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¼¾Å¸¸ôÁ¤75mg(µðÇǸ®´Ù¸ô) CENTERMOL TABLET 75MG[Dipyridamole]
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Àü¹®ÀǾàǰ | »èÁ¦
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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¸¸¦
ÀÌ¿ëÇÏ½Ç ¼ö ÀÖ½À´Ï´Ù.
À¯·áÁ¤º¸¸ñ·ÏÀº Àü¹®È¸¿øÀ¸·Î
·Î±×ÀÎ ÇϽøé È®ÀÎ °¡´ÉÇÕ´Ï´Ù.
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646001440[A10000981]
[º¸ÇèÄڵ忡 µû¸¥ ¾àǰ±âº»Á¤º¸ Á÷Á¢Á¶È¸]
\0 ¿ø/1Á¤(2007.11.15)(ÇöÀç¾à°¡)
\66 ¿ø/1Á¤(2003.10.01)(º¯°æÀü¾à°¡)
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µîÀû»ö ¿øÇü´çÀÇÁ¤ [Á¦ÇüÁ¤º¸ È®ÀÎ] |
| Æ÷À塤À¯Åë´ÜÀ§ |
60, 100, 500, 1000Á¤ |
| Æ÷À塤ÄÚµå´ÜÀ§ |
| ¾àǰ±Ô°Ý |
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Æ÷ÀåÇüÅ |
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Ç¥ÁØÄÚµå |
ºñ°í |
| 75¹Ð¸®±×·¥ |
100 Á¤ |
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8806460014401 |
8806460014418 |
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[Çã°¡»çÇ× ¿ø¹®Á¶È¸]
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[ÀûÀÀÁõ º° °Ë»ö]
(°æ±¸ : Á¤Á¦)
1. Çù½ÉÁõ, °ü°æÈÁõ(¸¸¼ºÇãÇ÷¼º½ÉÁúȯ, ¹«ÁõÈļºÇãÇ÷¼º½ÉÁúȯ, µ¿¸Æ°æÈ¼º½ÉÁúȯ), ½É±Ù°æ»ö(±Þ¼º±â Á¦¿Ü), ¿ïÇ÷¼º½ÉºÎÀü
2. ½ÉÀåÆÇ¸·Ä¡È¯¼úÈÄÀÇ Ç÷Àü,»öÀü ¿¹¹æÀ» À§ÇÑ Ç×ÀÀ°íÁ¦ÀÇ º¸Á¶¿ä¹ý
3. ´ÙÀ½ Áúȯ¿¡ ÀÇÇÑ ¿ä´Ü¹é°¨¼Ò : ½ºÅ×·ÎÀ̵åÀúÇ×¼º½ÅÁõÈıº
(ÁÖ»çÁ¦)
1. Çù½ÉÁõ, °ü°æÈÁõ(¸¸¼ºÇãÇ÷¼º½ÉÁúȯ, ¹«ÁõÈļºÇãÇ÷¼º½ÉÁúȯ, µ¿¸Æ°æÈ¼º½ÉÁúȯ), ½É±Ù°æ»ö, ¿ïÇ÷¼º½ÉºÎÀü
2. Å»·ý½É±Ù¿µ»óÀÇ º¸Á¶(¿îµ¿ºÎÇÏÀÇ ´ëü)
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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. Çù½ÉÁõ, °ü°æÈÁõ, ½É±Ù°æ»ö, ¿ïÇ÷¼º½ÉºÎÀü : µðÇǸ®´Ù¸ô·Î¼ 1ȸ 25-50§· 1ÀÏ 3ȸ ½Ä»ç 1½Ã°£Àü¿¡ °æ±¸Åõ¿©ÇÑ´Ù.
2. Ç÷Àü,»öÀüÁõ ¿¹¹æ : ÀÌ ¾àÀ¸·Î¼ 1ȸ 75-100§·À» 3-4ȸ Åõ¿©ÇÑ´Ù.
