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ÀϾç¸ÞÅç¶óÁ¸Á¤(¸ÞÅç¶óÁ¸) METOLAZON TAB. ILYANG[Metolazone]
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µå·°ÀÎÆ÷¿¡¼´Â ÀǾàǰ ÀÎÅÍ³Ý ÆÇ¸Å¸¦ ÇÏÁö ¾Ê½À´Ï´Ù. |
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À¯·áȸ¿ø °áÀç½Ã¿¡´Â º¸´Ù ´Ù¾çÇÑ ¾à¹°Á¤º¸¸¦
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À¯·áÁ¤º¸¸ñ·ÏÀº Àü¹®È¸¿øÀ¸·Î
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641701670[A09553791]
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1. ¿ïÇ÷½ÉºÎÀü¿¡ µû¸¥ ºÎÁ¾
2. ½ÅÁõÈıº ¹× ½Å±â´ÉÀÌ ÀúÇÏµÈ »óŸ¦ Æ÷ÇÔÇÏ´Â ½ÅÀåÁúȯ¿¡ µû¸¥ ºÎÁ¾
3. °æÁõ¿¡¼ Áߵ º»Å°íÇ÷¾Ð
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* Àý´ë ÀÓÀǺ¹¿ëÇÏÁö ¸¶½Ã°í ¹Ýµå½Ã ÀÇ»ç ¶Ç´Â ¾à»ç¿Í »ó´ãÇϽñ⠹ٶø´Ï´Ù.
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1. ¿ïÇ÷½ÉºÎÀü¿¡ µû¸¥ ºÎÁ¾ : ¸ÞÅç¶óÁ¸À¸·Î¼ 1ÀÏ 1ȸ 5 ¢¦ 10 mgÀ» °æ±¸Åõ¿©ÇÑ´Ù.
2. ½ÅÀåÁúȯ¿¡ µû¸¥ ºÎÁ¾ : ÀÌ ¾àÀ¸·Î¼ 1ÀÏ 1ȸ 5 ¢¦ 20 mgÀ» °æ±¸Åõ¿©ÇÑ´Ù.
3. °æÁõ¿¡¼ Áߵ º»Å°íÇ÷¾Ð : ÀÌ ¾àÀ¸·Î¼ 1ÀÏ 1ȸ 2.5 ¢¦ 5 mgÀ» °æ±¸Åõ¿©ÇÑ´Ù.
Áõ»ó¿¡ µû¶ó ÀûÀýÈ÷ Áõ°¨ÇÑ´Ù.
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Ãʱâ¿ë·®ÀÇ È¿°ú°¡ ³ªÅ¸³ª´Âµ¥ ÇÊ¿äÇÑ ½Ã°£°£°ÝÀº ´Ù¾çÇÒ ¼ö ÀÖ´Ù. ÀÌ´¢ ¹× ¿°ºÐ¹è¼³Àº º¸Åë 1½Ã°£ À̳»¿¡ ³ªÅ¸³ª¸ç, 24½Ã°£ ¶Ç´Â ±× ÀÌ»ó µ¿¾È Áö¼ÓµÈ´Ù. ¿øÇÏ´Â Ä¡·áÈ¿°ú¸¦ ¾ò¾úÀ» °æ¿ì, °¡´ÉÇÏ¸é ¿ë·®À» ÁÙÀÌ´Â °ÍÀÌ ¹Ù¶÷Á÷ÇÏ´Ù. 1ÀÏ ¿ë·®Àº ȯÀÚÀÇ »óÅÂ, ³ªÆ®·ýÀÇ ¼·Ãë, ¹ÝÀÀÀÇ Á¤µµ¿¡ ´Þ·Á ÀÖ´Ù. 1ÀÏ ¿ë·® º¯°æÀº öÀúÇÑ ÀÓ»óÀû, ½ÇÇèÀû Æò°¡ °á°ú¿¡ ±Ù°ÅÇÏ¿©¾ß ÇÑ´Ù. ÀÌ ¾à°ú Ç÷¾Ð°ÇÏÁ¦ ¶Ç´Â ÀÌ´¢Á¦¿Í º´¿ëÇÒ °æ¿ì, ´õ ÁÖÀÇ ±íÀº ¿ë·®Á¶ÀýÀÌ ÇÊ¿äÇÏ´Ù. ¹ßÀ۾߰£È£Èí°ï¶õÀ» °æÇèÇÑ È¯Àڵ鿡°Ô 24½Ã°£µ¿¾È ÀÌ´¢ ¹× ¿°ºÐ¹è¼³À» Áö¼Ó½Ã۱â À§ÇØ ¿ë·®¹üÀ§ Áß ³ôÀº ¿ë·®À» Åõ¿©ÇÏ´Â °ÍÀÌ ¹Ù¶÷Á÷ÇÒ ¼ö ÀÖ´Ù.
