"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/tags?post=4634"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}