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      1) ½Äµµ¿¡ Á¤·ùÇÏ¿© ºØ±«µÇ¸é µå¹°°Ô ½Äµµ ¼Õ»óÀ»ÀÏÀ¸Å³ ¼ö ÀÖÀ¸¹Ç·Î ´Ù·®ÀÇ ¹°°ú ÇÔ²² º¹¿ëÇϸç, Ãëħ Á÷ÀüÀÇ º¹¿ë µî¿¡´Â ƯÈ÷ ÁÖÀÇÇÑ´Ù.(ݼ¿,Á¤Á¦¿¡ ÇÑÇÔ)  
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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 : Dµî±Þ 
				        
				         (doxycycline; )
				        
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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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      [º´¿ë±Ý±â ¹× ¿¬·É´ë±Ý±â ±Ù°ÅÁ¶È¸]
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    | º¸°ü»ó ÁÖÀÇ | 
    
      
    	
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    | Á¶Á¦½Ã ÁÖÀÇ | 
    
      
    	
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    º´¿ë±Ý±â :
     
	 °í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
	 
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    | Mechanism of Action | 
    
       Doxycycline¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Doxycycline, like minocycline, is lipophilic and can pass through the lipid bilayer of bacteria. Doxycycline reversibly binds to the 30 S ribosomal subunits and possibly the 50S ribosomal subunit(s), blocking the binding of aminoacyl tRNA to the mRNA and inhibiting bacterial protein synthesis. 
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    | Pharmacology | 
     
       Doxycycline¿¡ ´ëÇÑ Pharmacology Á¤º¸ Doxycycline, a long-acting tetracycline derived from oxytetracycline, is used to inhibit bacterial protein synthesis and treat non-gonococcal urethritis and cervicitis, exacerbations of bronchitis in patients with COPD, and adult periodontitis. 
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    | Metabolism | 
    
       Doxycycline¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 3A43 (CYP3A43) 
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    | Absorption | 
    
       Doxycycline¿¡ ´ëÇÑ Absorption Á¤º¸ Completely absorbed following oral administration. 
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    | Toxicity | 
    
       Doxycycline¿¡ ´ëÇÑ Toxicity Á¤º¸ Symptoms of overdose include anorexia, nausea, diarrhoea, glossitis, dysphagia, enterocolitis and inflammatory lesions (with monilial overgrowth) in the anogenital region, skin reactions such as maculopapular and erythematous rashes, exfoliative dermatitis, photosensitivity, hypersensitivity reactions such as urticaria, angioneurotic oedema, anaphylaxis, anaphyl-actoid purpura, pericarditis, and exacerbation of systemic lupus erythematosus, benign intracranial hypertension in adults disappearing on discontinuation of the medicine, haematologic abnormalities such as haemolytic anaemia, thrombocytopenia, neutropenia, and eosinophilia. LD50=262 mg/kg (I.P. in rat). 
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    | Drug Interactions | 
    
       Doxycycline¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Acitretin	Increased risk of intracranial hypertensionAmobarbital	The anticonvulsant decreases the effect of doxycyclineAmoxicillin	Possible antagonism of actionAmpicillin	Possible antagonism of actionAnisindione	The tetracycline increases the anticoagulant effectAprobarbital	The anticonvulsant decreases the effect of doxycyclineAzlocillin	Possible antagonism of actionAztreonam	Possible antagonism of actionCarbenicillin	Possible antagonism of actionButabarbital	The anticonvulsant decreases the effect of doxycyclineButalbital	The anticonvulsant decreases the effect of doxycyclineButethal	The anticonvulsant decreases the effect of doxycyclineCarbamazepine	The anticonvulsant decreases the effect of doxycyclineClavulanate	Possible antagonism of actionCloxacillin	Possible antagonism of actionCyclacillin	Possible antagonism of actionDicloxacillin	Possible antagonism of actionDicumarol	The tetracycline increases the anticoagulant effectDigoxin	The tetracycline increases the effect of digoxin in 10% of patientsDihydroquinidine barbiturate	The anticonvulsant decreases the effect of doxycyclineEthinyl Estradiol	This anti-infectious agent could decrease the effect  of the oral contraceptiveEthotoin	The anticonvulsant decreases the effect of doxycyclineEtretinate	Increased risk of intracranial hypertensionFlucloxacillin	Possible antagonism of actionFosphenytoin	The anticonvulsant decreases the effect of doxycyclineHeptabarbital	The anticonvulsant decreases the effect of doxycyclineHetacillin	Possible antagonism of actionHexobarbital	The anticonvulsant decreases the effect of doxycyclineInsulin	Tetracycline increases the risk of hypoglycemiaInsulin-aspart	Tetracycline increases the risk of hypoglycemiaInsulin-detemir	Tetracycline increases the risk of hypoglycemiaInsulin-glargine	Tetracycline increases the risk of hypoglycemiaInsulin-glulisine	Tetracycline increases the risk of hypoglycemiaInsulin-lispro	Tetracycline increases the risk of hypoglycemiaIsotretinoin	Increased risk of intracranial hypertensionMephenytoin	The anticonvulsant decreases the effect of doxycyclineMestranol	This anti-infectious agent could decrease the effect of the oral contraceptiveMezlocillin	Possible antagonism of actionMethohexital	The anticonvulsant decreases the effect of doxycyclineMethylphenobarbital	The anticonvulsant decreases the effect of doxycyclineNafcillin	Possible antagonism of actionOxacillin	Possible antagonism of actionPenicillin G	Possible antagonism of actionPenicillin V	Possible antagonism of actionPhenobarbital	The anticonvulsant decreases the effect of doxycyclinePentobarbital	The anticonvulsant decreases the effect of doxycyclinePhenytoin	The anticonvulsant decreases the effect of doxycyclinePiperacillin	Possible antagonism of actionPrimidone	The anticonvulsant decreases the effect of doxycyclineQuinidine barbiturate	The anticonvulsant decreases the effect of doxycyclineRifabutin	The rifamycin decreases the effect of doxycyclineRifampin	The rifamycin decreases the effect of doxycyclineSecobarbital	The anticonvulsant decreases the effect of doxycyclineTalbutal	The anticonvulsant decreases the effect of doxycyclineWarfarin	The tetracycline increases the anticoagulant effectAluminium	Formation of non-absorbable complexesMethotrexate	The tetracycline increases methotrexate toxicityMagnesium oxide	Formation of non-absorbable complexesMagnesium	Formation of non-absorbable complexesAttapulgite	Formation of non-absorbable complexesBacampicillin	Possible antagonism of actionBismuth	Formation of non-absorbable complexesCalcium	Formation of non-absorbable complexesIron	Formation of non-absorbable complexesMeticillin	Possible antagonism of actionZinc	Formation of non-absorbable complexesAcenocoumarol	The tetracycline increases the anticoagulant effectPivampicillin	Possible antagonism of actionPivmecillinam	Possible antagonism of actionTazobactam	Possible antagonism of actionTicarcillin	Possible antagonism of action 
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    CYP450  Drug Interaction | 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] 
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    | Food Interaction | 
    
       Doxycycline¿¡ ´ëÇÑ Food Interaction Á¤º¸ Avoid alcohol.Avoid milk, calcium containing dairy products, iron, antacids, or aluminum salts 2 hours before or 6 hours after using antacids while on this medication.Take with a full glass of water Do not take calcium, aluminum, magnesium or Iron supplements within 2 hours of taking this medication. 
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    | Drug Target | 
    
      
      [Drug Target]
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    | Description | 
    
       Doxycycline¿¡ ´ëÇÑ Description Á¤º¸ A synthetic tetracycline derivative with similar antimicrobial activity. Animal studies suggest that it may cause less tooth staining than other tetracyclines. It is used in some areas for the treatment of chloroquine-resistant falciparum malaria (malaria, falciparum). [PubChem] 
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    | Dosage Form | 
    
       Doxycycline¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Capsule	OralGel, metered	PeriodontalTablet	Oral 
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    | Drug Category | 
    
       Doxycycline¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Bacterial AgentsAntimalarialsTetracyclines 
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    | Smiles String Canonical | 
    
       Doxycycline¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC1C2C(O)C3C(N(C)C)C(=O)C(C(=O)C3(O)C(=O)C2=C(O)C2=C1C=CC=C2O)=C(N)O 
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    | Smiles String Isomeric | 
    
       Doxycycline¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ C[C@@H]1[C@H]2[C@H](O)[C@H]3[C@H](N(C)C)C(=O)\C(C(=O)[C@@]3(O)C(=O)C2=C(O)C2=C1C=CC=C2O)=C(/N)O 
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    | InChI Identifier | 
    
       Doxycycline¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C22H24N2O8/c1-7-8-5-4-6-9(25)11(8)16(26)12-10(7)17(27)14-15(24(2)3)18(28)13(21(23)31)20(30)22(14,32)19(12)29/h4-7,10,14-15,17,25-27,31-32H,23H2,1-3H3/b21-13-/t7-,10+,14+,15-,17-,22-/m0/s1 
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    | Chemical IUPAC Name | 
    
       Doxycycline¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (2Z,4S,4aR,5S,5aR,6R,12aS)-2-(amino-hydroxymethylidene)-4-dimethylamino-5,10,11,12a-tetrahydroxy-6-methyl-4a,5,5a,6-tetrahydro-4H-tetracene-1,3,12-trione 
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                º» ¼öÁ¤ÀÏ Á¤º¸´Â Çã°¡Á¤º¸ ÀÌ¿ÜÀÇ ±âŸÁ¤º¸ ¼öÁ¤ÀÏÀ» ÀǹÌÇϹǷÎ, Çã°¡Á¤º¸¼öÁ¤ÀÏÀº º»¹®¿¡ Ç¥±âµÈ ³¯Â¥¸¦ ÂüÁ¶ÇϽñ⠹ٶø´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. 
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                          ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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