dornase alfa

CLINICAL USE

To improve pulmonary function in cystic fibrosis

DOSE IN NORMAL RENAL FUNCTION

2.5 mg (2500 u) daily via nebuliser can be increased to twice daily if over 21 years of age

PHARMACOKINETICS

  • Molecular weight                           :29 249.6
  • %Protein binding                           :No data
  • %Excreted unchanged in urine     : No data
  • Volume of distribution (L/kg)       :No data
  • half-life – normal/ESRD (hrs)      :11 (from lungs in rats)

    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           : Dose as in normal renal function

    DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES

  • CAPD                :Unlikely to be dialysed. Dose as in normal renal function
  • HD                     :Unlikely to be dialysed. Dose as in normal renal function
  • HDF/high flux   :Unlikely to be dialysed. Dose as in normal renal function
  • CAV/VVHD      :Unlikely to be dialysed. Dose as in normal renal function

    IMPORTANT DRUG INTERACTIONS

    Potentially hazardous interactions with other drugs

  • None known

    ADMINISTRATION

    Reconstition

    Route

    Nebulised

    Rate of Administration

    Comments

    <15% of dose is systemically absorbed

    OTHER INFORMATION

    No pharmacokinetic data available; little systemic absorption therefore little accumulation expectedUse undiluted, using recommended jet nebuliser/compressor system.

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