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·¹º¸Æå½ÅÁ¡¾È¾×(·¹º¸Ç÷ϻç½Å) 5mL LEVOFEXIN EYE DROPS[Levofloxacin]
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642900241
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\3,335 ¿ø/5mL/º´(2017.02.01)(ÇöÀç¾à°¡)
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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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| Pharmacology |
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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| Metabolism |
Levofloxacin¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 1A2 (CYP1A2)
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| Protein Binding |
Levofloxacin¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 24-38% (to plasma proteins)
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| Half-life |
Levofloxacin¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 6-8 hours
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| Absorption |
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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| Pharmacokinetics |
LevofloxacinÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
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Èí¼ö : Àß Èí¼öµÈ´Ù. À½½Ä¹°¿¡ ÀÇÇÑ ¿µÇâÀº ¹Ì¹ÌÇÏ´Ù.
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»ýü³»ÀÌ¿ë·ü : 99%
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ºÐÆ÷ : ºÐÆ÷¿ëÀû : 1.25 L/kg
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´ë»ç : ÀÔüÈÇÐÀûÀ¸·Î Ç÷Àå°ú ¼Òº¯Áß¿¡¼ ¾ÈÁ¤Çϸç, À̰ÍÀÇ enantiomer·Î´Â ´ë»çÀûÀ¸·Î º¯È¯µÇÁö ¾Ê´Â´Ù.
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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]
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| 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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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.
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
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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