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    º¸°ü»ó ÁÖÀÇ 
    
      
    	
     
   
  
  
   
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              ½É»çÁ¤º¸ 
                             
	        
	       
	           	  
	     
	     
	  
	   
	
	  
       
	    
	      
	        
            
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    Ç׸ñ 
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    DUR (ÀǾàǰ»ç¿ëÆò°¡) 
    º´¿ë±Ý±â :
     
	     [itraconazole]  
	     
	     [itraconazole]  
	     
	 [»óÈ£ÀÛ¿ë/º´¿ë±Ý±â°Ë»ö]  										
	  ¿¬·É´ë±Ý±â :
      °í½ÃµÈ ¿¬·É±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
      
      [¿¬·É´ë±Ý±â»ó¼¼°Ë»ö]  
       
       
        
        
     
   
  
   
    Mechanism of Action 
    
      Felodipine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸  Felodipine is a calcium channel blocker. It reversibly competes with nitrendipine and/or other calcium channel blockers for dihydropyridine binding sites, blocks voltage-dependent calcium currents in vascular smooth muscle and cultured rabbit atrial cells, and blocks potassium-induced contracture of the rat portal vein. By blocking the calcium channels, felodipine inhibits the influx of extracellular calcium across the myocardial and vascular smooth muscle cell membranes and results in a decrease of peripheral vascular resistance. 
     
   
  
   
    Pharmacology 
     
      Felodipine¿¡ ´ëÇÑ Pharmacology Á¤º¸  Felodipine, a dihydropyridine calcium-channel blocker, is used alone or with an angiotensin-converting enzyme inhibitor, to treat hypertension, chronic stable angina pectoris, and Prinzmetal's variant angina. Felodipine is similar to other peripheral vasodilators. Felodipine inhibits the influx of extra cellular calcium across the myocardial and vascular smooth muscle cell membranes blocking the calcium channels. The decrease in intracellular calcium inhibits the contractile processes of the myocardial smooth muscle cells, causing dilation of the coronary and systemic arteries, increased oxygen delivery to the myocardial tissue, decreased total peripheral resistance, decreased systemic blood pressure, and decreased afterload. 
     
   
  
   
    Metabolism 
    
      Felodipine¿¡ ´ëÇÑ Metabolism Á¤º¸  # Phase_1_Metabolizing_Enzyme:Cytochrome P450 3A4 (CYP3A4) 
     
   
  
   
    Protein Binding 
    
      Felodipine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸  99% 
     
   
  
   
    Half-life 
    
      Felodipine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸  14.1 hours 
     
   
  
   
    Absorption 
    
      Felodipine¿¡ ´ëÇÑ Absorption Á¤º¸  15% 
     
   
  
   
    Pharmacokinetics 
    
      FelodipineÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á  
	ÀÛ¿ë¹ßÇö½Ã°£ : 2-5½Ã°£
	 ÀÛ¿ëÁö¼Ó½Ã°£ : 16-24½Ã°£
	 Èí¼ö : 100%  ( absolute : ÃÊȸÅë°úÈ¿°ú·Î ÀÎÇÏ¿© 20%)
	 ´Ü¹é°áÇÕ : 99% ÀÌ»ó
	 ´ë»ç : °£¿¡¼ 99% ÀÌ»ó
	 ¹Ý°¨±â : 11-16½Ã°£
	 ¼Ò½Ç : ´ë»çü·Î¼ ´¢¸¦ ÅëÇØ ¹è¼³µÈ´Ù.
  
 
	 
	
     
   
  
   
    Biotransformation 
    
      Felodipine¿¡ ´ëÇÑ Biotransformation Á¤º¸  Hepatic 
     
   
  
   
    Toxicity 
    
      Felodipine¿¡ ´ëÇÑ Toxicity Á¤º¸  Symptoms of overdose include excessive peripheral vasodilation with marked hypotension and possibly bradycardia. Oral rat LD50  is 1050 mg/kg. 
     
   
  