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1) ÀüÇØÁú °áÇÌ »óÅ ¶Ç´Â ¹«´¢ ȯÀÚ
2) °£¼º È¥¼ö ¶Ç´Â È¥¼öÀü »óÅÂ
3) ÀÌ ¾à ¹× ÀÌ ¾àÀÇ ±¸¼º¼ººÐ¿¡ ¾Ë·¹¸£±â³ª °ú¹Î¹ÝÀÀÀÌ Àִ ȯÀÚ
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1) ÁßÁõ °£Áúȯ ȯÀÚ
2) ÁßÁõ ½Å±â´É¼Õ»ó ȯÀÚ
3) °í·ÉÀÚ
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ÀÌ ¾àÀº ÀϹÝÀûÀ¸·Î ³»¾à¼ºÀÌ ÁÁÀ¸¸ç, º¸°íµÈ ´ëºÎºÐÀÇ ÀÌ»ó¹ÝÀÀÀº °æ¹ÌÇϰí ÀϽÃÀûÀ̾ú´Ù. ÀÌ ¾à°ú ¿¬°üµÈ ¸¹Àº ÀÌ»ó¹ÝÀÀµéÀº ¿¹»óµÇ´Â ¾à¸®ÀÛ¿ëÀÇ È®´ëÀ̸ç, ÀÌ ¾àÀÇ Ç÷¾Ð°ÇÏÈ¿°ú´Â ½ÅÀå ¹× ´ë»çÀÛ¿ë¿¡ ÀÇÇØ ±âÀÎÇÒ ¼ö ÀÖ´Ù. ´ÙÀ½°ú °°Àº ÀÌ»ó¹ÝÀÀ Áß ¸î¸îÀº ´Üȸ ¶Ç´Â °ÅÀÇ µå¹°°Ô ÀϾ ¼ö ÀÖ´Ù. ½Åüº° ÀÌ»ó¹ÝÀÀÀº ÁßÁõµµ °¨¼Ò¼øÀ¸·Î ³ª¿ÇÏ¿´´Ù.
1) ½ÉÇ÷°ü°è : ÈäºÎÅëÁõ/ºÒÄè°¨, ±â¸³ÀúÇ÷¾Ð, °úµµÇÑ Ã¼¾× °í°¥, Ç÷¾×³óÃà, Á¤¸ÆÇ÷Àü, ½É°èÇ×Áø
2) ÁßÃß ¹× ¸»ÃʽŰæ°è : ½Ç½Å, ½Å°æº´Áõ, À̻󰨰¢, Á¤½Å°úÀû ¿ì¿ïÁõ, ¹ß±âºÎÀü, ¾îÁö·³, °¡º¿î µÎÅë, Á¹À½, ÇÇ·Î, ¼è¾à, µé¶ä(¶§¶§·Î ºÒ¸é ¾ß±â), µÎÅë
3) °ú¹Î¹ÝÀÀ : ±«»ç¼º Ç÷°ü¿°(ÇǺÎÀÇ Ç÷°ü¿°), ÀÚ»ö¹Ýº´, ÇǺο°(±¤¹Î°¨¹ÝÀÀ), µÎµå·¯±â, ÇǺιßÁø
4) ¼Òȱâ°è : °£¿°, °£³» ´ãÁó¿ïü¼º Ȳ´Þ, ÃéÀå¿°, ±¸Åä, ±¸¿ª, »óº¹ºÎºÒÄè°¨, ¼³»ç, º¯ºñ, ½Ä¿åºÎÁø, º¹ºÎÆØ¸¸
5) Ç÷¾×°è : Àç»ýºÒ·®¼º/ÀúÇü¼º¼º ºóÇ÷, ¹«°ú¸³±¸Áõ, ¹éÇ÷±¸°¨¼ÒÁõ
6) ´ë»ç : ÀúÄ®·ýÇ÷Áõ, Àú³ªÆ®·ýÇ÷Áõ, °í¿ä»êÇ÷Áõ, Àú¿°¼ÒÇ÷Áõ, Àú¿°¼ÒÇ÷Áõ¼º ¾ËÄ®¸®Áõ, °íÇ÷´çÁõ, ´ç´¢, Ç÷û¿ä¼ÒÁú¼Ò»ó½Â ¶Ç´Â Å©·¹¾ÆÆ¼´Ñ »ó½Â, ÀúÀÎÇ÷Áõ, Àú¸¶±×³×½·Ç÷Áõ, °íÄ®½·Ç÷Áõ
7) ±Ù°ñ°Ý°è : °üÀýÅë, ±Þ¼º Åëdz ¹ßÀÛ, ±Ù°æ·Ã, °æÃà
8) ±âŸ : ÀϽÃÀû ½Ã¾ßÈ帲, ¿ÀÇÑ
¶ÇÇÑ À¯»çÇÑ Ç×°íÇ÷¾Ð¼º ÀÌ´¢Á¦¿¡¼´Â º¸°íµÇ¾úÀ¸³ª, ÀÌ ¾à¿¡¼´Â º¸°íµÇÁö ¾ÊÀº ÀÌ»ó¹ÝÀÀÀº ´ÙÀ½°ú °°´Ù.