3. ¿ä´Ü¹é°¨¼Ò : ÀÌ ¾àÀ¸·Î¼ 1ÀÏ 300§·À» 3ȸ ºÐÇÒ Åõ¿©ÇÑ´Ù. Åõ¿©½ÃÀÛ ÈÄ 4ÁÖ°£À» ¸ñÇ¥·Î ¿ä´Ü¹é·®À» ÃøÁ¤ÇÏ¿© ¿ä´Ü¹éÀÌ °¨¼ÒµÇÁö ¾ÊÀ¸¸é Åõ¿©¸¦ ÁßÁöÇÏ°í ´Ù¸¥ ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù. ¿ä´Ü¹éÀÌ °¨¼ÒµÇ¾î °è¼Ó Åõ¿©ÇÒ °æ¿ì¿¡´Â Á¤±âÀûÀ¸·Î ¿ä´Ü¹éÀ» ÃøÁ¤ÇÑ ÈÄ Åõ¿©ÇÑ´Ù.
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1. Çù½ÉÁõ, °ü°æÈÁõ, ½É±Ù°æ»ö, ¿ïÇ÷¼º½ÉºÎÀü : µðÇǸ®´Ù¸ô·Î¼ 1ȸ 10§· 1ÀÏ 1-3ȸ õõÈ÷ Á¤¸ÆÁÖ»çÇÑ´Ù.
¼ïÀ» ¼ö¹ÝÇÏ´Â ±Þ¼º½É±Ù°æ»ö¿¡´Â ¼ïÀ» Ä¡·áÇÑ ÈÄ Åõ¿©ÇÑ´Ù.
2. Å»·ý½É±Ù¿µ»óÀÇ º¸Á¶ : ÀÌ ¾àÀ¸·Î¼ üÁß §¸´ç 0.56§·À» 4ºÐ°£¿¡ °ÉÃÄ ÃµÃµÈ÷ Á¤¸ÆÁÖ»çÇÑ´Ù. Å»·ýÀº ÀÌ ¾àÀÇ Áֻ縦 ¿ÏÀüÈ÷ ¸¶Ä¡°í 2ºÐÈÄ¿¡ ÁÖÀÔÇÑ´Ù.
¿¬·É, Áõ»ó¿¡ µû¶ó ÀûÀýÈ÷ Áõ°¨ÇÑ´Ù.
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1) ÀÌ ¾à¿¡ °ú¹ÎÁõÀÇ º´·ÂÀÌ Àִ ȯÀÚ
2) ÁßÁõÀÇ °üµ¿¸Æ½ÉÁúȯ(ºÒ¾ÈÁ¤Çü Çù½ÉÁõ, ±Þ¼º ½É±Ù°æ»ö) ȯÀÚ
3) ´ëµ¿¸ÆÆÇÇÏÇùÂøÁõ ȯÀÚ
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1) ÀÌ ¾à¿¡ °ú¹ÎÁõÀÇ º´·ÂÀÌ Àִ ȯÀÚ
2) ÁßÁõÀÇ °üµ¿¸Æ½ÉÁúȯ(ºÒ¾ÈÁ¤Çü Çù½ÉÁõ, ±Þ¼º ½É±Ù°æ»ö) ȯÀÚ
3) ÃÖ±Ù¿¡ Áö¼ÓµÈ ½É±Ù°æ»ö¿¡ ÀÇÇÑ ÀúÇ÷¾Ð ȯÀÚ
4) ÁßÁõÀÇ ÆÇ¸·Áúȯ, ´ëµ¿¸ÆÁúȯ, ´ëµ¿¸ÆÆÇÇÏÇùÂøÁõ ȯÀÚ
5) ¿ïÇ÷¼º ½ÉºÎÀü ȯÀÚ
6) ½ÉÀüµµ °á¼Õ ¹× ºÎÁ¤¸Æ ȯÀÚ(Å»·ý ½É±Ù¿µ»óÀÇ º¸Á¶¿ä¹ý¿¡ ÇÑÇÔ.)
