Drug class
Calcium Channel Blockers
Calcium channel blockers are a recognized class of cardiovascular medications that inhibit the transmembrane influx of calcium ions into cardiac muscle and vascular smooth muscle through voltage-gated L-type calcium channels. Read more about Calcium Channel Blockers
344 drugs in this class 144 manufacturers
Drugs in Calcium Channel Blockers
CARDAMYST (etripamil)
DILTIAZEM HCL
NICARDIPINE HCL
VERAPAMIL HCL
NICARDIPINE HCL
AMLODIPINE BESYLATE-BENAZEPRIL (amlodipine besylate/benazepril HCl)
DILTIAZEM 24HR ER (CD) (diltiazem HCl)
SDAMLO (amlodipine besylate)
Calcium channel blockers are a recognized class of cardiovascular medications that inhibit the transmembrane influx of calcium ions into cardiac muscle and vascular smooth muscle through voltage-gated L-type calcium channels.
By decreasing intracellular calcium availability, they promote vascular smooth muscle relaxation and arterial vasodilation, while non-dihydropyridine subclasses also depress sinoatrial node automaticity and delay atrioventricular conduction.
Therapeutically, this pharmacologic class is widely indicated for the management of hypertension, chronic stable and vasospastic angina pectoris, and certain supraventricular arrhythmias.
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fda.gov
Calcium channel blockers are a recognized class of cardiovascular medications that inhibit the transmembrane influx of calcium ions into cardiac muscle and vascular smooth muscle through voltage-gated L-type calcium channels By decreasing intracellular calcium availability, they promote vascular smooth muscle relaxation and arterial vasodilation, while non-dihydropyridine subclasses also depress sinoatrial node automaticity and delay atrioventricular conduction
-
nih.gov
Calcium channel blockers are a recognized class of cardiovascular medications that inhibit the transmembrane influx of calcium ions into cardiac muscle and vascular smooth muscle through voltage-gated L-type calcium channels By decreasing intracellular calcium availability, they promote vascular smooth muscle relaxation and arterial vasodilation, while non-dihydropyridine subclasses also depress sinoatrial node automaticity and delay atrioventricular conduction
-
fda.gov
By decreasing intracellular calcium availability, they promote vascular smooth muscle relaxation and arterial vasodilation, while non-dihydropyridine subclasses also depress sinoatrial node automaticity and delay atrioventricular conduction Therapeutically, this pharmacologic class is widely indicated for the management of hypertension, chronic stable and vasospastic angina pectoris, and certain supraventricular arrhythmias
-
fda.gov
Therapeutically, this pharmacologic class is widely indicated for the management of hypertension, chronic stable and vasospastic angina pectoris, and certain supraventricular arrhythmias
-
nih.gov
Therapeutically, this pharmacologic class is widely indicated for the management of hypertension, chronic stable and vasospastic angina pectoris, and certain supraventricular arrhythmias
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