Last reviewed · How we verify

Plendil (FELODIPINE)

AstraZeneca · FDA-approved approved Small molecule Verified Quality 75/100

Plendil works by blocking calcium channels in blood vessel walls, causing them to relax and widen, which lowers blood pressure.

Plendil (Felodipine) is a dihydropyridine calcium channel blocker developed by AstraZeneca. It targets the voltage-dependent T-type calcium channel subunit alpha-1H, reducing blood pressure in patients with hypertensive disorders. Originally approved in 1991, Plendil is now off-patent with 13 generic manufacturers. Its half-life is 10 hours, and bioavailability is 15%. Key safety considerations include its potential to cause edema and hypotension.

At a glance

Generic nameFELODIPINE
SponsorAstraZeneca
Drug classDihydropyridine Calcium Channel Blocker [EPC]
TargetVoltage-dependent T-type calcium channel subunit alpha-1H
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved
First approval1991

Mechanism of action

Mechanism of Action. Felodipine is member of the dihydropyridine class of calcium channel antagonists (calcium channel blockers). It reversibly competes with nitrendipine and/or other calcium channel blockers for dihydropyridine binding sites, blocks voltage-dependent Ca++ currents in vascular smooth muscle and cultured rabbit atrial cells, and blocks potassium-induced contracture of the rat portal vein.In vitro studies show that the effects of felodipine on contractile processes are selective, with greater effects on vascular smooth muscle than cardiac muscle. Negative inotropic effects can be detected in vitro, but such effects have not been seen in intact animals.The effect of felodipine on blood pressure is principally consequence of dose-related decrease of peripheral vascular resistance in man, with modest reflex increase in heart rate (see Cardiovascular Effects). With the exception of mild diuretic effect seen in several animal species and man, the effects of felodipine are acc

Approved indications

Common side effects

Drug interactions

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: