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                          Ç×È÷½ºÅ¸¹Î & Ç׾˷¯Áö¾à (Antihistamines & antiallergics)
                         
                     
                    
                    
                      
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	          ÀüüÀӽŠ±â°£º°·Î ¿©·¯µî±ÞÀÌ Á¸ÀçÇÒ ¼ö ÀÖÀ¸¸ç °¡Àå À§Çèµµ°¡ ³ôÀº Á¤º¸¸¸ º¸¿©Áý´Ï´Ù. ´Ü, º¹ÇÕÁ¦ÀÇ °æ¿ì ¸ðµç º¹ÇÕÁ¦¼ººÐ¿¡ ´ëÇÑ ÀÓºÎÅõ¿©µî±ÞÀÌ Ç¥½ÃµÈ°ÍÀº Àý´ë ¾Æ´Ï¸ç Ç¥½ÃµÈ°ÍÁß¿¡ °¡Àå À§Çèµµ°¡ ³ôÀº Á¤º¸¸¸ ³ªÅ¸³³´Ï´Ù. 
	          
	         
	      
	       
	   
	  
	      
	   
	  
	    
	     FDA : Bµî±Þ 
				        
				         (loratadine; )
				        
	   
	  
	  
	  
	     
	     
	     
	     
	     
	     
	   
	 
	
	  
	      
	      
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	          »ó±â ÀÓºÎÅõ¿©¿¡ ´ëÇÑ Á¤º¸´Â Àü»êó¸® µÇ¸é¼ ÀÔ·Â ¿À·ù °¡´É¼ºÀÌ Á¸ÀçÇÕ´Ï´Ù. ¿À·ù °¡´É¼ºÀ» ÃÖ¼ÒÈÇϱâ À§ÇÏ¿© ¸¹Àº ³ë·ÂÀ» ±â¿ïÀ̰í ÀÖÀ¸³ª, ±× Á¤È®¼º¿¡ ´ëÇÏ¿© È®½ÅÀ» µå¸± ¼ö ¾ø½À´Ï´Ù. ÀÌ¿¡ ´ëÇØ ȸ»ç´Â Ã¥ÀÓÀ» ÁöÁö ¾Ê½À´Ï´Ù. 
	         
	         
	      
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      Pharmacokinetics 
      
       
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    DUR (ÀǾàǰ»ç¿ëÆò°¡) 
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    Mechanism of Action 
    
      Loratadine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸  Like other H1 -blockers, loratadine competes with free histamine for binding at H1 -receptors in the GI tract, uterus, large blood vessels, and bronchial muscle. Loratadine also has a weak affinity for acetylcholine and alpha-adrenergic receptors. 
     
   
  
   
    Pharmacology 
     
      Loratadine¿¡ ´ëÇÑ Pharmacology Á¤º¸  Loratadine, a non-sedating H1 -blocker similar in structure to cyproheptadine and azatadine, is used to treat seasonal allergic rhinitis. Unlike other H1 -blockers, loratidine does not penetrate the CNS effectively and has a low affinity for CNS H1 -receptors. 
     
   
  
   
    Metabolism 
    
      Loratadine¿¡ ´ëÇÑ Metabolism Á¤º¸  # Phase_1_Metabolizing_Enzyme:Cytochrome P450 3A4 (CYP3A4)Cytochrome P450 2C19 (CYP2C19)Cytochrome P450 2D6 (CYP2D6) 
     
   
  
   
    Protein Binding 
    
      Loratadine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸  Not Available 
     
   
  
   
    Half-life 
    
      Loratadine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸  8.4 hours 
     
   
  
   
    Absorption 
    
      Loratadine¿¡ ´ëÇÑ Absorption Á¤º¸  Rapidly absorbed following oral administration (40% bioavailability) 
     
   
  
   
    Pharmacokinetics 
    
      LoratadineÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á  
	ÀÛ¿ë¹ßÇö½Ã°£ : 1-3 ½Ã°£ À̳»
	 ÃÖ´ëÈ¿°ú ¹ßÇö½Ã°£ : 8-12 ½Ã°£
	 ÀÛ¿ëÁö¼Ó½Ã°£ : 24½Ã°£ ÀÌ»ó
	 Èí¼ö : ½Å¼ÓÈ÷ Èí¼ö
	 ´ë»ç : °£¿¡¼ Ȱ¼ºÇü ´ë»çü·Î ´ë»ç
	 ¹Ý°¨±â : 12-15 ½Ã°£
	 ¼Ò½Ç : À¯ÁóÀ¸·Îµµ »ó´ç·® ¹è¼³
  