   
    Drug Interactions 
    
      Felodipine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸  Amobarbital	The barbiturate decreases the effect of felodipineAprobarbital	The barbiturate decreases the effect of felodipineButabarbital	The barbiturate decreases the effect of felodipineButalbital	The barbiturate decreases the effect of felodipineButethal	The barbiturate decreases the effect of felodipineCarbamazepine	Carbamazepine decreases the effect of felodipineDihydroquinidine barbiturate	The barbiturate decreases the effect of felodipineHeptabarbital	The barbiturate decreases the effect of felodipineHexobarbital	The barbiturate decreases the effect of felodipineMethohexital	The barbiturate decreases the effect of felodipineMethylphenobarbital	The barbiturate decreases the effect of felodipinePentobarbital	The barbiturate decreases the effect of felodipinePhenobarbital	The barbiturate decreases the effect of felodipinePrimidone	The barbiturate decreases the effect of felodipineQuinidine barbiturate	The barbiturate decreases the effect of felodipineSecobarbital	The barbiturate decreases the effect of felodipineTalbutal	The barbiturate decreases the effect of felodipineErythromycin	Erythromycin increases the effect of felodipineJosamycin	Erythromycin increases the effect of felodipineEthotoin	The hydantoin decreases the effect of felodipineFosphenytoin	The hydantoin decreases the effect of felodipineMephenytoin	The hydantoin decreases the effect of felodipinePhenytoin	The hydantoin decreases the effect of felodipineQuinupristin	This combination presents an increased risk of toxicityItraconazole	Itraconazole increases effect/toxicity of felodipineNelfinavir	Nelfinavir increases the effect and toxicity of felodipineOxcarbazepine	Oxcarbazepine decreases the levels of felodipineTacrolimus	Felodipine increases tacrolimus levels 
     
   
  
   
    CYP450  Drug Interaction 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] Felodipine¿¡ ´ëÇÑ P450 table SUBSTRATES  
CYP 3A4/3A5/3A7  
Macrolide antibiotics:  
clarithromycin 
erythromycin 
NOT azithromycin 
telithromycin 
Anti-arrhythmics:  
quinidine 
Benzodiazepines:  
alprazolam 
diazepam 
midazolam 
triazolam 
Immune Modulators:  
cyclosporine 
tacrolimus (FK506) 
HIV Protease Inhibitors:  
indinavir 
ritonavir 
saquinavir 
Prokinetic:  
cisapride 
Antihistamines:  
astemizole 
chlorpheniramine 
Calcium Channel Blockers:  
amlodipine 
diltiazem 
**felodipine**  
nifedipine 
nisoldipine 
nitrendipine 
verapamil 
HMG CoA Reductase Inhibitors:  
atorvastatin 
cerivastatin 
lovastatin 
NOT pravastatin 
simvastatin 
aripiprazole 
buspirone 
gleevec 
haloperidol (in part) 
methadone 
pimozide 
quinine 
NOT rosuvastatin 
sildenafil 
tamoxifen 
trazodone 
vincristine 
INHIBITORS  
CYP 3A4/3A5/3A7  
HIV Protease Inhibitors:  
indinavir 
nelfinavir 
ritonavir 
amiodarone 
NOT azithromycin 
cimetidine 
clarithromycin 
diltiazem 
erythromycin 
fluvoxamine 
grapefruit juice 
itraconazole 
ketoconazole 
mibefradil 
nefazodone 
troleandomycin 
verapamil 
INDUCERS  
CYP 3A4/3A5/3A7  
carbamazepine 
phenobarbital 
phenytoin 
rifabutin 
rifampin 
St. John's wort 
troglitazone 
 
     
   
  
   
    Food Interaction 
    
      Felodipine¿¡ ´ëÇÑ Food Interaction Á¤º¸  Take without regard to meals.Grapefruit and grapefruit juice should be avoided throughout treatment as grapefruit can significantly increase serum levels of this product. 
     
   
  
   
    Drug Target 
    
      
      [Drug Target]  
     
   
  
   
    Description 
    
      Felodipine¿¡ ´ëÇÑ Description Á¤º¸  A dihydropyridine calcium antagonist with positive inotropic effects. It lowers blood pressure by reducing peripheral vascular resistance through a highly selective action on smooth muscle in arteriolar resistance vessels. [PubChem] 
     
   
  
   
    Drug Category 
    
      Felodipine¿¡ ´ëÇÑ Drug_Category Á¤º¸  Anti-Arrhythmia AgentsAntiarrhythmic AgentsAntihypertensive AgentsCalcium Channel BlockersDihydropyridinesVasodilator Agents 
     
   
  
   
    Smiles String Canonical 
    
      Felodipine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸  CCOC(=O)C1=C(C)NC(C)=C(C1C1=C(Cl)C(Cl)=CC=C1)C(=O)OC 
     
   
  
   
    Smiles String Isomeric 
    
      Felodipine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸  CCOC(=O)C1=C(C)NC(C)=C([C@H]1C1=C(Cl)C(Cl)=CC=C1)C(=O)OC 
     
   
  
   
    InChI Identifier 
    
      Felodipine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸  InChI=1/C18H19Cl2NO4/c1-5-25-18(23)14-10(3)21-9(2)13(17(22)24-4)15(14)11-7-6-8-12(19)16(11)20/h6-8,15,21H,5H2,1-4H3 
     
   
  
   
    Chemical IUPAC Name 
    
      Felodipine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸  O3-ethyl O5-methyl 4-(2,3-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate 
     
