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ÀÌ ¾àÀº Æä´Ï½Ç¸° ¾Ë·¹¸£±â°¡ Àִ ȯÀÚ ¶Ç´Â Æä´Ï½Ç¸° »ç¿ëÀÌ ÀûÀýÇÏÁö ¾ÊÀº ȯÀÚ¿¡´Â ÀÇ»çÀÇ ÆÇ´Ü ÇÏ¿¡ »ç¿ëÇÏ¿©¾ß ÇÑ´Ù.
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1) ¸°ÄÚ¸¶À̽ÅÀ̳ª Ŭ¸°´Ù¸¶À̽ſ¡ °ú¹Î¹ÝÀÀÀÇ º´·ÂÀÌ Àִ ȯÀÚ
2) ÀÌ ¾àÀº À¯´çÀ» ÇÔÀ¯Çϰí ÀÖÀ¸¹Ç·Î, °¥¶ôÅä¿À½º ºÒ³»¼º(galactose intolerance), Lapp À¯´çºÐÇØÈ¿¼Ò °áÇÌÁõ(Lapp lactase deficiency) ¶Ç´Â Æ÷µµ´ç-°¥¶ôÅä¿À½º Èí¼öÀå¾Ö(glucose-galactose malabsorption) µîÀÇ À¯ÀüÀûÀÎ ¹®Á¦°¡ Àִ ȯÀÚ¿¡°Ô´Â Åõ¿©ÇÏ¸é ¾È µÈ´Ù.
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2) ´ëÀå¿° µîÀÇ º´·ÂÀÌ Àִ ȯÀÚ(À§¸·¼º´ëÀå¿° µî ½É°¢ÇÑ ´ëÀå¿°ÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.)
3) °£Àå¾Ö ¶Ç´Â ±× º´·ÂÀÌ Àִ ȯÀÚ(´ãÁó¹è¼³ÀÌ µÇ¹Ç·Î ¼Ò½Ç¹Ý°¨±â°¡ ¿¬ÀåµÉ ¼ö ÀÖ´Ù.)
4) ½ÅÀå¾Ö ¶Ç´Â ±× º´·ÂÀÌ Àִ ȯÀÚ(½ÅÀåÀÌ ÀÌ ¾àÀÇ ÁÖ ¹è¼³°æ·Î´Â ¾Æ´ÏÁö¸¸, ¼Ò½Ç¹Ý°¨±â°¡ ¿¬ÀåµÉ ¼ö ÀÖ´Ù.)
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6) ½ÄµµÅë°úÀå¾Ö ȯÀÚ(½Äµµ¿¡ Á¤·ù ½Ã ºØ±«ÇÏ¿© ½Äµµ±Ë¾çÀ» ÀÏÀ¸Å³ ¼ö ÀÖ´Ù.)
7) õ½Ä, ¾à¹° ¶Ç´Â ±âŸ ¾Ë·¹¸£±âÇ׿ø¿¡ °ú¹Î¹ÝÀÀÀÇ º´·ÂÀÌ Àִ ȯÀÚ
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1) ¼Òȱâ°è : ¶§¶§·Î À§¸·¼º´ëÀå¿° µî Ç÷º¯À» µ¿¹ÝÇÑ ´ëÀå¿°, ¼³»ç, ¹±Àº º¯, ½Ä¿åºÎÁø, ±¸¿ª, ±¸Åä, º¹Åë, ½Äµµ¿°, ¼³¿°, ±¸³»¿°, ½Äµµ±Ë¾çÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
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3) ÇǺΠ¹× ÇÇÇÏÁ¶Á÷ : ¹Ý±¸Áø¼º¹ßÁø, µÎµå·¯±â, È«¿ª¾çÇǺιßÁø, ºÎÁ¾, °¡·Á¿ò, Áú¿°, ¹ÚÅ» ¹× ´ë¼Ò¼öÆ÷¼ºÇǺο°, ¸Æ°üºÎÁ¾ ¹× Æä´Ï½Ç¸° ¾Ë·¹¸£±â ¹ÝÀÀ°ú °°Àº ¾Æ³ªÇʶô½Ã µîÀÇ °ú¹Î¹ÝÀÀÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÀÌ·¯ÇÑ Áõ»óÀÌ ³ªÅ¸³¯ °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇϸç ÁßÁõÀÎ °æ¿ì¿¡´Â º¸Åë »ç¿ëµÇ´Â ÀÀ±Þóġ¾à(¿¡Çdz×ÇÁ¸°, ÄÚ¸£Æ¼ÄÚÀ̵å, Ç×È÷½ºÅ¸¹ÎÁ¦ µî)À» Åõ¿©ÇÑ´Ù. µå¹°°Ô ½ºÆ¼ºì½º-Á¸½¼ÁõÈıº, µ¶¼ºÇ¥ÇDZ«»ç¿ëÇØ, ´ÙÇüÈ«¹Ý, ±Þ¼º Àü½Å¼º ¹ßÁø¼º ³óÆ÷Áõ(AGEP), ¾à¹°°ú¹Î¹ÝÀÀÁõÈıº(Drug rash with eosinophilia and systemic symptom(DRESS) ¶Ç´Â Drug-induced hypersensitivity syndrome(DIHS))ÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÃæºÐÈ÷ °üÂûÇϰí ÀÌ·¯ÇÑ Áõ»óÀÌ ³ªÅ¸³ª´Â °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇϰí ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù.