¾´¸À, ±¸°¥, Ÿ¾×¼±¿°, Ȳ»ö½ÃÁõ, È£Èí±â°ï¶õ(Æó·ÅÆ÷ÇÔ), Ç÷¼ÒÆÇ°¨¼ÒÁõ, ¾Æ³ªÇʶô½Ã½º¹ÝÀÀ, ÀÌ ¾àÀÇ ÀÓ»óÀû »ç¿ë¿¡¼µµ À§ÀÇ ÀÌ»ó¹ÝÀÀÀÌ ÀÏ¾î ³¯ ¼ö ÀÖÀ½À» °í·ÁÇØ¾ß ÇÑ´Ù. ÀÌ»ó¹ÝÀÀµéÀÌ ÁßÁõµµ ¶Ç´Â ÁßÁõÀÏ °æ¿ì¿¡´Â °¨·®Çϰųª Ä¡·á¸¦ Áß´ÜÇØ¾ß ÇÑ´Ù.
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1) ÀÌ´¢Á¦ : Ǫ·Î¼¼¹Ìµå ¹× ´Ù¸¥ ·çÇÁ°è ÀÌ´¢Á¦¿Í ÀÌ ¾àÀ» º´¿ëÇÒ °æ¿ì ºñÁ¤»óÀûÀ¸·Î ü¾×°ú ÀüÇØÁúÀÇ °ú·® ¶Ç´Â Áö¼ÓÀûÀÎ ¼Õ½ÇÀ» ÃÊ·¡ÇÒ ¼ö ÀÖ´Ù.
2) ´Ù¸¥ Ç÷¾Ð°ÇÏÁ¦ : ´Ù¸¥ Ç÷¾Ð°ÇÏÁ¦¿Í º´¿ëÇÒ °æ¿ì, ƯÈ÷ Ãʱâ Ä¡·á±â°£¿¡´Â ÁÖÀÇÇØ¾ß ÇÑ´Ù(ÀÌ ¾à°ú ´Ù¸¥ ºñÀÌ´¢¼º Ç÷¾Ð°ÇÏÁ¦¸¦ º´¿ëÇÒ °æ¿ì, Ãʱâ Ä¡·á½Ã °úµµÇÑ Ç÷¾ÐÀúÇϸ¦ ÇÇÇϵµ·Ï ÁÖÀÇÇØ¾ß ÇÑ´Ù.). ´Ù¸¥ Ç÷¾Ð°ÇÏÁ¦ÀÇ ¿ë·®ÀûÁ¤ÀÌ ÇÊ¿äÇÒ ¼ö ÀÖ´Ù.
3) ¾ËÄÚ¿Ã, ¹Ù¸£ºñÅ»°è ¾à¹°, ¸¶¾à·ù : ¸ÞÅç¶óÁ¸ Åõ¿©¿Í ¿¬°üµÈ ¿ë·® °¨¼Ò¿¡ ÀÇÇØ ÀÌµé ¾à¹°ÀÇ Ç÷¾ÐÀúÇÏÈ¿°ú°¡ °È µÉ ¼ö ÀÖ´Ù.
4) µð±âÅ»¸®½º ¹è´çü : ÀÌ´¢Á¦¿¡ ÀÇÇÑ ÀúÄ®·ýÇ÷ÁõÀÌ µð±âÅ»¸®½º¿¡ ´ëÇÑ ½É±ÙÀÇ °¨¼ö¼ºÀ» Áõ°¡½Ãų ¼ö ÀÖ´Ù.
5) ÄÚ¸£Æ¼ÄÚ½ºÅ×·ÎÀÌµå ¶Ç´Â ACTH : ÀúÄ®·ýÇ÷ÁõÀÇ À§Ç輺°ú ¿°ºÐ ¹× ¼öºÐ Àú·ù¸¦ Áõ°¡½Ãų ¼ö ÀÖ´Ù.
