Temocillin
Temocillin.JPG

CLINICAL USE

Antibacterial agent

DOSE IN NORMAL RENAL FUNCTION

1–2 g every 12 hoursAcute uncomplicated UTIs: 1 g daily in a single or divided doses

PHARMACOKINETICS

  • Molecular weight                           :458.4 (as sodium salt)
  • %Protein binding                           :75–85
  • %Excreted unchanged in urine     : 90
  • Volume of distribution (L/kg)       :0.23
  • half-life – normal/ESRD (hrs)      :3.1–5.4/28.2

    DOSE IN RENAL IMPAIRMENT

    GFR (mL/MIN)

    30–50 Dose as in normal renal function 10–30 1–2 g daily
  • <10           : 1–2 g every 48 hours

    DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES

  • CAPD                :Not dialysed. Dose as in GFR <10 mL/min
  • HD                     :Dialysed. Dose as in GFR <10 mL/min
  • HDF/high flux   :Dialysed. Dose as in GFR <10 mL/min
  • CAV/VVHD      :Dialysed. Dose as in GFR=10–30 mL/min

    IMPORTANT DRUG INTERACTIONS

    Potentially hazardous interactions with other drugsTemocillin can reduce the excretion of methotrexate (increased risk of toxicity)

    ADMINISTRATION

    Reconstition

    IV: Dissolve in 20 mL water for injection

    IV infusion

    : Dilute in 50–100 mL sodium chloride 0.9%IM: Dissolve in 2 mL water for injection or lidocaine 0.5–1% (volume 2.7 mL)

    Route

    IV, IM

    Rate of Administration

    Slow IV bolus over 3–4 minutes Infusion over 30–40 minutes

    Comments

    Incompatible with proteins, blood products, lipid emulsions and aminoglycosides

    OTHER INFORMATION

    Bleeding has occurred in some patients (more likely in those with renal impairment)20% is removed by haemodialysis and 17–26% by peritoneal dialysis.



    See how to identify renal failure stages according to GFR calculation

    See how to diagnose irreversible renal disease

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