rifampicin
rifampicin.JPG

CLINICAL USE

Antibacterial agent:Tuberculosis Staphylococcal infection

DOSE IN NORMAL RENAL FUNCTION

600–1200 mg daily in 2–4 divided doses

PHARMACOKINETICS

  • Molecular weight                           :822.9
  • %Protein binding                           :80
  • %Excreted unchanged in urine     : 15–30
  • Volume of distribution (L/kg)       :0.64–0.66
  • half-life – normal/ESRD (hrs)      :2–5/1.8–11

    DOSE IN RENAL IMPAIRMENT

    GFR (mL/MIN)

  • 20 to 50     : Dose as in normal renal function
  • 10 to 20     : Dose as in normal renal function
  • <10           : 50% – 100% of normal dose

    DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES

  • CAPD                :Not dialysed. Dose as in GFR <10 mL/min
  • HD                     :Not dialysed. Dose as in GFR <10 mL/min
  • HDF/high flux   :Not dialysed. Dose as in GFR <10 mL/min
  • CAV/VVHD      :Unknown dialysability. Dose as in normal renal function

    IMPORTANT DRUG INTERACTIONS

    Potentially hazardous interactions with other drugs
  • Anti-arrhythmics: metabolism of disopyramide, mexiletine and propafenone accelerated
  • Antibacterials: reduced concentration of chloramphenicol, clarithromycin, dapsone, trimethoprim and telithromycin – avoid with telithromycin; monitor LFTs in combination with quinupristin/dalfopristin; concentration increased by clarithromycin and other macrolides
  • Anticoagulants: reduced anticoagulant effect of coumarinsAntidiabetics: reduced antidiabetic effect of chlorpropamide and tolbutamide; concentration of rosiglitazone, nateglinide and repaglinide reduced – may need to increase dose of rosiglitazone; possibly reduced antidiabetic effect with sulphonylureas
  • Anti-epileptics: reduced concentration of phenytoin and lamotrigine
  • Antifungals: concentration of both drugs may be reduced with ketoconazole; reduced concentration of fluconazole, itraconazole, posaconazole and terbinafine; concentration of voriconazole reduced – avoid concomitant use; initially increases then reduces caspofungin concentration
  • Antipsychotics: reduced concentration of haloperidol, aripiprazole and clozapine – increase dose of aripiprazole
  • Antivirals: concentration of abacavir and tipranavir possibly reduced – avoid with tipranavir; concentration of amprenavir, atazanavir, darunavir, indinavir, lopinavir, nelfinavir, nevirapine and saquinavir reduced – avoid; concentration of efavirenz reduced – increase dose of efavirenz; avoid with zidovudineAtovaquone: concentration of atovaquone reduced (possible therapeutic failure of atovaquone)Bosentan: reduced bosentan concentration – avoid
  • Calcium-channel blockers: metabolism of diltiazem, verapamil, isradipine, nicardipine, nifedipine, nisoldipine and nimodipine accelerated
  • Ciclosporin: markedly reduced levels (danger of transplant rejection); ciclosporin dose may need increasing 5-fold or moreCorticosteroids: reduced level of corticosteroids – double steroid dose. Give as twice daily dosageCytotoxics: reduced concentration of erlotinib, sunitinib, dasatinib and imatinib – avoid with imatinib
  • Diuretics: concentration of eplerenone reduced – avoidOestrogens and progestogens: reduced contraceptive effect due to increased metabolism
  • Tacrolimus: reduced tacrolimus concentrationSirolimus: reduced sirolimus concentration.646 riFAMPiCin

    ADMINISTRATION

    Reconstition

    Use solvent provided

    Route

    Oral, IV

    Rate of Administration

    2–3 hours

    Comments

    Dilute in 500 mL glucose 5% or sodium chloride 0.9%For central administration, 600 mg in 100 mL glucose 5% over 0.5–2 hours has been used (unlicensed). Stable for up to 24 hours at room temperature

    OTHER INFORMATION

    Some units give dose in concentrations up to 60 mg/mL (in its own solvent) over 10 minutes, on prescriber’s responsibilityMay cause acute interstitial nephritis, potassium wasting or renal tubular defectsReduce dose if LFTs are abnormal or patient <45 kgAbsorption from gastrointestinal tract can be reduced by up to 80% by the presence of food in the gastrointestinal tract
    CAPD exit site infections: 300 mg twice daily for 4 weeks has been usedRifampicin is excreted into
    CAPD fluid causing an orange/yellow colourMonitor rifampicin levels if necessary In severe renal impairment there is no increase in half-life at doses less than 600 mg daily.



    See how to identify renal failure stages according to GFR calculation

    See how to diagnose irreversible renal disease

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