Acipimox
Acipimox.JPG

Acipimox

CLINICAL USE

Hyperlipidaemia

DOSE IN NORMAL RENAL FUNCTION

250 mg 2 or 3 times daily

PHARMACOKINETICS

  • Molecular weight                           : 154.1
  • %Protein binding                           : 0
  • %Excreted unchanged in urine     : 86–90
  • Volume of distribution (L/kg)       : 0.3–0.4
  • half-life – normal/ESRD (hrs)      : 2/Increased

    DOSE IN RENAL IMPAIRMENT

    GFR (mL/MIN)

    40–80 250 mg daily 20–40 250 mg alternate days. <20 See ‘Other Information’

    DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES

  • CAPD                : Likely dialysability. Dose as in GFR<20 mL/min
  • HD                     : Dialysed. Dose as in GFR<20 mL/min
  • HDF/high flux   : Dialysed. Dose as in GFR<20 mL/min
  • CAV/VVHD      : Dialysed. Dose as in GFR=20–40 mL/min

    IMPORTANT DRUG INTERACTIONS

    Potentially hazardous interactions with other drugs
  • None known

    ADMINISTRATION

    Reconstition

    Route

    Oral

    Rate of Administration

    Comments

    Take with or after meals

    OTHER INFORMATION

  • Females are twice as likely as males to suffer from side effects, e.g. flushing, pruritus and skin rashes
  • Doses up to 1200 mg have been given safely for long periods After a 5 hour dialysis 70% of the drug had been removed
  • Dollery advises the doses given in the table, down to 20 mL/minute, but nothing after that. Micromedex gives the following recommendations: GFR: 30–60 mL/min 150 mg twice daily GFR: 10–30 mL/min 150 mg once daily GFR:
  • <10           : mL/min 150 mg alternate days



    See how to identify renal failure stages according to GFR calculation

    See how to diagnose irreversible renal disease

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