moxisylyte
moxisylyte.JPG

CLINICAL USE

Primary Raynaud’s syndrome

DOSE IN NORMAL RENAL FUNCTION

40–80 mg 4 times daily

PHARMACOKINETICS

  • Molecular weight                           :315.8
  • %Protein binding                           :No data
  • %Excreted unchanged in urine     : <1
  • Volume of distribution (L/kg)       :Low1
  • half-life – normal/ESRD (hrs)      :1–2

    DOSE IN RENAL IMPAIRMENT

    GFR (mL/MIN)

    25–50 Dose as in normal renal function10–25 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 drugsAlpha-blockers: possibly severe postural hypotension when given in combination
  • Beta-blockers: possibly severe postural hypotension when given in combination

    ADMINISTRATION

    Reconstition

    Route

    Oral

    Rate of Administration

    Comments

    OTHER INFORMATION

    Theoretically may decrease insulin requirements in diabetics



    See how to identify renal failure stages according to GFR calculation

    See how to diagnose irreversible renal disease

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