7) ¼ïÀ̳ª ¼øÈ¯ÇãÅ»(circulatory collapse)»óÅÂÀÇ È¯ÀÚ
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1) ÀúÇ÷¾Ð ȯÀÚ
2) ½ÉÇÑ ºÒ¾ÈÁ¤¼º Çù½ÉÁõ ¶Ç´Â ÃÖ±Ù ½É±Ù°æ»öÀÌ ÀÖ¾ú´ø ȯÀÚ
3) Ç÷·ù¿ªÇÐÀû ¼öÄ¡°¡ ºÒ¾ÈÁ¤ÇÑ È¯ÀÚ(¿¹, ´ë»ó±â´ÉÀå¾Ö¼º ½ÉºÎÀü ȯÀÚ)
4) ÀÀ°íÀå¾Ö ȯÀÚ
5) ÁÂ½É½Ç ¹ÚÃâÀÌ Æó¼âµÈ ȯÀÚ
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1) ÀúÇ÷¾Ð ȯÀÚ
2) ½ÉÇÑ ºÒ¾ÈÁ¤¼º Çù½ÉÁõ ¶Ç´Â ÃÖ±Ù ½É±Ù°æ»öÀÌ ÀÖ¾ú´ø ȯÀÚ
3) Ç÷·ù¿ªÇÐÀû ¼öÄ¡°¡ ºÒ¾ÈÁ¤ÇÑ È¯ÀÚ(¿¹, ´ë»ó±â´ÉÀå¾Ö¼º ½ÉºÎÀü ȯÀÚ)
4) ÁÂ½É½Ç ¹ÚÃâÀÌ Æó¼âµÈ ȯÀÚ
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1) ¼øÈ¯±â°è : ¶§¶§·Î ¾îÁö·¯¿ò, ¿°¨, ½É°èÇ×Áø µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖ°í, µå¹°°Ô Çù½ÉÁõ µî °ü»óµ¿¸Æ ÁúȯÀÌ ¾Ç鵃 ¼ö ÀÖÀ¸¹Ç·Î ÀÌ·¯ÇÑ Áõ»óÀÌ ³ªÅ¸³ª´Â °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇÑ´Ù. ¶ÇÇÑ µå¹°°Ô ºó¸Æ, Ç÷¾Ð°ÇÏ µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
2) ¼Òȱâ°è : ¶§¶§·Î ±¸¿ª, ±¸Åä, ½Ä¿åºÎÁø, À§Àå°ü Àå¾Ö, º¹Åë, º¯ºñ, ±¸°¥, ¼³»ç, µå¹°°Ô º¹ºÎÆØ¸¸°¨ µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù .
3) °ú¹ÎÁõ : ¶§¶§·Î ÇǺιßÁø, µÎµå·¯±â, ½ÉÇÑ ±â°üÁö°æ·Ã, Ç÷°üºÎÁ¾ µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÀÌ·¯ÇÑ °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇÑ´Ù.
4) Á¤½Å½Å°æ°è : ¶§¶§·Î Çö±âÁõ, ÈïºÐ, µÎÅë, ±Çۨ, µå¹°°Ô ¸¶ºñ°¨, ¾î±ú°á¸² µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
5) ±âŸ : ¶§¶§·Î ±ÙÀ°Åë, À§È°¨(êÞûúÊï), ÈäÅë, µå¹°°Ô ¹ßÇÑ, À̸í, È«Á¶, »çÁöÀÇ µ¿Åë, ºñÃâÇ÷, ÇÇÇÏÃâÇ÷ µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
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1) ¼øÈ¯±â°è : µå¹°°Ô ÈäÅë, Çù½ÉÁõÁõ»ó µî °ü»óµ¿¸Æ ÁúȯÀÌ ¾Ç鵃 ¼ö ÀÖÀ¸¹Ç·Î ÀÌ·¯ÇÑ °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇϰųª Çʿ信 µû¶ó ¾Æ¹Ì³ëÇʸ°À» Á¤¸ÆÅõ¿©Çϸé Áõ»óÀÌ ¼Ò½ÇµÈ´Ù. ¶§¶§·Î ½É°èÇ×Áø, ÈäºÎºÒÄè°¨ µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù. ¶ÇÇÑ ÀúÇ÷¾ÐÀÌ °üÂûµÇ¾ú´Ù.
