CLINICAL USE

Antibacterial agent

DOSE IN NORMAL RENAL FUNCTION

1–2 g daily

PHARMACOKINETICS

  • Molecular weight &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp : 247.3
  • %Protein binding &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp : 8–121
  • %Excreted unchanged in urine &nbsp &nbsp : 20–25
  • Volume of distribution (L/kg) &nbsp &nbsp &nbsp : 0.61–0.671
  • half-life – normal/ESRD (hrs)&nbsp &nbsp &nbsp : 12–14/Unchanged

    DOSE IN RENAL IMPAIRMENT

    GFR (mL/MIN)

  • 20 to 50 &nbsp &nbsp : Dose as in normal renal function
  • 10 to 20 &nbsp &nbsp : Dose as in normal renal function
  • <10 &nbsp &nbsp &nbsp &nbsp &nbsp : Dose as in normal renal function

    DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES

  • CAPD &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp: Unknown dialysability, but likely to be dialysed. Dose as in normal renal function

  • HD &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp : Dialysed. Dose as in normal renal function
  • HDF/high flux &nbsp : Dialysed. Dose as in normal renal function
  • CAV/VVHD &nbsp &nbsp &nbsp: Unknown dialysability. Dose as in normal renal function

    IMPORTANT DRUG INTERACTIONS

    Potentially hazardous interactions with other drugs
  • Alcohol: disulfiram-like reaction

    ADMINISTRATION

    Reconstition

    Route

    Oral

    Rate of Administration

    Comments

    OTHER INFORMATION

    Dosage adjustment in renal failure is not necessary as a decrease in renal clearance is compensated for by increased faecal excretion of tinidazole 43% can be removed during a 6 hour haemodialysis session. .