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    | Mechanism of Action | 
    
       Levofloxacin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Levofloxacin inhibits bacterial type II topoisomerases, topoisomerase IV and DNA gyrase. Levofloxacin, like other fluoroquinolones, inhibits the A subunits of DNA gyrase, two subunits encoded by the gyrA gene. This results in strand breakage on a bacterial chromosome, supercoiling, and resealing; DNA replication and transcription is inhibited. 
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       Levofloxacin¿¡ ´ëÇÑ Pharmacology Á¤º¸ Levofloxacin, a fluoroquinolone antiinfective, is the optically active L-isomer of ofloxacin. Levofloxacin is used to treat bacterial conjunctivitis, sinusitis, chronic bronchitis, community-acquired pneumonia and pneumonia caused by penicillin-resistant strains of Streptococcus pneumoniae, skin and skin structure infections, complicated urinary tract infections and acute pyelonephritis. 
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       Levofloxacin¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 1A2 (CYP1A2) 
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       Levofloxacin¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 24-38% (to plasma proteins) 
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       Levofloxacin¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 6-8 hours 
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       Levofloxacin¿¡ ´ëÇÑ Absorption Á¤º¸ Absorption of ofloxacin after single or multiple doses of 200 to 400 mg is predictable, and the amount of drug absorbed increases proportionately with the dose. 
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´Ü¹é°áÇÕ : 24-38%
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¹Ý°¨±â : 6-8 ½Ã°£ 
  -  ¼Ò½Ç : ÁÖ·Î ¹Ìº¯Èü·Î ½Å¹è¼³, 4% ¹Ì¸¸ÀÌ º¯¹è¼³
   
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    | Biotransformation | 
    
       Levofloxacin¿¡ ´ëÇÑ Biotransformation Á¤º¸ Not Available 
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    | Toxicity | 
    
       Levofloxacin¿¡ ´ëÇÑ Toxicity Á¤º¸ Side effects include disorientation, dizziness, drowsiness, hot and cold flashes, nausea, slurring of speech, swelling and numbness in the face 
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    | Drug Interactions | 
    
       Levofloxacin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Aluminium	Formation of non-absorbable complexesBismuth	Formation of non-absorbable complexesCalcium	Formation of non-absorbable complexesIron	Formation of non-absorbable complexesMagnesium oxide	Formation of non-absorbable complexesMagnesium	Formation of non-absorbable complexesSucralfate	Formation of non-absorbable complexesZinc	Formation of non-absorbable complexesAmiodarone	Increased risk of cardiotoxicity and arrhythmiasBepridil	Increased risk of cardiotoxicity and arrhythmiasBretylium	Increased risk of cardiotoxicity and arrhythmiasChlorpromazine	Increased risk of cardiotoxicity and arrhythmiasDihydroquinidine barbiturate	Increased risk of cardiotoxicity and arrhythmiasDisopyramide	Increased risk of cardiotoxicity and arrhythmiasErythromycin	Increased risk of cardiotoxicity and arrhythmiasFluphenazine	Increased risk of cardiotoxicity and arrhythmiasJosamycin	Increased risk of cardiotoxicity and arrhythmiasMesoridazine	Increased risk of cardiotoxicity and arrhythmiasMethotrimeprazine	Increased risk of cardiotoxicity and arrhythmiasPerphenazine	Increased risk of cardiotoxicity and arrhythmiasProchlorperazine	Increased risk of cardiotoxicity and arrhythmiasQuinidine	Increased risk of cardiotoxicity and arrhythmiasPropiomazine	Increased risk of cardiotoxicity and arrhythmiasPromazine	Increased risk of cardiotoxicity and arrhythmiasPromethazine	Increased risk of cardiotoxicity and arrhythmiasProcainamide	The quinolone increases the effect of procainamideQuinidine barbiturate	Increased risk of cardiotoxicity and arrhythmiasQuinupristin	This combination presents an increased risk of toxicitySotalol	Increased risk of cardiotoxicity and arrhythmiasThiethylperazine	Increased risk of cardiotoxicity and arrhythmiasThioridazine	Increased risk of cardiotoxicity and arrhythmiasTrifluoperazine	Increased risk of cardiotoxicity and arrhythmiasTriflupromazine	Increased risk of cardiotoxicity and arrhythmiasWarfarin	The quinolone increases the anticoagulant effectAcenocoumarol	The quinolone increases the anticoagulant effectDicumarol	The quinolone increases the anticoagulant effectAnisindione	The quinolone increases the anticoagulant effect 
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    CYP450  Drug Interaction | 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] 
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    | Food Interaction | 
    
       Levofloxacin¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take without regard to meals. Take with water, drink lliberally. Taking this product with orange juice can result in reduced quinolone plasma levels. 
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    | Drug Target | 
    
      
      [Drug Target]
     | 
   
  
   
    | Description | 
    
       Levofloxacin¿¡ ´ëÇÑ Description Á¤º¸ A synthetic fluoroquinolone (fluoroquinolones) antibacterial agent that inhibits the supercoiling activity of bacterial DNA gyrase, halting DNA replication. [PubChem] 
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    | Dosage Form | 
    
       Levofloxacin¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Solution	IntravenousTablet	Oral 
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    | Drug Category | 
    
       Levofloxacin¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Bacterial AgentsAnti-Infective Agents, UrinaryNucleic Acid Synthesis InhibitorsQuinolones 
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    | Smiles String Canonical | 
    
       Levofloxacin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC1COC2=C3N1C=C(C(O)=O)C(=O)C3=CC(F)=C2N1CCN(C)CC1 
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    | Smiles String Isomeric | 
    
       Levofloxacin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ C[C@H]1COC2=C3N1C=C(C(O)=O)C(=O)C3=CC(F)=C2N1CCN(C)CC1 
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    | InChI Identifier | 
    
       Levofloxacin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C18H20FN3O4/c1-10-9-26-17-14-11(16(23)12(18(24)25)8-22(10)14)7-13(19)15(17)21-5-3-20(2)4-6-21/h7-8,10H,3-6,9H2,1-2H3,(H,24,25)/t10-/m0/s1/f/h24H 
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    | Chemical IUPAC Name | 
    
       Levofloxacin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (-)-(S)-9-fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7Hpyrido[1,2,3-de]-1,4 benzoxazine-6-carboxylic acid hemihydrate 
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                            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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