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2) ÇÁ·Îº£³×½Ãµå¿Í º´¿ë Åõ¿©½Ã ÀÌ ¾àÀÇ ÀÛ¿ëÀÌ Áõ°µÉ ¼ö ÀÖÀ¸¹Ç·Î °¨·®ÇÏ´Â µî ½ÅÁßÈ÷ Åõ¿©ÇÑ´Ù
3) Æ®¸®¾ÏÅ×·»°ú º´¿ë Åõ¿©½Ã »óÈ£ ÀÌ»ó¹ÝÀÀÀÌ Áõ°¡µÉ ¼ö ÀÖÀ¸¹Ç·Î º´¿ëÅõ¿©ÇÏÁö ¾Ê´Â´Ù. (Áú¼ÒÇ÷Áõ, Å©·¹¾ÆÆ¼´Ñ û¼ÒÀ²ÀÇ ÀúÇϰ¡ »ý±æ ¼ö ÀÖ´Ù.)
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5) ÀÌ ¾àÀº »çÀÌŬ·Î¿Á½Ã°Ô³ªÁ¦-2(cyclooxygenase-2)¼±ÅÃÀû ÀúÇØÁ¦¸¦ Æ÷ÇÔÇÏ¿© ´Ù¸¥ ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°ÁøÅëÁ¦(NSAIDs)¿Í º´¿ëÅõ¿©ÇÒ °æ¿ì ÀÌ»ó¹ÝÀÀÀÇ À§ÇèÀÌ Áõ°¡ÇÒ¼ö ÀÖÀ¸¹Ç·Î º´¿ëÅõ¿©ÇÏÁö ¾Ê´Â´Ù.
6) ¥â-Â÷´ÜÁ¦, İÅäÇÁ¸±, ¿¡³¯¶óÇÁ¸±, Ä¡¾ÆÁþ°è ÀÌ´¢°¾ÐÁ¦,Ǫ·Î¼¼¹Ìµå¿Í º´¿ëÅõ¿©½Ã ±× ÀÛ¿ëÀ» ÀúÇϽÃų ¼ö ÀÖÀ¸¹Ç·Î ½ÅÁßÈ÷ Åõ¿©ÇÑ´Ù.
7) ACE ÀúÇØÁ¦ : ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°ÁøÅëÁ¦¿¡ÀÇÇØ ACE ÀúÇØÁ¦ÀÇ Ç×°íÇ÷¾ÐÈ¿°ú°¡ °¨¼ÒµÉ ¼ö ÀÖ´Ù´Â º¸°í°¡ ÀÖÀ¸¹Ç·Î ÀÌ ¾à°ú ACE ÀúÇØÁ¦¸¦ º´¿ëÅõ¿©ÇÏ´Â °æ¿ì ÀÌ·¯ÇÑ »óÈ£ÀÛ¿ëÀ» ¿°µÎ¿¡ µÎ¾î¾ß ÇÑ´Ù.
8) Ǫ·Î¼¼¹Ìµå : ÀÓ»ó½ÃÇè ¹× ½ÃÆÇÈÄ Á¶»ç °á°úÀÌ ¾àÀÇ ½ÅÀå¿¡¼ÀÇ ÇÁ·Î½ºÅ¸±Û¶õµò ÇÕ¼º ¾ïÁ¦¿¡ ÀÇÇØ ÀϺΠȯÀÚ¿¡¼ Ǫ·Î¼¼¹Ìµå ¹× Ä¡¾ÆÁþ°è ÀÌ´¢Á¦ÀÇ ³ªÆ®·ý´¢¹è¼³ È¿°ú°¡ °¨¼ÒÇÒ ¼ö ÀÖÀ½ÀÌ È®ÀεǾú´Ù. ÀÌµé ¾à¹°°ú ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°ÁøÅëÁ¦¸¦ º´¿ëÅõ¿©ÇÏ´Â µ¿¾È ½ÅºÎÀü ¡Èĸ¦ ¸é¹ÐÈ÷ °üÂûÇØ¾ß ÇÑ´Ù.