6) ¸®Æ¬ : Ç÷û ¸®Æ¬³óµµ°¡ Áõ°¡µÉ ¼ö ÀÖ´Ù. ÀÌ´¢Á¦´Â ¸®Æ¬ÀÇ ½Åû¼ÒÀ²À» °¨¼Ò½Ã۰í, ¸®Æ¬µ¶¼ºÀ» Áõ°¡½ÃŰ¹Ç·Î ÀϹÝÀûÀ¸·Î ÀÌ´¢Á¦¿Í ¸®Æ¬Àº º´¿ëÇÏÁö ¾Ê´Â´Ù. ÀÌ·± º´¿ëÄ¡·áÀü¿¡´Â ¸®Æ¬Á¦Á¦¿¡ ´ëÇÑ ¼³¸í¼¸¦ Àо °Í.
7) CurareÇü ¾à¹° : ÀÌ´¢Á¦·Î À¯µµµÈ ÀúÄ®·ýÇ÷ÁõÀº curareÇü ¾à¹°(¿¹, Åõº¸Äí¶ó¸°)ÀÇ ½Å°æ±Ù Â÷´ÜÀÛ¿ëÀ» Áõ°½Ãų ¼ö ÀÖ´Ù. °¡Àå ½É°¢ÇÑ ÀÌ»ó¹ÝÀÀÀº ¹«È£ÈíÀ¸·Î ÁøÇàµÉ ¼ö Àִ ȣÈí±â¾ïÁ¦ÀÌ´Ù. ±×·¯¹Ç·Î ¼ö¼ú 3ÀÏÀü¿¡´Â ÀÌ ¾à Åõ¿©¸¦ Áß´ÜÇÏ´Â °ÍÀÌ ±ÇÀåµÈ´Ù.
8) Salicylates ¹× ´Ù¸¥ ºñ½ºÅ×·ÎÀ̵å¼Ò¿°ÁøÅëÁ¦(NSAID) : ÀÌ ¾àÀÇ Ç×°íÇ÷¾ÐÈ¿°ú¸¦ °¨¼Ò½Ãų ¼ö ÀÖÀ¸¹Ç·Î ÁÖÀÇ ±íÀº ¸ð´ÏÅ͸µÀÌ ÇÊ¿äÇÏ´Ù.
9) ±³°¨½Å°æÈïºÐ¾à : ÀÌ ¾àÀº ³ë¸£¿¡Çdz×ÇÁ¸°¿¡ ´ëÇÑ µ¿¸ÆÀÇ ¹ÝÀÀ¼ºÀ» °¨¼Ò½Ãų ¼ö ÀÖÀ¸³ª, ÀÌ·± °¨¼ÒÁ¤µµ°¡ Ä¡·á¸ñÀûÀÇ ½Â¾Ð¾à È¿°ú¸¦ ¹èÁ¦Çϱ⿡´Â ÃæºÐÇÏÁö ¾Ê´Ù.
10) Àν¶¸° ¹× °æ±¸ ´ç´¢º´¿ëÁ¦ : ¿ë·®Á¶ÀýÀÌ ÇÊ¿äÇÒ ¼ö ÀÖ´Ù(ÀϹÝÀû ÁÖÀÇÇ×ÀÇ '´ç³»¼º'ÂüÁ¶).
11) ¸ÞÅ׳ª¹Î : ÀÌ ¾àÀÇ ¿ä ¾ËÄ®¸®È È¿°ú¿¡ ÀÇÇØ ¸ÞÅ׳ª¹ÎÀÇ È¿°ú°¡ ¶³¾îÁú ¼ö ÀÖ´Ù.
12) Ç×ÀÀ°íÁ¦ : ´Ù¸¥ Ƽ¾ÆÁöµå°è ÀÌ´¢Á¦¿Í ¸¶Âù°¡Áö·Î ÀÌ ¾àÀº Ç×ÀÀ°íÁ¦¿¡ ÀÇÇÑ ÀúÇÁ·ÎÆ®·Òºó¹ÝÀÀ¿¡ ¿µÇâÀ» ¹ÌÄ¥ ¼ö ÀÖÀ¸¹Ç·Î ¿ë·® Á¶ÀýÀÌ ÇÊ¿äÇÒ ¼ö ÀÖ´Ù.
