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                    ´í¹ö¸®¿°»êÇÁ·ÎÄ«Àξƹ̵åݼ¿  [Procainamide HCl]  
                    
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                     Àü¹®ÀǾàǰ | ºñ±Þ¿©  
                        
                    	
                    
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        [E01510371]  
	    
	    
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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. 
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	      FDA : Cµî±Þ 
				        
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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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	 °í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
	 
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    | Mechanism of Action | 
    
       Procainamide¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Procainamide is sodium channel blocker. It stabilizes the neuronal membrane by inhibiting the ionic fluxes required for the initiation and conduction of impulses thereby effecting local anesthetic action. 
     | 
   
  
   
    | Pharmacology | 
     
       Procainamide¿¡ ´ëÇÑ Pharmacology Á¤º¸ Procainamide is an agent indicated for production of local or regional anesthesia and in the treatment of ventricular tachycardia occurring during cardiac manipulation, such as surgery or catheterization, or which may occur during acute myocardial infarction, digitalis toxicity, or other cardiac diseases. The mode of action of the antiarrhythmic effect of Procainamide appears to be similar to that of procaine and quinidine. Ventricular excitability is depressed and the stimulation threshold of the ventricle is increased during diastole. The sinoatrial node is, however, unaffected. 
     | 
   
  
   
    | Protein Binding | 
    
       Procainamide¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 15 to 20% 
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    | Half-life | 
    
       Procainamide¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ ~2.5-4.5 hours 
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    | Absorption | 
    
       Procainamide¿¡ ´ëÇÑ Absorption Á¤º¸ 75 to 95% 
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    | Pharmacokinetics | 
    
       Procainamide HClÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á 
 
- ÀÛ¿ë¹ßÇö½Ã°£ : ±ÙÀ°ÁÖ»ç : 10-30ºÐ
 
 - »ýü³»ÀÌ¿ë·ü : °æ±¸ : 75-95%
 
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-    ¼Ò¾Æ : 2.2 L/kg  
 
 -    ¼ºÀÎ 2 L/kg 
 
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 - ´Ü¹é°áÇÕ : 15-20%
 
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 - ¹Ý°¨±â : 
 
-    Procainamide (°£ ¾Æ¼¼Æ¿È´É·Â, À¯ÀüÇü, ½ÉÀå±â´É, ½ÅÀå±â´É¿¡ ÀÇÁ¸Àû) :
 
	- ¼Ò¾Æ : 1.7 ½Ã°£
 
	 - ¼ºÀÎ : 2.5-4.7 ½Ã°£
 
	 - ½ÅÀå±â´ÉÀÌ ¾ø´Â »óÅ (anephric) : 11½Ã°£
   
 -    NAPA (½ÅÀå±â´É¿¡ ÀÇÁ¸Àû) :
      | 
   
  
   
    | Biotransformation | 
    
       Procainamide¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic 
     | 
   
  
   
    | Toxicity | 
    
       Procainamide¿¡ ´ëÇÑ Toxicity Á¤º¸ LD50=95 mg/kg (rat, IV); LD50=312 mg/kg (mouse, oral); LD50=103 mg/kg (mouse, IV); LD50=250 mg/kg (rabbit, IV) 
     | 
   
  
   
    | Drug Interactions | 
    
       Procainamide¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Amiodarone	Amiodarone increases serum levels and toxicity of procainamideCimetidine	The histamine H2-receptor antagonist increases the effect of procainamideRanitidine	The histamine H2-receptor antagonist increases the effect of procainamideCiprofloxacin	The quinolone increases the effect of procainamideLevofloxacin	The quinolone increases the effect of procainamideOfloxacin	The quinolone increases the effect of procainamideDihydroquinidine barbiturate	Quinidine increases the effect of procainamideQuinidine	Quinidine increases the effect of procainamideQuinidine barbiturate	Quinidine increases the effect of procainamideRanolazine	Possible additive effect on QT prolongationRivastigmine	Possible antagonism of actionDonepezil	Possible antagonism of actionGalantamine	Possible antagonism of actionCisapride	Increased risk of cardiotoxicity and arrhythmiasMesoridazine	Increased risk of cardiotoxicity and arrhythmiasThioridazine	Increased risk of cardiotoxicity and arrhythmiasTerfenadine	Increased risk of cardiotoxicity and arrhythmiasZiprasidone	Increased risk of cardiotoxicity and arrhythmiasVardenafil	Increased risk of cardiotoxicity and arrhythmiasTrimethoprim	Trimethoprim increases serum levels of procainamide 
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    CYP450  Drug Interaction | 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] 
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    | Description | 
    
       Procainamide¿¡ ´ëÇÑ Description Á¤º¸ A derivative of procaine with less CNS action. [PubChem] 
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    | Dosage Form | 
    
       Procainamide¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Capsule	OralSolution	IntramuscularTablet, extended release	Oral 
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    | Drug Category | 
    
       Procainamide¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Arrhythmia AgentsAntiarrhythmic Agents 
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    | Smiles String Canonical | 
    
       Procainamide¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CCN(CC)CCNC(=O)C1=CC=C(N)C=C1 
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    | Smiles String Isomeric | 
    
       Procainamide¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CCN(CC)CCNC(=O)C1=CC=C(N)C=C1 
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    | InChI Identifier | 
    
       Procainamide¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C13H21N3O/c1-3-16(4-2)10-9-15-13(17)11-5-7-12(14)8-6-11/h5-8H,3-4,9-10,14H2,1-2H3,(H,15,17)/f/h15H 
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    | Chemical IUPAC Name | 
    
       Procainamide¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 4-amino-N-(2-diethylaminoethyl)benzamide 
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    | Drug-Induced Toxicity Related Proteins | 
    
      PROCAINAMIDE ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸ Replated Protein:N-acetyltransferase Drug:Procainamide Toxicity:Drug-induced lupus.  [¹Ù·Î°¡±â] Replated Protein:CYP2D6 Drug:Procainamide Toxicity:idiosyncratic hepatotoxicity.  [¹Ù·Î°¡±â] 
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