9) ¾Æ½ºÇǸ° : ¾Æ½ºÇǸ°°úÀÇ º´¿ëÀÌ ºñ½ºÅ×·ÎÀ̵强¼Ò¿°ÁøÅëÁ¦ÀÇ »ç¿ë°ú °ü·ÃµÈ Áß´ëÇÑ ½ÉÇ÷°ü°è Ç÷Àü¹ÝÀÀÀÇ À§ÇèÀ» °¨¼Ò½Ãų ¼ö ÀÖ´Ù´Â ÀϰüµÈ Áõ°Å´Â ¾ø´Ù. ´Ù¸¥ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°ÁøÅëÁ¦¿Í ¸¶Âù°¡Áö·Î ÀÌ ¾à°ú ¾Æ½ºÇǸ°ÀÇ º´¿ë¿¡ ÀÇÇØ ÁßÁõÀÇ À§Àå°ü°è ÀÌ»ó¹ÝÀÀÀÇ ¹ß»ý À§ÇèÀÌ Áõ°¡µÉ ¼ö ÀÖÀ¸¹Ç·Î µÎ ¾à¹°ÀÇ º´¿ëÀºÀϹÝÀûÀ¸·Î ±ÇÀåµÇÁö ¾Ê´Â´Ù. ¶ÇÇÑ ¾Æ½ºÇǸ°°ú º´¿ë Åõ¿©½Ã ÀÌ ¾àÀÇ ÀÛ¿ëÀÌ ÀúÇ쵃 ¼ö ÀÖ´Ù.
10) ¸®Æ¬ : ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°ÁøÅëÁ¦´Â ½ÅÀå¿¡¼ÀÇÇÁ·Î½ºÅ¸±Û¶õµò ÇÕ¼º ¾ïÁ¦¿¡ ÀÇÇØ Ç÷û ¸®Æ¬ÀÇ ³óµµ¸¦ Áõ°¡½ÃŰ°í ¸®Æ¬ÀÇ ½ÅŬ¸®¾î·±½º¸¦ °¨¼Ò½Ãų ¼ö ÀÖ´Ù. µû¶ó¼ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°ÁøÅëÁ¦¿Í ¸®Æ¬ÀÇ º´¿ë Åõ¿© ½Ã ¸®Æ¬ÀÇ µ¶¼º ¡Èĸ¦ ÁÖÀDZí°Ô °üÂûÇØ¾ß ÇÑ´Ù.
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12) ¸ÞÅ䯮·º¼¼ÀÌÆ® : ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°ÁøÅëÁ¦(NSAIDs)¿ÍÀÇ º´¿ëÅõ¿©·Î ½Å¼¼´¢°ü¿¡¼ ¸ÞÅ䯮·º¼¼ÀÌÆ®ÀÇ ¹è¼³ÀÌ Áö¿¬µÇ¾î Ä¡¸íÀûÀÎ ¸ÞÅ䯮·º¼¼ÀÌÆ®ÀÇ Ç÷¾×ÇÐÀû µ¶¼ºÀÌÁõ°¡µÉ ¼ö ÀÖÀ¸¹Ç·Î Ç׾Ͽä¹ýÀ¸·Î »ç¿ëÇÏ´Â °í¿ë·®(15mg/ÁÖ ÀÌ»ó)ÀǸÞÅ䯮·º¼¼ÀÌÆ®¿Í´Â º´¿ëÅõ¿©ÇÏÁö ¾ÊÀ¸¸ç, Àú¿ë·®ÀÇ ¸ÞÅ䯮·º¼¼ÀÌÆ®¿Í º´¿ëÅõ¿©½Ã ½ÅÁßÈ÷ Åõ¿©ÇÏ¿©¾ß ÇÑ´Ù.
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| DUR (ÀǾàǰ»ç¿ëÆò°¡) |
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°í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
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Indomethacin¿¡ ´ëÇÑ µ¶¼ºÁ¤º¸ : Á¤º¸º¸±â
Ãâó: ±¹¸³µ¶¼º°úÇпø µ¶¼º¹°ÁúÁ¤º¸DB : http://www.nitr.go.kr/nitr/contents/m134200/view.do |
| Mechanism of Action |
Indomethacin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Antiinflammatory effects of Indomethacin are believed to be due to inhibition of cylooxygenase in platelets which leads to the blockage of prostaglandin synthesis. Antipyretic effects may be due to action on the hypothalamus, resulting in an increased peripheral blood flow, vasodilation, and subsequent heat dissipation.