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5) ½ÅÀå : Å©·¹¾ÆÆ¼´Ñ, BUN, NPNÀÇ »ó½Â, µå¹°°Ô Áú¼ÒÇ÷Áõ, ÇÌ´¢ ¶Ç´Â ´Ü¹é´¢·Î µå·¯³ª´Â ½Å±â´ÉÀå¾Ö°¡ °üÂûµÈ ¹Ù ÀÖÀ¸¹Ç·Î Àå±âÅõ¿©ÀÎ °æ¿ì¿¡´Â Á¤±âÀûÀÎ ½Å±â´É°Ë»ç°¡ ÇÊ¿äÇÏ´Ù. À¯»ç¾à(ÀλêŬ¸°´Ù¸¶À̽Å)¿¡¼ ±Þ¼º ½ÅºÎÀüÀÌ ³ªÅ¸³µ´Ù´Â º¸°í°¡ ÀÖÀ¸¹Ç·Î, °üÂûÀ» ÃæºÐÈ÷ Çϰí, ÀÌ»ó¹ÝÀÀÀÌ ³ªÅ¸³ª´Â °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇÏ´Â µî ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù.
6) ±Ù°ñ°Ý°è : ´Ù¹ß¼º °üÀý¿°ÀÌ º¸°íµÈ ¹Ù ÀÖ´Ù.
7) Ç÷¾× ¹× ¸²ÇÁ°è : µå¹°°Ô È£Áß±¸ °¨¼Ò, È£»ê±¸ Áõ°¡, ¹éÇ÷±¸ °¨¼Ò, ¹«°ú¸³±¸Áõ, Ç÷¼ÒÆÇ°¨¼Ò¼º ÀÚ¹Ý, Àç»ýºÒ·®¼ººóÇ÷, °ú¸³±¸ °¨¼Ò, ¹éÇ÷±¸ Áõ°¡ µî Ç÷¾×Àå¾Ö°¡ ³ªÅ¸³µ´Ù. À¯»ç¾à(ÀλêŬ¸°´Ù¸¶À̽Å)¿¡¼ ¹üÇ÷±¸ °¨¼Ò, Ç÷¼ÒÆÇ °¨¼Ò°¡ ³ªÅ¸³µ´Ù´Â º¸°í°¡ ÀÖÀ¸¹Ç·Î Àå±âÅõ¿©¸¦ ÇÏ´Â °æ¿ì¿¡´Â Ç÷¾×°Ë»ç µî °üÂûÀ» ÃæºÐÈ÷ Çϰí, ÀÌ»ó¹ÝÀÀÀÌ ³ªÅ¸³ª´Â °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇÏ´Â µî ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù. À§ ¹ÝÀÀµé°ú Ŭ¸°´Ù¸¶À̽Šġ·á¿ÍÀÇ Á÷Á¢ÀûÀÎ Àΰú°ü°è´Â ¹àÇôÁöÁö ¾Ê¾Ò´Ù.
8) ½Å°æ°è : À̸í, ¾îÁö·¯¿òÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
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3) ¾Ë·ç¹Ì´½(¼ö»ê¿°)ÀÇ °æ¿ì´Â Ŭ¸°´Ù¸¶À̽ÅÀÇ À§Àå°ü Èí¼ö¸¦ ÀúÇϽÃŰ¹Ç·Î Ŭ¸°´Ù¸¶À̽Űú º°µµ·Î(°¡´ÉÇϸé 2½Ã°£°¡·® Àü¿¡) À§Àå¾àÀ» º¹¿ëÇÑ´Ù.
4) 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.
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±ÍÇϰ¡ º¹¾àÀ̹ÌÁö Á¤º¸¸¦ ½Å·ÚÇÔÀº ÀüÀûÀ¸·Î ±ÍÇÏÀÇ Ã¥ÀÓÀÔ´Ï´Ù. µå·°ÀÎÆ÷´Â ÀÌ¿¡ ´ëÇÑ ¾î¶°ÇÑ º¸Áõµµ ÇÏÁö ¾Ê½À´Ï´Ù. |
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| º¸°ü»ó ÁÖÀÇ |
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| Ç׸ñ |
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| DUR (ÀǾàǰ»ç¿ëÆò°¡) |
º´¿ë±Ý±â :
°í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
[»óÈ£ÀÛ¿ë/º´¿ë±Ý±â°Ë»ö]
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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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»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
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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