2) Á¤½Å½Å°æ°è : ¶§¶§·Î Çö±âÁõ, ¾îÁö·¯¿ò, µÎÅë, ½Ç½Å µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
3) °ú¹ÎÁõ : µå¹°°Ô ¹ßÁø µÎµå·¯±â, ½ÉÇÑ ±â°üÁö°æ·Ã, Ç÷°üºÎÁ¾µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÀÌ·¯ÇÑ °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇÑ´Ù. Á¤¸ÆÁÖ»ç½Ã ¾Æ³ªÇʶô½Ã¾ç ¹ÝÀÀÀÌ º¸°íµÇ¾ú´Ù.
4) ¼Òȱâ°è : ¶§¶§·Î ±¸¿ª, ±¸Åä, ¼³»ç µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
5) ±âŸ : ¶§¶§·Î ±ÙÀ°Åë, ¾È¸éÈ«Á¶, ¾´¸À, ¿°¨, ±Çۨ µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
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1) ÀÌ ¾àÀº ¾Æµ¥³ë½ÅÀÇ Ç÷Áß³óµµ ¹× ½ÉÇ÷°ü°è¿¡ ´ëÇÑ ÀÛ¿ëÀ» Áõ°¡½ÃŰ¹Ç·Î º´¿ëÅõ¿©½Ã ¾Æµ¥³ë½ÅÀÇ ¿ë·®À» Á¶ÀýÇØ¾ß ÇÑ´Ù.
2) ÀÌ ¾à°ú Ç×ÀÀÇ÷Á¦ ¶Ç´Â ¾Æ¼¼Æ¿ »ì¸®½Ç»êÀ» º´¿ëÅõ¿©ÇÒ ¶§´Â ¾à¹°°ú¹Î¼º ¹× À§Ç輺¿¡ ´ëÇØ °üÂûÇØ¾ß ÇÑ´Ù.
3) ÀÌ ¾àÀº °¾ÐÁ¦ÀÇ ÀúÇ÷¾Ð È¿°ú¸¦ Áõ°¡½Ãų ¼ö ÀÖ´Ù.
4) ÀÌ ¾àÀº Äݸ°¿¡½ºÅ×¶óÁ¦ ¾ïÁ¦Á¦ÀÇ Ç×Äݸ°¿¡½ºÅ×¶óÁ¦ È¿°ú¸¦ »ó¼â½ÃÄѼ ÁßÁõ ±Ù¹«·ÂÁõÀ» ¾ÇȽÃų ¼ö ÀÖ´Ù.
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1) ÀÌ ¾àÀº ¾Æµ¥³ë½ÅÀÇ Ç÷Áß³óµµ ¹× ½ÉÇ÷°ü°è¿¡ ´ëÇÑ ÀÛ¿ëÀ» Áõ°¡½ÃŰ¹Ç·Î º´¿ëÅõ¿©½Ã ¾Æµ¥³ë½ÅÀÇ ¿ë·®À» Á¶ÀýÇØ¾ß ÇÑ´Ù.
2) ÀÌ ¾à°ú Ç×ÀÀÇ÷Á¦ ¶Ç´Â ¾Æ¼¼Æ¿ »ì¸®½Ç»êÀ» º´¿ëÅõ¿©ÇÒ ¶§´Â ¾à¹°°ú¹Î¼º ¹× À§Ç輺¿¡ ´ëÇØ °üÂûÇØ¾ß ÇÑ´Ù.
3) ÀÌ ¾àÀº °¾ÐÁ¦ÀÇ ÀúÇ÷¾Ð È¿°ú¸¦ Áõ°¡½Ãų¼ö ÀÖ´Ù.
4) ÀÌ ¾àÀº Äݸ°¿¡½ºÅ×¶óÁ¦ ¾ïÁ¦Á¦ÀÇ Ç×Äݸ°¿¡½ºÅ×¶óÁ¦ È¿°ú¸¦ »ó¼â½ÃÄѼ ÁßÁõ ±Ù¹«·ÂÁõÀ» ¾ÇȽÃų ¼ö ÀÖ´Ù.
