imidapril hydrochloride
imidapril hydrochloride.JPG

imidapril hydrochloride

CLINICAL USE

Angiotensin-converting enzyme inhibitor:Hypertension

DOSE IN NORMAL RENAL FUNCTION

2.5–20 mg once daily

PHARMACOKINETICS

  • Molecular weight                           :441.9
  • %Protein binding                           :85
  • %Excreted unchanged in urine     : 9 (as imidaprilat)
  • Volume of distribution (L/kg)       :No data
  • half-life – normal/ESRD (hrs)      :2/Increased (>24 hours as imidaprilat)

    DOSE IN RENAL IMPAIRMENT

    GFR (mL/MIN)

  • 20 to 50     : Initially 2.5 mg daily and adjust according to response
  • 10 to 20     : Initially 2.5 mg daily and adjust according to response
  • <10           : Initially 2.5 mg daily and adjust according to response

    DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES

  • CAPD                :Probably 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      :Probably dialysed. Dose as in GFR 10 to 20 mL/min

    IMPORTANT DRUG INTERACTIONS

    Potentially hazardous interactions with other drugs
  • Anaesthetics: enhanced hypotensive effect
  • Analgesics: antagonism of hypotensive effect and increased risk of renal impairment with NSAIDs; hyperkalaemia with ketorolac and other NSAIDs
  • Ciclosporin: increased risk of hyperkalaemia and nephrotoxicity
  • Diuretics: enhanced hypotensive effect; hyperkalaemia with potassium-sparing diuretics
  • Epoetin: increased risk of hyperkalaemia; antagonism of hypotensive effect
  • Lithium: reduced excretion, possibility of enhanced lithium toxicity
  • Potassium salts: increased risk of hyperkalaemia
  • Tacrolimus: increased risk of hyperkalaemia and nephrotoxicity

    ADMINISTRATION

    Reconstition

    Route

    Oral

    Rate of Administration

    Comments

    OTHER INFORMATION

    Imidapril is a prodrug, rapidly converted to the active imidaprilatHyperkalaemia and other side effects are more common in patients with impaired renal functionClose monitoring of renal function during therapy is necessary in those with renal insufficiencyRenal failure has been reported in association with ACE inhibitors with renal artery stenosis, post renal transplant or congestive heat failureHigh incidence of anaphylactoid reactions have been reported in patients dialysed with high-flux polyacrylonitrile membranes and treated concomitantly with an ACE inhibitor – combination should therefore be avoided



    See how to identify renal failure stages according to GFR calculation

    See how to diagnose irreversible renal disease

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