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      Piroxicam¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸  The antiinflammatory effect of Piroxicam may result from the reversible inhibition of cyclooxygenase, causing the peripheral inhibition of prostaglandin synthesis. The prostaglandins are produced by an enzyme called Cox-1. Piroxicam blocks the Cox-1 enzyme, resulting into the disruption of production of prostaglandins. Piroxicam also inhibits the migration of leukocytes into sites of inflammation and prevents the formation of thromboxane A2, an aggregating agent, by the platelets. 
     
   
  
   
    Pharmacology 
     
      Piroxicam¿¡ ´ëÇÑ Pharmacology Á¤º¸  Piroxicam is in a class of drugs called nonsteroidal anti-inflammatory drugs (NSAIDs). Piroxicam works by reducing hormones that cause inflammation and pain in the body. Piroxicam is used to reduce the pain, inflammation, and stiffness caused by rheumatoid arthritis and osteoarthritis. 
     
   
  
   
    Metabolism 
    
      Piroxicam¿¡ ´ëÇÑ Metabolism Á¤º¸  # Phase_1_Metabolizing_Enzyme:Not Available 
     
   
  
   
    Half-life 
    
      Piroxicam¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸  30 to 86 hours 
     
   
  
   
    Absorption 
    
      Piroxicam¿¡ ´ëÇÑ Absorption Á¤º¸  Well absorbed following oral administration. 
     
   
  
   
    Pharmacokinetics 
    
      PiroxicamÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á  
ÁøÅëÈ¿°ú ¹ßÇö½Ã°£ : °æ±¸ : 1½Ã°£ À̳»
 ÃÖ´ëÈ¿°ú ¹ßÇö½Ã°£ : 3-5 ½Ã°£
 ´Ü¹é°áÇÕ : 99%
 ´ë»ç : °£´ë»ç
 ¹Ý°¨±â : 45-50 ½Ã°£
 ¼Ò½Ç : ¹Ìº¯Èü(5%) ¹× ´ë»çü·Î¼ ÁÖ·Î ´¢¸¦ ÅëÇØ, ¼Ò·®Àº ´ëº¯À¸·Î ¹è¼³µÊ
  
     
   
  
   
    Biotransformation 
    
      Piroxicam¿¡ ´ëÇÑ Biotransformation Á¤º¸  Renal 
     
   
  
   
    Toxicity 
    
      Piroxicam¿¡ ´ëÇÑ Toxicity Á¤º¸  Symptoms of overdose include drowsiness, nausea, stomach pain, and/or vomiting. 
     
   
  
   
    Drug Interactions 
    
      Piroxicam¿¡ ´ëÇÑ Drug_Interactions Á¤º¸  Acebutolol	Risk of inhibition of renal prostaglandinsAtenolol	Risk of inhibition of renal prostaglandinsBetaxolol	Risk of inhibition of renal prostaglandinsBevantolol	Risk of inhibition of renal prostaglandinsBisoprolol	Risk of inhibition of renal prostaglandinsCarteolol	Risk of inhibition of renal prostaglandinsCarvedilol	Risk of inhibition of renal prostaglandinsEsmolol	Risk of inhibition of renal prostaglandinsLabetalol	Risk of inhibition of renal prostaglandinsMetoprolol	Risk of inhibition of renal prostaglandinsNadolol	Risk of inhibition of renal prostaglandinsOxprenolol	Risk of inhibition of renal prostaglandinsPenbutolol	Risk of inhibition of renal prostaglandinsPindolol	Risk of inhibition of renal prostaglandinsPractolol	Risk of inhibition of renal prostaglandinsPropranolol	Risk of inhibition of renal prostaglandinsSotalol	Risk of inhibition of renal prostaglandinsTimolol	Risk of inhibition of renal prostaglandinsRitonavir	Ritonavir increases the toxicity of piroxicamWarfarin	The NSAID increases the anticoagulant effectAcenocoumarol	The NSAID increases the anticoagulant effectDicumarol	The NSAID increases the anticoagulant effectAnisindione	The NSAID increases the anticoagulant effectLithium	The NSAID increases serum levels of lithiumMethotrexate	The NSAID increases the effect and toxicity of methotrexateCyclosporine	Monitor for nephrotoxicityAlendronate	Increased risk of gastric toxicity 
     