     
   
  
   
    Biotransformation 
    
      Loratadine¿¡ ´ëÇÑ Biotransformation Á¤º¸  Hepatic 
     
   
  
   
    Toxicity 
    
      Loratadine¿¡ ´ëÇÑ Toxicity Á¤º¸  somnolence, tachycardia, and headache LD50 =mg/kg (orally in rat) 
     
   
  
   
    Drug Interactions 
    
      Loratadine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸  Nefazodone	Increased risk of cardiotoxicity 
     
   
  
   
    CYP450  Drug Interaction 
    
      [CYP450 TableÁ÷Á¢Á¶È¸]  
     
   
  
   
    Food Interaction 
    
      Loratadine¿¡ ´ëÇÑ Food Interaction Á¤º¸  Take on empty stomach: 1 hour before or 2 hours after meals. 
     
   
  
   
    Drug Target 
    
      
      [Drug Target]  
     
   
  
   
    Description 
    
      Loratadine¿¡ ´ëÇÑ Description Á¤º¸  A second-generation histamine H1 receptor antagonist used in the treatment of allergic rhinitis and urticaria. Unlike most classical antihistamines (histamine H1 antagonists) it lacks central nervous system depressing effects such as drowsiness. [PubChem] 
     
   
  
   
    Dosage Form 
    
      ÷°¡Á¦1 ¾Æ½ºÆÄŽ   (°æ±¸  Á¦¿¡ ÇÑÇÔ.)   ¡Ü 1ÀÏ Çã¿ë·®Á¦ÇÑ  
    ¾Æ½ºÆÄŽ ÇÔ·®À» WHO ±ÇÀå·®(40mg/kg/1ÀÏ)dlgkfh Á¶Á¤(°¡´ÉÇÑ ÃÖ¼Ò·® »ç¿ë)ÇÒ °Í.  
  60kg ¼ºÀÎ : 1ÀÏ Ãִ뺹¿ë·® 24g  
 ¡Ü »ç¿ë»óÀÇ ÁÖÀÇ»çÇ×  
  ¡Û °æ°í  
     ÀÌ ¾à¿¡ ÇÔÀ¯µÇ¾î ÀÖ´Â Àΰø°¨¹ÌÁ¦ ¾Æ½ºÆÄŽÀº ü³»¿¡¼ ºÐÇØµÇ¾î Æä´Ò¾Ë¶ó´ÑÀ¸·Î ´ë»çµÇ¹Ç·Î, Æä´Ò¾Ë¶ó´ÑÀÇ ¼·Ã븦 ±ÔÁ¦ÇÒ Çʿ䰡 ÀÖ´Â À¯Àü¼ºÁúȯÀÎ Æä´ÒÄÉÅæ´¢Áõ ȯÀÚ¿¡´Â Åõ¿©ÇÏÁö ¸» °Í.  
 
     
   
  
   
    Drug Category 
    
      Loratadine¿¡ ´ëÇÑ Drug_Category Á¤º¸  Anti-Allergic AgentsAntihistaminesAntipruriticsHistamine H1 Antagonists, Non-Sedating 
     
   
  
   
    Smiles String Canonical 
    
      Loratadine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸  CCOC(=O)N1CCC(CC1)=C1C2=C(CCC3=C1N=CC=C3)C=C(Cl)C=C2 
     
   
  
   
    Smiles String Isomeric 
    
      Loratadine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸  CCOC(=O)N1CC\C(CC1)=C1/C2=C(CCC3=C1N=CC=C3)C=C(Cl)C=C2 
     
   
  
   
    InChI Identifier 
    
      Loratadine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸  InChI=1/C22H23ClN2O2/c1-2-27-22(26)25-12-9-15(10-13-25)20-19-8-7-18(23)14-17(19)6-5-16-4-3-11-24-21(16)20/h3-4,7-8,11,14H,2,5-6,9-10,12-13H2,1H3 
     
   
  
   
    Chemical IUPAC Name 
    
      Loratadine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸  4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)-1-piperidinecarboxylic acid ethyl ester 
     
   
    
 
	  
	   
	
	  
       
	    
	      
	        
            
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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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