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10mg/min 30ºÐ°£ |
0.75mg/min |
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15mg/min 30ºÐ°£ |
1.00mg/min |
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20mg/min 30ºÐ°£ |
1.25mg/min |
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3) INR(±¹Á¦Á¤»óȺñÀ²)ÀÇ º¯È : ÀÌ ¾àÀ» Æ÷ÇÔÇÑ Ç×»ý¹°ÁúÀ» Ç×ÀÀ°íÁ¦¿Í µ¿½Ã¿¡ Åõ¿© ¹ÞÀº ȯÀÚ¿¡¼ Ç×ÀÀ°í Ȱ¼ºÀÇ Áõ°¡°¡ º¸°íµÇ¾ú´Ù. °¨¿°¼ºÁúȯ(±×¸®°í ¿°Áõ¼º °úÁ¤À» µ¿¹ÝÇÑ), ȯÀÚÀÇ ¿¬·É°ú ÀϹÝÀûÀÎ »óÅ´ À§Çè¿ä¼Ò°¡ µÈ´Ù. ºñ·Ï ÀÌ ¾à°ú ¿ÍÆÄ¸°ÀÇ »óÈ£ÀÛ¿ëÀÌ ÀÓ»ó½ÃÇèÀ» ÅëÇØ ¹àÇôÁöÁö ¾Ê¾ÒÁö¸¸ INR ¸ð´ÏÅ͸µÀ» ½Ç½ÃÇÏ¿©¾ß Çϰí, ÇÊ¿äÇÑ °æ¿ì °æ±¸¿ë Ç×ÀÀ°íÁ¦ÀÇ ¿ë·®À» ÀûÀýÈ÷ Á¶ÀýÇÑ´Ù. Ç×»ý¹°ÁúÀÇ ÀϺΠÁ¾·ùµé, ƯÈ÷ Ç÷ç¿À·ÎÄû³î·Ð, ¸¶Å©·Î¶óÀ̵å, »çÀÌŬ¸°, ÄÚÆ®¸®¸ñ»çÁ¹°ú ÀϺΠ¼¼ÆÈ·Î½ºÆ÷¸°ÀÇ °æ¿ì´Â ´õ ½ÉÇÏ´Ù.
4) CYP3A4 ¹×/¶Ç´Â CYP3A5 ¾ïÁ¦Á¦´Â Ŭ¸°´Ù¸¶À̽ÅÀÇ Ç÷Àå ³óµµ¸¦ Áõ°¡½Ãų ¼ö ÀÖ´Ù. °ÇÑ CYP3A4 ¹×/¶Ç´Â CYP3A5 ¾ïÁ¦Á¦¿Í Ŭ¸°´Ù¸¶À̽ÅÀÇ º´¿ëÅõ¿©½Ã¿¡´Â ÀÌ»ó¹ÝÀÀÀ» ¸ð´ÏÅ͸µ ÇØ¾ß ÇÑ´Ù.
5) CYP3A4 ¹×/¶Ç´Â CYP3A5 À¯µµÁ¦´Â Ŭ¸°´Ù¸¶À̽ÅÀÇ Ç÷Àå ³óµµ¸¦ °¨¼Ò½Ãų ¼ö ÀÖ´Ù. ¸®ÆÊÇǽÅó·³ °ÇÑ CYP3A4 ¹×/¶Ç´Â CYP3A5 À¯µµÁ¦ÀÇ º´¿ëÅõ¿©½Ã¿¡´Â È¿´É »ó½Ç ¿©ºÎ¸¦ ¸ð´ÏÅ͸µ ÇØ¾ß ÇÑ´Ù. |
| Related FDA Approved Drug |
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 FDA : Bµî±Þ
(clindamycinÀº ŹÝÀ» Åë°úÇÑ´Ù. )
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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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¹Ýµå½Ã °ø½Å·Â ÀÖ´Â ¹®ÇåÀ» ´Ù½Ã Çѹø Âü°í ÇϽñ⠹ٶó¸ç ÀÇ»ç ¶Ç´Â ¾à»çÀÇ ÆÇ´Ü¿¡ µû¶ó Åõ¿©¿©ºÎ°¡ °áÁ¤µÇ¾î¾ß ÇÕ´Ï´Ù.
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| DUR (ÀǾàǰ»ç¿ëÆò°¡) |
º´¿ë±Ý±â :
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| Mechanism of Action |
Clindamycin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Systemic/Vaginal-Clindamycin inhibits protein synthesis of bacteria by binding to the 50 S ribosomal subunits of the bacteria. Topical-Clindamycin reduces free fatty acid concentrations on the skin and to suppress the growth of Propionibacterium acnes (Corynebacterium acnes) , an anaerobe found in sebaceous glands and follicles.
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| Pharmacology |
Clindamycin¿¡ ´ëÇÑ Pharmacology Á¤º¸ Clindamycin is an antibiotic, similar to and a derivative of lincomycin. Clindamycin can be used in topical or systemic treatment. It is effective as an anti-anaerobic antibiotic and antiprotozoal.
