FOCUS ON MIBEFRADIL - A NOVEL SELECTIVE T-TYPE CALCIUM-CHANNEL BLOCKER

Authors
Citation
A. Dunn et Mss. Chow, FOCUS ON MIBEFRADIL - A NOVEL SELECTIVE T-TYPE CALCIUM-CHANNEL BLOCKER, Formulary, 32(11), 1997, pp. 1115
Citations number
20
Categorie Soggetti
Pharmacology & Pharmacy
Journal title
ISSN journal
1082801X
Volume
32
Issue
11
Year of publication
1997
Database
ISI
SICI code
1082-801X(1997)32:11<1115:FOM-AN>2.0.ZU;2-E
Abstract
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.