Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Felodipine
Drug ID BADD_D00872
Description Felodipine is a long-acting 1,4-dihydropyridine calcium channel blocker (CCB)b. It acts primarily on vascular smooth muscle cells by stabilizing voltage-gated L-type calcium channels in their inactive conformation. By inhibiting the influx of calcium in smooth muscle cells, felodipine prevents calcium-dependent myocyte contraction and vasoconstriction. Felodipine is the most potent CCB in use and is unique in that it exhibits fluorescent activity. In addition to binding to L-type calcium channels, felodipine binds to a number of calcium-binding proteins, exhibits competitive antagonism of the mineralcorticoid receptor, inhibits the activity of calmodulin-dependent cyclic nucleotide phosphodiesterase, and blocks calcium influx through voltage-gated T-type calcium channels. Felodipine is used to treat mild to moderate essential hypertension.
Indications and Usage For the treatment of mild to moderate essential hypertension.
Marketing Status Prescription; Discontinued
ATC Code C08CA02
DrugBank ID DB01023
KEGG ID D00319
MeSH ID D015736
PubChem ID 3333
TTD Drug ID D0WN0U
NDC Product Code 53489-369; 63629-2017; 63629-2194; 71205-922; 53296-0041; 23155-048; 51407-088; 65862-674; 50090-5870; 13668-132; 63629-2193; 63629-2191; 66406-0275; 23155-050; 65862-673; 61442-432; 61442-431; 63629-2018; 71335-1486; 50090-2421; 64679-412; 71335-1318; 65862-399; 51407-087; 57237-109; 63629-2192; 66406-0276; 65035-105; 53104-7519; 0603-3582; 0603-3583; 13668-133; 14799-2007; 63629-2016; 53489-368; 23155-049; 57237-110; 63629-2196; 64679-414; 58657-685; 66406-0277; 61442-433; 13668-134; 57237-108; 65862-675; 46708-926; 68462-233; 63629-2195; 58657-687; 51407-089; 68462-235; 53489-370; 68462-234; 71205-921; 71205-920; 58657-686; 64679-411; 0603-3581
Synonyms Felodipine | Felo Biochemie | Felo-Puren | Felo Puren | Felobeta | Felocor | Felodipin 1A Pharma | Felodipin AbZ | Felodipin AL | Felodipin AZU | Felodipin Dura | Felodipin Heumann | Heumann, Felodipin | Felodipin Stada | Felodipin Von Ct | Von Ct, Felodipin | Felodipin-Ratiopharm | Felodipin Ratiopharm | Felodur | Felogamma | Fensel | H 154-82 | H 154 82 | H 15482 | Perfudal | Plendil | Flodil | Modip | Renedil | Munobal | Agon
Chemical Information
Molecular Formula C18H19Cl2NO4
CAS Registry Number 72509-76-3
SMILES CCOC(=O)C1=C(NC(=C(C1C2=C(C(=CC=C2)Cl)Cl)C(=O)OC)C)C
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Influenza22.07.02.001; 11.05.03.001--Not Available
Influenza like illness08.01.03.010--
Insomnia19.02.01.002; 17.15.03.002--
Intentional self-injury19.12.01.002; 12.01.08.0360.002398%Not Available
Irritability19.04.02.013; 08.01.03.011--
Joint swelling15.01.02.004--Not Available
Libido decreased21.03.02.005; 19.08.03.001--
Lichen planus23.03.08.0010.001599%Not Available
Lip swelling23.04.01.007; 10.01.05.005; 07.05.04.0050.001599%Not Available
Lipase increased13.05.01.0030.001599%
Loss of consciousness17.02.04.004--Not Available
Loss of libido19.08.03.003--Not Available
Micturition urgency20.02.02.006--
Muscle spasms15.05.03.004--
Myalgia15.05.02.001--
Myocardial infarction24.04.04.009; 02.02.02.007--
Nasopharyngitis22.07.03.002; 11.01.13.002--Not Available
Nausea07.01.07.0010.003198%
Nervousness19.06.02.003--Not Available
Oedema08.01.07.006; 14.05.06.0100.003198%Not Available
Oedema mouth23.04.01.008; 10.01.05.006; 07.05.04.0010.001599%Not Available
Oedema peripheral08.01.07.007; 02.05.04.007; 14.05.06.0110.003997%
Orthostatic hypotension24.06.03.004; 17.05.01.0200.001599%Not Available
Pain in extremity15.03.04.010--
Palpitations02.01.02.0030.003997%
Paraesthesia17.02.06.005--
Pharyngitis11.01.13.003; 07.05.07.004; 22.07.03.004--
Photosensitivity reaction23.03.09.003--
Pollakiuria20.02.02.007--
Polyuria20.02.03.002--Not Available
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