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| Metabolism |
Clindamycin¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 3A4 (CYP3A4)
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| Protein Binding |
Clindamycin¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 92-94%
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| Half-life |
Clindamycin¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 2.4 hours
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| Absorption |
Clindamycin¿¡ ´ëÇÑ Absorption Á¤º¸ Rapidly absorbed after oral administration. Absorption of an oral dose is virtually complete (90%), and the concomitant administration of food does not appreciably modify the serum concentrations; serum levels have been uniform and predictable from person to person and dose to dose.
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| Biotransformation |
Clindamycin¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic
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| Toxicity |
Clindamycin¿¡ ´ëÇÑ Toxicity Á¤º¸ Orally and parenterally administered clindamycin has been associated with severe colitis (pseudomembranous colitis) which may result in patient death. Use of the topical formulation of clindamycin results in absorption of the antibiotic from the skin surface. Diarrhea, bloody diarrhea, and colitis (including pseudomembranous colitis) have been reported with the use of topical and systemic clindamycin.
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| Drug Interactions |
Clindamycin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Aluminium The aluminium salt decreases the absorption of lincosamidesAtracurium The agent increases the effect of muscle relaxantDihydroxyaluminium The aluminium salt decreases the absorption of lincosamidesCyclosporine Decreases the effect of cyclosporineDoxacurium The agent increases the effect of muscle relaxantGallamine Triethiodide The agent increases the effect of muscle relaxantMetocurine The agent increases the effect of muscle relaxantMivacurium The agent increases the effect of muscle relaxantPancuronium The agent increases the effect of muscle relaxantPipecuronium The agent increases the effect of muscle relaxantRocuronium The agent increases the effect of muscle relaxantSuccinylcholine The agent increases the effect of muscle relaxantTubocurarine The agent increases the effect of muscle relaxantVecuronium The agent increases the effect of muscle relaxantAttapulgite The aluminium salt decreases the absorption of lincosamidesKaolin The aluminium salt decreases the absorption of lincosamides
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Clindamycin¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take with food.
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| Drug Target |
[Drug Target]
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| Description |
Clindamycin¿¡ ´ëÇÑ Description Á¤º¸ An antibacterial agent that is a semisynthetic analog of lincomycin. [PubChem]
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| Dosage Form |
Clindamycin¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Capsule OralCream IntravaginalCream TopicalLiquid IntramuscularLiquid IntravenousPowder, for solution OralSolution IntravenousSolution Topical
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| Drug Category |
Clindamycin¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Bacterial AgentsLincomycinsProtein Synthesis Inhibitors
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| Smiles String Canonical |
Clindamycin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CCCC1CC(N(C)C1)C(=O)NC(C(C)Cl)C1OC(SC)C(O)C(O)C1O
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| Smiles String Isomeric |
Clindamycin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CCC[C@@H]1C[C@H](N(C)C1)C(=O)N[C@H]([C@H](C)Cl)[C@H]1O[C@H](SC)[C@H](O)[C@@H](O)[C@H]1O
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| InChI Identifier |
Clindamycin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C18H33ClN2O5S/c1-5-6-10-7-11(21(3)8-10)17(25)20-12(9(2)19)16-14(23)13(22)15(24)18(26-16)27-4/h9-16,18,22-24H,5-8H2,1-4H3,(H,20,25)/t9?,10-,11+,12?,13+,14-,15-,16-,18-/m1/s1/f/h20H
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| Chemical IUPAC Name |
Clindamycin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (2S,4R)-N-[2-chloro-1-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methylsulfanyloxan-2-yl]propyl]-1-methyl-4-propylpyrrolidine-2-carboxamide
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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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»ó¼¼Á¤º¸´Â ½ÄǰÀǾàǰ¾ÈÀüóÀÇ Á¦Ç°Çã°¡»çÇ×À» Åä´ë·Î ÀÛ¼ºµÇ¾úÀ¸¸ç ¿ä¾àÁ¤º¸´Â »ó¼¼Á¤º¸ ¹× ±âŸ¹®ÇåÀ» ±â¹ÝÀ¸·Î µå·°ÀÎÆ÷¿¡¼ ÆíÁýÇÑ ³»¿ëÀÔ´Ï´Ù. Á¦Ç°Çã°¡»çÇ×ÀÇ ¸ñÂ÷¿Í ´Ù¼Ò »óÀÌÇÒ ¼ö ÀÖ½À´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
Ã¥ÀÓÀ» ÁöÁö ¾Ê½À´Ï´Ù. ÀÚ¼¼ÇÑ ³»¿ëÀº ¡°Ã¥ÀÓÀÇ ÇÑ°è ¹× ¹ýÀû°íÁö¡±¸¦ ÂüÁ¶ÇØ ÁֽʽÿÀ.
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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