Open Access Articles- Top Results for Felodipine


File:(±)-Felodipine formulae V.1.svg
Systematic (IUPAC) name
(RS)-3-ethyl 5-methyl 4-(2,3-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
Clinical data
Trade names Plendil
AHFS/ monograph
MedlinePlus a692016
  • US: C (Risk not ruled out)
  • (Prescription only)
Pharmacokinetic data
Bioavailability 15% [1]
Metabolism Hepatic
Half-life 25hours [2]
Excretion Renal
72509-76-3 7pxY
PubChem CID 3333
IUPHAR ligand 4190
DrugBank DB01023 7pxY
ChemSpider 3216 7pxY
UNII OL961R6O2C 7pxY
KEGG D00319 7pxY
ChEBI CHEBI:585948 7pxY
Chemical data
Formula C18H19Cl2NO4
384.259 g/mol
 14pxY (what is this?)  (verify)

Felodipine is a calcium channel blocker (calcium antagonist), a drug used to control hypertension (high blood pressure). It is marketed under the brand name Plendil by AstraZeneca and Renedil by Sanofi-Aventis. The formulation patent for the substance expired in 2007.

AstraZeneca dropped Plendil from its support and AZ&Me free Rx access program in October 2008.


Studies dating back to 1989 have suggested that felodipine in combination with grapefruit juice can cause toxic effects. Oral administration of felodipine is first metabolized in the gastrointestinal tract and liver by the enzyme CYP3A4. Grapefruit juice contains bergamottin which is found to have an inhibiting effect over this enzyme and as a result the bioavailability of the drug increases, raising the risk for abnormal side effects.[3]

Contraindications and cautions

Contraindicated with allergy to felodipine or other calcium channel blockers, sick sinus syndrome, heart block (second and third degree), lactation. Use cautiously with pregnancy, impaired hepatic function.



Berntsson, P. B.; Carlsson, A. I.; Gaarder, J. O.; Ljung, B. R.; 1981, U.S. Patent 4,264,611.


  1. ^ AstraZeneca MI Department, 16 April 2010.
  2. ^,+Plendil+5mg+and+Plendil+10mg/
  3. ^ Jawad Kiani, Sardar Z Imam (October 30, 2007). "Medicinal importance of grapefruit juice and its interaction with various drugs". Nutr J. 6 (33): 33. PMC 2147024. PMID 17971226. doi:10.1186/1475-2891-6-33. Retrieved 2008-04-09. .

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