13) Åëdzġ·á ¾à¹° : °í¿ä»êÇ÷Áõ°ú ÅëdzÀ» Á¶ÀýÇϱâ À§ÇØ Åëdz ¾à¹°ÀÇ ¿ë·®Á¶ÀýÀÌ ÇÊ¿äÇÒ ¼ö ÀÖ´Ù.
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°í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
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| Mechanism of Action |
Metolazone¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ The actions of metolazone result from interference with the renal tubular mechanism of electrolyte reabsorption. Metolazone acts primarily to inhibit sodium reabsorption at the cortical diluting site and to a lesser extent in the proximal convoluted tubule. Sodium and chloride ions are excreted in approximately equivalent amounts. The increased delivery of sodium to the distal tubular exchange site results in increased potassium excretion. Metolazone does not inhibit carbonic anhydrase. The antihypertensive mechanism of action of metolazone is not fully understood but is presumed to be related to its saluretic and diuretic properties.
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| Pharmacology |
Metolazone¿¡ ´ëÇÑ Pharmacology Á¤º¸ Metolazone is a quinazoline diuretic, with properties generally similar to the thiazide diuretics. A proximal action of metolazone has been shown in humans by increased excretion of phosphate and magnesium ions and by a markedly increased fractional excretion of sodium in patients with severely compromised glomerular filtration. This action has been demonstrated in animals by micropuncture studies.
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| Protein Binding |
Metolazone¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Dose dependent.
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| Half-life |
Metolazone¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ Approximately 14 hours.
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| Absorption |
Metolazone¿¡ ´ëÇÑ Absorption Á¤º¸ Peak blood levels are obtained within 2 to 4 hours of oral administration.
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| Pharmacokinetics |
MetolazoneÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- ¸ðµç Åõ¿©°æ·Î¿¡¼ µ¿ÀÏ
- ÀÌ´¢È¿°ú ¹ßÇö½Ã°£ : 60ºÐ À̳»
- ÀÛ¿ë¹ßÇö½Ã°£ : 12-24½Ã°£
- Èí¼ö : °æ±¸ : ºÒ¿ÏÀüÇÏ´Ù.
- ºÐÆ÷ : ŹÝÀ» Åë°úÇÑ´Ù. À¯Áó¿¡¼µµ °ËÃâµÈ´Ù.
- ´Ü¹é°áÇÕ : 95%
- ¹Ý°¨±â : 6-20½Ã°£(½Å±â´É ÀÇÁ¸Àû)
- ¼Ò½Ç : Àå°£¼øÈ¯(enterohepatic recycling), 80-95%°¡ ½Å¹è¼³µÈ´Ù.
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| Toxicity |
Metolazone¿¡ ´ëÇÑ Toxicity Á¤º¸ Symptoms of overdose include difficulty breathing, dizziness, dizziness on standing up, drowsiness, fainting, irritation of the stomach and intestines, and lethargy leading to coma.
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| Drug Interactions |
Metolazone¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Amantadine The diuretic increases the adverse effects of amantadineDeslanoside Possible electrolyte variations and arrhythmiasDigitoxin Possible electrolyte variations and arrhythmiasDigoxin Possible electrolyte variations and arrhythmiasDofetilide Increased risk of cardiotoxicity and arrhythmiasLithium The thiazide diuretic increases serum levels of lithium
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Metolazone¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take with food to reduce gastric irritation.
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| Drug Target |
[Drug Target]
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| Description |
Metolazone¿¡ ´ëÇÑ Description Á¤º¸ A quinazoline-sulfonamide that is considered a thiazide-like diuretic which is long-acting so useful in chronic renal failure. It also tends to lower blood pressure and increase potassium loss. [PubChem]
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| Drug Category |
Metolazone¿¡ ´ëÇÑ Drug_Category Á¤º¸ Antihypertensive AgentsDiureticsDiuretics, Sulfamyl
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| Smiles String Canonical |
Metolazone¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC1NC2=CC(Cl)=C(C=C2C(=O)N1C1=CC=CC=C1C)S(N)(=O)=O
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| Smiles String Isomeric |
Metolazone¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ C[C@@H]1NC2=CC(Cl)=C(C=C2C(=O)N1C1=CC=CC=C1C)S(N)(=O)=O
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| InChI Identifier |
Metolazone¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C16H16ClN3O3S/c1-9-5-3-4-6-14(9)20-10(2)19-13-8-12(17)15(24(18,22)23)7-11(13)16(20)21/h3-8,10,19H,1-2H3,(H2,18,22,23)/f/h18H2
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| Chemical IUPAC Name |
Metolazone¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 7-chloro-2-methyl-3-(2-methylphenyl)-4-oxo-1,2-dihydroquinazoline-6-sulfonamide
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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