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| Pharmacology |
Indomethacin¿¡ ´ëÇÑ Pharmacology Á¤º¸ Indomethacin, a nonsteroidal antiinflammatory drug (NSAID) with analgesic and antipyretic properties, is used to treat osteoarthritis and control acute pain.
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| Protein Binding |
Indomethacin¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 97%
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| Half-life |
Indomethacin¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 4.5 hours
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| Absorption |
Indomethacin¿¡ ´ëÇÑ Absorption Á¤º¸ Bioavailability is approximately 100% following oral administration and 80??0% following rectal administration.
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| Pharmacokinetics |
IndomethacinÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- ÀÛ¿ë¹ßÇö½Ã°£ : 30ºÐ À̳»
- ÀÛ¿ëÁö¼Ó½Ã°£ : 4-6 ½Ã°£
- Èí¼ö : ½Å¼ÓÇϰÔ, ¸¹Àº ¾çÀÌ Èí¼öµÊ
- ºÐÆ÷ : ºÐÆ÷¿ëÀû : 0.34-1.57 L/kg. ÅÂ¹Ý Åë°ú, À¯Áó ºÐºñ
- ´Ü¹é°áÇÕ : 90%
- ´ë»ç : °£´ë»ç, Àå°£¼øÈ¯
- ¹Ý°¨±â : 4.5 ½Ã°£. ½Å»ý¾Æ¿¡¼´Â ¿¬ÀåµÊ
- Ç÷ÁßÃÖ°í³óµµ µµ´Þ½Ã°£ : °æ±¸ : 3-4 ½Ã°£ À̳»
- ¼Ò½Ç : Àå°£¼øÈ¯ Å. ÁÖ·Î glucuronide Æ÷ÇÕü·Î¼ ½Å¹è¼³
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| Biotransformation |
Indomethacin¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic.
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| Toxicity |
Indomethacin¿¡ ´ëÇÑ Toxicity Á¤º¸ The following symptoms may be observed following overdosage: nausea, vomiting, intense headache, dizziness, mental confusion, disorientation, or lethargy. There have been reports of paresthesias, numbness, and convulsions. The oral LD50 of indomethacin in mice and rats (based on 14 day mortality response) was 50 and 12 mg/kg, respectively.
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| Drug Interactions |
Indomethacin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Acebutolol Risk of inhibition of renal prostaglandinsAtenolol Risk of inhibition of renal prostaglandinsBetaxolol Risk of inhibition of renal prostaglandinsBevantolol Risk of inhibition of renal prostaglandinsBisoprolol Risk of inhibition of renal prostaglandinsCarteolol Risk of inhibition of renal prostaglandinsCarvedilol Risk of inhibition of renal prostaglandinsMethotrexate The NSAID increases the effect and toxicity of methotrexateDiflunisal Diflunisal increases the effect and toxicity of indomethacinEsmolol Risk of inhibition of renal prostaglandinsLabetalol Risk of inhibition of renal prostaglandinsMetoprolol Risk of inhibition of renal prostaglandinsNadolol Risk of inhibition of renal prostaglandinsLosartan Indomethacin decreases the effect of losartanLithium The NSAID increases serum levels of lithiumOxprenolol Risk of inhibition of renal prostaglandinsPenbutolol Risk of inhibition of renal prostaglandinsPindolol Risk of inhibition of renal prostaglandinsPractolol Risk of inhibition of renal prostaglandinsProbenecid Probenecid increases the effect/toxicity of indomethacinSotalol Risk of inhibition of renal prostaglandinsPropranolol Risk of inhibition of renal prostaglandinsTimolol Risk of inhibition of renal prostaglandinsWarfarin The NSAID increases the anticoagulant effectAcenocoumarol The NSAID increases the anticoagulant effectDicumarol The NSAID increases the anticoagulant effectAnisindione The NSAID increases the anticoagulant effectTorasemide The NSAID decreases the diuretic and antihypertensive effects of the loop diureticBumetanide The NSAID decreases the diuretic and antihypertensive effects of the loop diureticFurosemide The NSAID decreases the diuretic and antihypertensive effects of the loop diureticEthacrynic acid The NSAID decreases the diuretic and antihypertensive effects of the loop diureticCyclosporine Monitor for nephrotoxicityAlendronate Increased risk of gastric toxicityTriamterene Risk of acute renal impairment with this combination