   
  
   
    CYP450  Drug Interaction 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] Piroxicam¿¡ ´ëÇÑ P450 table SUBSTRATES  
CYP 2C9  
NSAIDs:  
diclofenac 
ibuprofen 
**piroxicam**  
Oral Hypoglycemic Agents:  
tolbutamide 
glipizide 
Angiotensin II Blockers:  
NOT candesartan 
irbesartan 
losartan 
NOT valsartan 
celecoxib 
fluvastatin naproxen 
phenytoin 
sulfamethoxazole 
tamoxifen 
tolbutamide 
torsemide 
warfarin 
INHIBITORS  
CYP 2C9  
amiodarone 
fluconazole 
isoniazid 
INDUCERS  
CYP 2C9  
rifampin 
secobarbital 
 
     
   
  
   
    Food Interaction 
    
      Piroxicam¿¡ ´ëÇÑ Food Interaction Á¤º¸  Take with food. Avoid alcohol. 
     
   
  
   
    Drug Target 
    
      
      [Drug Target]  
     
   
  
   
    Description 
    
      Piroxicam¿¡ ´ëÇÑ Description Á¤º¸  A cyclooxygenase inhibiting, non-steroidal anti-inflammatory agent (NSAID) that is well established in treating rheumatoid arthritis and osteoarthritis and used for musculoskeletal disorders, dysmenorrhea, and postoperative pain. Its long half-life enables it to be administered once daily. [PubChem] 
     
   
  
   
    Dosage Form 
    
      ÷°¡Á¦1 º¥Áú¾ËÄÚ¿Ã   (ÁÖ»ç  Á¦¿¡ ÇÑÇÔ.)    ¡Û °æ°í  
     º¥Áú¾ËÄÚ¿ÃÀº ¹Ì¼÷¾Æ¿¡¼ Ä¡¸íÀûÀÎ °¡»Û È£ÈíÁõ»ó°ú ¿¬°üÀÌ ÀÖ´Â °ÍÀ¸·Î º¸°íµÇ¾ú´Ù.  
  ¡Û ´ÙÀ½ ȯÀÚ¿¡´Â Åõ¿©ÇÏÁö ¸» °Í.  
     ½Å»ý¾Æ, ¹Ì¼÷¾Æ(º¥Áú¾ËÄÚ¿ÃÀ» ÇÔÀ¯Çϰí ÀÖ´Ù.)  
 
     
   
  
   
    Drug Category 
    
      Piroxicam¿¡ ´ëÇÑ Drug_Category Á¤º¸  Anti-Inflammatory Agents, Non-SteroidalCyclooxygenase Inhibitors 
     
   
  
   
    Smiles String Canonical 
    
      Piroxicam¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸  CN1S(=O)(=O)C2=CC=CC=C2C(=O)C1=C(O)NC1=CC=CC=N1 
     
   
  
   
    Smiles String Isomeric 
    
      Piroxicam¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸  CN1S(=O)(=O)C2=CC=CC=C2C(=O)\C1=C(/O)NC1=CC=CC=N1 
     
   
  
   
    InChI Identifier 
    
      Piroxicam¿¡ ´ëÇÑ InChI_Identifier Á¤º¸  InChI=1/C15H13N3O4S/c1-18-13(15(20)17-12-8-4-5-9-16-12)14(19)10-6-2-3-7-11(10)23(18,21)22/h2-9,20H,1H3,(H,16,17)/b15-13+/f/h17H 
     
   
  
   
    Chemical IUPAC Name 
    
      Piroxicam¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸  (3E)-3-[hydroxy-(pyridin-2-ylamino)methylidene]-2-methyl-1,1-dioxobenzo[e]thiazin-4-one 
     
   
  
   
    Drug-Induced Toxicity Related Proteins 
    
      PIROXICAM   ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸Replated Protein  :Glycogen synthaseDrug  :piroxicam Toxicity  :impairment into glycogen metabolism. liver unable to maintain glucose homeostasis. [¹Ù·Î°¡±â]  
     
   
    
 
	  
	   
	
	  
       
	    
	      
	        
            
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