|
|
|
|
|
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.
|
|
|
 | Çã°¡Á¤º¸ |
|
|
| Ç׸ñ |
³»¿ë |
û±¸ÄÚµå(KDÄÚµå) ºñ±Þ¿©Á¡°ËÄÚµå »óÇÑ±Ý¾× |
641703530[A09500961]
[º¸ÇèÄڵ忡 µû¸¥ ¾àǰ±âº»Á¤º¸ Á÷Á¢Á¶È¸]
\0 ¿ø/1Á¤(2007.03.01)(ÇöÀç¾à°¡)
\43 ¿ø/1Á¤(2002.07.12)(º¯°æÀü¾à°¡)
[»óº´ÄÚµåÁ¶È¸]
[Áúº´ÄÚµåÁ¶È¸]
|
| ºü¸¥Á¶È¸ |
|
| Á¦Ç°¼º»ó |
Çʸ²ÄÚÆÃÀ» ÇÑ È²»öÀÇ Á¤Á¦ [Á¦ÇüÁ¤º¸ È®ÀÎ] |
| Æ÷À塤À¯Åë´ÜÀ§ |
100,300,500,1000TABS |
| È¿´ÉÈ¿°ú |
[ÀûÀÀÁõ º° °Ë»ö]
È¿´É È¿°ú
(°æ±¸ : Á¤Á¦)
°íÇ÷¾Ð(º»Å¼º, ½Å¼ºµî)
|
| ¿ë¹ý¿ë·® |
* Àý´ë ÀÓÀǺ¹¿ëÇÏÁö ¸¶½Ã°í ¹Ýµå½Ã ÀÇ»ç ¶Ç´Â ¾à»ç¿Í »ó´ãÇϽñ⠹ٶø´Ï´Ù.
[󹿾à¾î]
¿ë¹ý¿ë·®
(°æ±¸ : Á¤Á¦)
¼ºÀÎ : ¸ÞÄ¥µµÆÄ·Î¼ ÃÊȸ·®À¸·Î 1ȸ 250§· 1ÀÏ 2-3ȸ °æ±¸Åõ¿©Çϸç ÀûÀýÇÑ Ç÷¾Ð°ÇÏÈ¿°ú°¡ ³ªÅ¸³¯ ¶§±îÁö 2ÀÏ ÀÌ»óÀǰ£°ÝÀ» µÎ°í 1ÀÏ 250§·¾¿ Áõ·®ÇÑ´Ù. À¯Áö·®À¸·Î 1ÀÏ 500-2000§·À» 2-4ȸ ºÐÇÒÅõ¿©ÇÑ´Ù.
¿¬·É, Áõ»ó¿¡ µû¶ó ÀûÀýÈ÷ Áõ°¨ÇÑ´Ù.
|
| ÁÖ¿ä¾à¹° »óÈ£ÀÛ¿ë |
[Á¶È¸]
|
| ±Ý±â |
1) ±Þ¼º °£Áúȯ ȯÀÚ(±Þ¼º°£¿°, Ȱµ¿±â °£°æº¯ µî)
2) ÁßÁõÀÇ ½Å±â´ÉÀå¾Ö ȯÀÚ
3) Å©·Òģȼ¼Æ÷Á¾ ȯÀÚ
4) ¿ëÇ÷¼º ºóÇ÷ ȯÀÚ
5) ¿ì¿ïÁõ ȯÀÚ
6) ÀÌ ¾à¿¡ ÀÇÇÑ °£ÁúȯÀÇ º´·ÂÀÌ Àִ ȯÀÚ
7) ÀÌ ¾à¿¡ °ú¹ÎÁõÀÇ º´·ÂÀÌ Àִ ȯÀÚ
|
| ½ÅÁßÅõ¿© |
1) °£Áúȯ º´·Â ¶Ç´Â °£±â´ÉÀå¾ÖȯÀÚ
2) °í·ÉÀÚ
3) °£¼º Æ÷¸£ÇǸ° ¹× ±× °¡Á··ÂÀÌ Àִ ȯÀÚ
|
| ÀÌ»ó¹ÝÀÀ |
