LEVEL 4 G04BD10

Δραστικές

Φάρμακα

  • DRUGBANK - Darifenacin
  • indication:

    For the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency and frequency.

  • pharmacology:

  • mechanism:

    Darifenacin selectively antagonizes the muscarinic M3 receptor. M3 receptors are involved in contraction of human bladder and gastrointestinal smooth muscle, saliva production, and iris sphincter function.

  • toxicity:

    Overdosage can potentially result in severe central anticholinergic effects.

  • absorprion:

    The mean oral bioavailability at steady state is estimated to be 15% and 19% for 7.5 mg and 15 mg tablets, respectively.

  • halflife:

    The elimination half-life of darifenacin following chronic dosing is approximately 13-19 hours.

  • roouteelimination:

  • volumedistribution:

    * 163 L

  • clearance:

    * 40 L/h [extensive metabolizers] * 32 L/h [poor metabolizers]