Topiramate
Topiramate.JPG

CLINICAL USE

Anti-epileptic agent Prophylactic treatment of migraine

DOSE IN NORMAL RENAL FUNCTION

Epilepsy: 50–400 mg twice daily Migraine: Initially, 25 mg at night. Maintenance, 25–50 mg twice daily

PHARMACOKINETICS

  • Molecular weight                           : 339.4
  • %Protein binding                           : 9–17
  • %Excreted unchanged in urine     : 70
  • Volume of distribution (L/kg)       : 0.55–0.8
  • half-life – normal/ESRD (hrs)      : 20–30/48–60 (12–15 hours if used with another enzyme-inducing anti-epileptic drug)

    DOSE IN RENAL IMPAIRMENT

    GFR (mL/MIN)

  • 20 to 50     : Migraine/epilepsy: Dose as in normal renal function
  • 10 to 20     : Migraine: Dose as in normal renal function Epilepsy: 50% of normal dose and increase according to response
  • <10           : Migraine: Dose as in normal renal function Epilepsy: 25–50% of normal dose and increase according to response

    DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES

  • CAPD                : Unknown dialysability. Dose as for GFR <10 mL/min
  • HD                     : Dialysed. Dose as for GFR <10 mL/min
  • HDF/high flux   : Dialysed. Dose as for GFR <10 mL/min
  • CAV/VVHD      : Unknown dialysability. Dose as for GFR 10 to 20 mL/min

    IMPORTANT DRUG INTERACTIONS

    Potentially hazardous interactions with other drugs
  • Antidepressants: antagonism of anticonvulsant effect
  • Anti-epileptics: concentration reduced by phenytoin and carbamazepine; increases phenytoin concentration
  • Antimalarials: mefloquine antagonises anticonvulsant effect; chloroquine and hydroxychloroquine occasionally reduces convulsive threshold Oestrogens and progestogens: reduced contraceptive effect

    ADMINISTRATION

    Reconstition

    Route

    Oral

    Rate of Administration

    Comments

    OTHER INFORMATION

    Patients with moderate to severe renal impairment may take 10–15 days to reach steady state, compared to 4–8 days in patients with normal renal function A higher frequency of renal stones has been noted in topiramate treated patients, although the risk is not related to dose or duration of therapy. Adequate hydration is recommended to reduce this risk .



    See how to identify renal failure stages according to GFR calculation

    See how to diagnose irreversible renal disease

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