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Drug Target |
[Drug Target]
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| Description |
Indomethacin¿¡ ´ëÇÑ Description Á¤º¸ A non-steroidal anti-inflammatory agent (NSAID) that inhibits the enzyme cyclooxygenase necessary for the formation of prostaglandins and other autacoids. It also inhibits the motility of polymorphonuclear leukocytes. [PubChem]
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| Dosage Form |
Indomethacin¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Capsule OralPowder, for solution IntravenousSuppository Rectal
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| Drug Category |
Indomethacin¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Inflammatory Agents, Non-SteroidalAnti-inflammatory AgentsCardiovascular AgentsCyclooxygenase InhibitorsGout SuppressantsNonsteroidal Antiinflammatory Agents (NSAIDs)Tocolytic Agents
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| Smiles String Canonical |
Indomethacin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ COC1=CC2=C(C=C1)N(C(=O)C1=CC=C(Cl)C=C1)C(C)=C2CC(O)=O
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| Smiles String Isomeric |
Indomethacin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ COC1=CC2=C(C=C1)N(C(=O)C1=CC=C(Cl)C=C1)C(C)=C2CC(O)=O
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| InChI Identifier |
Indomethacin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C19H16ClNO4/c1-11-15(10-18(22)23)16-9-14(25-2)7-8-17(16)21(11)19(24)12-3-5-13(20)6-4-12/h3-9H,10H2,1-2H3,(H,22,23)/f/h22H
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| Chemical IUPAC Name |
Indomethacin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methylindol-3-yl]acetic acid
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| Drug-Induced Toxicity Related Proteins |
INDOMETHACIN ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸ Replated Protein:Tumor necrosis factor receptor superfamily member 1A (TNF-R1) Drug:indomethacin Toxicity:gastric damage and granulocyte infiltration. [¹Ù·Î°¡±â] Replated Protein:Plasma kallikrein Drug:indomethacin Toxicity:enterocolitis. [¹Ù·Î°¡±â] Replated Protein:Heat shock 70 kDa protein Drug:indomethacin Toxicity:denatured proteins. [¹Ù·Î°¡±â] Replated Protein:c-myc oncogene Drug:indomethacin Toxicity:apoptosis by indomethacin. [¹Ù·Î°¡±â] Replated Protein:Acetylcholinesterase Drug:indomethacin Toxicity:enhance contractility of the small intestine. [¹Ù·Î°¡±â] Replated Protein:G1/S-specific cyclin-D1 Drug:indomethacin Toxicity:arrests endothelial cell proliferation. [¹Ù·Î°¡±â] Replated Protein:Acetylcholinesterase Drug:indomethacin Toxicity:enhance contractility of the small intestine. [¹Ù·Î°¡±â] Replated Protein:P-selectin Drug:indomethacin Toxicity:Indomethacin induced gastropathy. [¹Ù·Î°¡±â] Replated Protein:B2 bradykinin receptor Drug:indomethacin Toxicity:enterocolitis. [¹Ù·Î°¡±â] Replated Protein:Nitric oxide synthase, inducible Drug:indomethacin Toxicity:gastric damage and granulocyte infiltration. [¹Ù·Î°¡±â] Replated Protein:Intercellular adhesion molecule 1 Drug:indomethacin Toxicity:Indomethacin induced gastropathy. [¹Ù·Î°¡±â] Replated Protein:Plasma kallikrein Drug:indomethacin Toxicity:enterocolitis. [¹Ù·Î°¡±â] Replated Protein:Integrin alpha-M Drug:indomethacin Toxicity:experimental dystonia. [¹Ù·Î°¡±â] Replated Protein:Tumor necrosis factor Drug:indomethacin Toxicity:gastric damage and granulocyte infiltration. [¹Ù·Î°¡±â] Replated Protein:Cytochrome b5 Drug:indomethacin Toxicity:selective effect of a p-chlorophenyl moiety. [¹Ù·Î°¡±â] Replated Protein:NADH-cytochrome b5 reductase Drug:indomethacin Toxicity:selective effect of a p-chlorophenyl moiety. [¹Ù·Î°¡±â] Replated Protein:Epoxide hydrolase Drug:indomethacin Toxicity:selective effect of a p-chlorophenyl moiety. [¹Ù·Î°¡±â]
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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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