Amlodipine

CLINICAL USE


Calcium-channel blocker:

  • Hypertension
  • Angina prophylaxis

    DOSE IN NORMAL RENAL FUNCTION


    5–10 mg daily

    PHARMACOKINETICS


  • Molecular weight &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp :
    567.1 (as besilate)
  • %Protein binding &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp :
    >95
  • %Excreted unchanged in urine &nbsp &nbsp :
  • <10 &nbsp &nbsp &nbsp &nbsp &nbsp :
  • Volume of distribution (L/kg) &nbsp &nbsp &nbsp :
    20
  • half-life – normal/ESRD (hrs)&nbsp &nbsp &nbsp :
    35–50/50

    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:
    Not dialysed. Dose as in normal renal function

  • HD &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp &nbsp :
    Not dialysed. Dose as in normal renal function
  • HDF/high flux &nbsp :
    Unlikely to be dialysed. Dose as in
    normal renal function
  • CAV/VVHD &nbsp &nbsp &nbsp:
    Not dialysed. Dose as in normal renal function

    IMPORTANT DRUG INTERACTIONS


    Potentially hazardous interactions with other drugs

  • Anaesthetics: enhanced hypotensive effect
  • Antihypertensives: enhanced hypotensive

    effect; increased risk of first dose
    hypotensive effect of post-synaptic alpha-
    blockers

  • Antivirals: concentration possibly

    increased by ritonavir
    Theophylline: possibly increased

    theophylline concentration

    ADMINISTRATION


    Reconstition



    Route


    Oral

    Rate of Administration



    Comments



    OTHER INFORMATION


    Amlodipine is extensively metabolised to

    inactive metabolites