4) Ç÷°üÈ®ÀåÁ¦¿ÍÀÇ º´¿ëÅõ¿©·Î ÁßÁõÀÇ ÀúÇ÷¾ÐÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
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| Related FDA Approved Drug |
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µå·°ÀÎÆ÷ ÀǾàǰ ¿ä¾à/»ó¼¼Á¤º¸
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M050305/µðÇǸ®´Ù¸ô 75¹Ð¸®±×·¥ /
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8806460014401 |
| BIT ¾àÈ¿ºÐ·ù |
Ç×Ç÷Àü,Ç÷¼ÒÆÇÀÀÁý¾ïÁ¦Á¦ (Antithrombotics, Antiplatelet Agents)
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Dipyridamole / B01AC07
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Æû¸ñ±âÁØÄÚµå: 198300513 /´ëÇ¥ÄÚµå: 8806460014401/Ç¥ÁØÄÚµå: 8806460014418
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| Mechanism of Action |
Dipyridamole¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Dipyridamole likely inhibits both adenosine deaminase and phosphodiesterase, preventing the degradation of cAMP, an inhibitor of platelet function. This elevation in cAMP blocks the release of arachidonic acid from membrane phospholipids and reduces thromboxane A2 activity. Dipyridamole also directly stimulates the release of prostacyclin, which induces adenylate cyclase activity, thereby raising the intraplatelet concentration of cAMP and further inhibiting platelet aggregation.
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| Pharmacology |
Dipyridamole¿¡ ´ëÇÑ Pharmacology Á¤º¸ Dipyridamole, a non-nitrate coronary vasodilator that also inhibits platelet aggregation, is combined with other anticoagulant drugs, such as warfarin, to prevent thrombosis in patients with valvular or vascular disorders. Dipyridamole is also used in myocardial perfusion imaging, as an antiplatelet agent, and in combination with aspirin for stroke prophylaxis.
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| Protein Binding |
Dipyridamole¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 99%
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| Half-life |
Dipyridamole¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 40 minutes
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| Absorption |
Dipyridamole¿¡ ´ëÇÑ Absorption Á¤º¸ 70%
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| Biotransformation |
Dipyridamole¿¡ ´ëÇÑ Biotransformation Á¤º¸ hepatic
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| Toxicity |
Dipyridamole¿¡ ´ëÇÑ Toxicity Á¤º¸ Hypotension, if it occurs, is likely to be of short duration, but a vasopressor drug may be used if necessary. The oral LD50 in rats is greater than 6,000 mg/kg while in the dogs, the oral LD50 is approximately 400 mg/kg. LD50=8.4g/kg (orally in rat)
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| Drug Interactions |
Dipyridamole¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Adenosine Increases the effect/toxicity of adenosineFludarabine Decreases the effect of fludarabine
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Dipyridamole¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take with food to reduce irritation.Coffee and tea can decrease the effect of dipyridamole.
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| Drug Target |
[Drug Target]
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| Description |
Dipyridamole¿¡ ´ëÇÑ Description Á¤º¸ A phosphodiesterase inhibitor that blocks uptake and metabolism of adenosine by erythrocytes and vascular endothelial cells. Dipyridamole also potentiates the antiaggregating action of prostacyclin. (From AMA Drug Evaluations Annual, 1994, p752)
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| Drug Category |
Dipyridamole¿¡ ´ëÇÑ Drug_Category Á¤º¸ Phosphodiesterase InhibitorsPlatelet Aggregation InhibitorsVasodilator Agents
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| Smiles String Canonical |
Dipyridamole¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ OCCN(CCO)C1=NC2=C(N=C(N=C2N2CCCCC2)N(CCO)CCO)C(=N1)N1CCCCC1
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| Smiles String Isomeric |
Dipyridamole¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ OCCN(CCO)C1=NC2=C(N=C(N=C2N2CCCCC2)N(CCO)CCO)C(=N1)N1CCCCC1
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| InChI Identifier |
Dipyridamole¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C24H40N8O4/c33-15-11-31(12-16-34)23-26-20-19(21(27-23)29-7-3-1-4-8-29)25-24(32(13-17-35)14-18-36)28-22(20)30-9-5-2-6-10-30/h33-36H,1-18H2
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| Chemical IUPAC Name |
Dipyridamole¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 2-[[2-(bis(2-hydroxyethyl)amino)-4,8-di(piperidin-1-yl)pyrimido[6,5-e]pyrimidin-6-yl]-(2-hydroxyethyl)amino]ethanol
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