Mibefradil represents a drew class of selective T-type channel calcium
channel blockers (CCBs) approved for use in the treatment of hyperten
sion and, stable angina, Although mibefradil acts principally on arter
ial smooth muscle to induce vasodilation, it does not cause reflex tac
hycardia or increased sympathetic activity, It causes a decrease in he
art rate without negative inotropic effects. In clinical trials, mibef
radil was at least as effective as other available CCBs (nifedipine GI
TS, amlodipine, diltiazem CD) for the treatment of hypertension and ch
ronic stable angina, While the incidence of adverse effects with mibef
radil is similar to that with other CCBs, mibefradil may cause less pe
ripheral edema and more bradycardia and AV block than certain CCBs (eg
, dihydropyridines). Mibefradil can inhibit the P450 3A4 and 2D6 isoen
zymes; thus, concurrent administration of hepatically eliminated drugs
, such as terfenadine, astemizole, and, cisapride, should be avoided.