   
    
 
	  
	   
	
	  
       
	    
	      
	        
            
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                ÃÖ±ÙÁ¤º¸¼öÁ¤ÀÏ 2025-11-03
               
              
                
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                      »ó¼¼Á¤º¸´Â ½ÄǰÀǾàǰ¾ÈÀüóÀÇ Á¦Ç°Çã°¡»çÇ×À» Åä´ë·Î ÀÛ¼ºµÇ¾úÀ¸¸ç ¿ä¾àÁ¤º¸´Â »ó¼¼Á¤º¸ ¹× ±âŸ¹®ÇåÀ» ±â¹ÝÀ¸·Î µå·°ÀÎÆ÷¿¡¼ ÆíÁýÇÑ ³»¿ëÀÔ´Ï´Ù. Á¦Ç°Çã°¡»çÇ×ÀÇ ¸ñÂ÷¿Í ´Ù¼Ò »óÀÌÇÒ ¼ö ÀÖ½À´Ï´Ù.  
                    
                  
 
               
      
      
                
                    
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                      µå·°ÀÎÆ÷ ÀǾàÇмúÁ¤º¸´Â ½ÄǰÀǾàǰ¾ÈÀüóÀÇ Á¦Ç°Çã°¡»çÇ×, Çмú¹®Çå, Á¦¾àȸ»ç Á¦°øÁ¤º¸ µîÀ» ±Ù°Å·Î ÀÛ¼ºµÈ Âü°í Á¤º¸ÀÔ´Ï´Ù. 
                          Á¤º¸ÀÇ Á¤È®¼ºÀ» À§ÇØ ³ë·ÂÇϰí ÀÖÀ¸³ª ÆíÁý»óÀÇ ¿À·ù, Çã°¡»çÇ× º¯°æ, Ãß°¡ÀûÀÎ Çмú¿¬±¸ ¶Ç´Â Àӻ󿬱¸ ¹ßÇ¥ µîÀ¸·Î ÀÎÇØ ¹ß»ýÇÏ´Â ¹®Á¦¿¡ ´ëÇØ µå·°ÀÎÆ÷´Â 
                          Ã¥ÀÓÀ» ÁöÁö ¾Ê½À´Ï´Ù. ÀÚ¼¼ÇÑ ³»¿ëÀº ¡°Ã¥ÀÓÀÇ ÇÑ°è ¹× ¹ýÀû°íÁö¡± ¸¦ ÂüÁ¶ÇØ ÁֽʽÿÀ.
                            ¹Ýµå½Ã Á¦Á¶¡¤¼öÀÔ»ç, ÆÇ¸Å»ç, ÀÇ»ç, ¾à»ç¿¡°Ô ÃÖÁ¾ÀûÀ¸·Î È®ÀÎÇϽñ⠹ٶø´Ï´Ù. 
                          ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
 
                    
                  
 
               
  
  
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  The database contains the following fields:
The generic name of each chemical
For module A10 (liver enzyme composite module):
Overall activity category for each compound (A for active, M for marginally active, or I for inactive) based on the number of active and marginally active scores for each compound at the five individual endpoints (see research article for full description of method)
Number of endpoints at which each compound is marginally active (M)
Number of endpoints at which each compound is active (A)
For modules A11 to A15 (alkaline phosphatase increased, SGOT increased, SGPT increased, LDH increased, and GGT increased, respectively):
Overall activity category for each compound (A for active, M for marginally active, or I for inactive) based on the RI and ADR values (see the research article for full description of method)
Number of ADR reports for each compound, given as <4 or ¡Ã4
Reporting Index value for each compound, except where no shipping units were available (NSU)
Group 1 comprises of compounds for which ADR data were available for the first five years of marketing, so when no ADR reports were listed during this period the compounds were evaluated as inactive. Group 2 comprises of compounds for which a 'steady state' period of ADR data were available (1992-1996). In cases where no ADR reports were filed during this period, the compounds were scored as 'NA' (data not available) since they may have had one or more ADR reports during their first five years of marketing which should not be negated by a lack of ADR reports during the steady-state period.
FELODIPINE [GGT Increase] [Composite Activity] (Score)   I  (Marginal)   0 (Active)   0 [Alkaline Phosphatase Increase] (Activity Score)   I  (Number of Rpts)   <4 (Index value)   0.6 [SGOT Increase] (Activity Score)   I  (Number of Rpts)   <4 (Index value)   0.3 [SGPT Increase] (Activity Score)   I  (Number of Rpts)   <4 (Index value)   0.3 [LDH Increase] (Activity Score)   I  (Number of Rpts)   <4 (Index value)   0.3 [GGT Increase] (Activity Score)   I  (Number of Rpts)   <4 (Index value)   0.3 
 
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