1) ¹ß¿ ¹× °£Àå : ¶§¶§·Î È£»ê±¸Áõ°¡, °£±â´ÉÀå¾Ö¿¡ ÀÇÇÑ ¹ß¿(Åõ¿©Ãʱâ 3ÁÖ À̳»¿¡ ¸¹ÀÌ ³ªÅ¸³´Ù),µå¹°°Ô ¹ß¿ÇÏÁö ¾Ê´Â Ȳ´Þ, °£¿°Áõ»ó(Åõ¿©Ãʱâ 3°³¿ù À̳»¿¡ ¸¹ÀÌ ³ªÅ¸³´Ù)ÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ¿øÀκҸíÀÇ ¹ß¿, °£±â´ÉÀÌ»ó µîÀÌ ÀÎÁ¤µÉ °æ¿ì¿¡´Â Áï½Ã Åõ¿©¸¦ ÁßÁöÇϰí ÀçÅõ¿©ÇÏÁö ¾Ê´Â´Ù. ¶ÇÇÑÅõ¿©Ãʱ⿡´Â Á¤±âÀûÀ¸·Î °£±â´É°Ë»ç ¹× ¹éÇ÷±¸ ºÐȹ°Ë»ç¸¦ ÇÑ´Ù.
2) Ç÷¾× : µå¹°°Ô ¿ëÇ÷¼º ºóÇ÷, ¹éÇ÷±¸°¨¼Ò,¹«°ú¸³±¸Áõ ¹× Ç÷¼ÒÆÇ°¨¼Ò µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ºóÇ÷ÀÌ ³ªÅ¸³¯ °æ¿ì¿¡´Â Áï½Ã Åõ¿©¸¦ ÁßÁöÇÑ´Ù.
3) Á¤½Å½Å°æ°è : ¹«·Â°¨, ¶§¶§·Î µÎÅë, Á¹À½, ¾îÁö·¯¿ò, ´Ù¸®°¡ Èĵé°Å¸², ³úÇ÷°üºÎÀüÁõ»ó, °¨°¢ÀÌ»ó, µå¹°°Ô ¿ì¿ï, Á¤½ÅȰµ¿°¨Åð, ¾Ç¸ù, ºÒ¸é, ÆÄŲ½¼ÁõÈıº, ÁßÁõÀÇ ¾çÃø¼º ³úÇ÷°üÀå¾Ö ȯÀÚ¿¡¼ÀÇ ¹«µµº´ ¾ÆÅ×Åä½Ã½º¼º ¿îµ¿, ¾çÃø¼ºº§¸¶ºñ µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
4) ¼øÈ¯±â°è : ¿ïÇ÷¼º ½ÉºÎÀü ¶§¶§·Î ¼¸Æ, ±â¸³¼º ÀúÇ÷¾Ð, µå¹°°Ô Çù½ÉÁõ ¹ßÀÛ À¯¹ß, °æµ¿¸Æµ¿ÀÇ °ú¹ÎÁõ»ó¿¡ ÀÇÇÑ ¼¸Æ, ½Ç½Å µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÀÌ·¯ÇÑ °æ¿ì¿¡´Â °¨·® µî ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù.
5) ¼Òȱâ°è : ±¸°°ÇÁ¶ ¶§¶§·Î ±¸¿ª, ±¸Åä, ½Ä¿åºÎÁø, ±¸°¥, ¼³»ç, º¯ºñ, º¹ºÎÆØ¸¸ ¶Ç´Â µå¹°°Ô ´ëÀå¿°, Çô°¡ °ÅÄ¥¾îÁö°Å³ª °Ë°Ô µÇ°í Ÿ¾×¼±¿°, ÃéÀå¿° µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
6) ºñ´¢»ý½Ä±â°è : ¶§¶§·Î¼º¿å°¨Åð, ¹ß±âºÎÀü µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
7) °ú¹ÎÁõ : Ç÷°ü¿°, Ãæ¼öÁÖÀ§¿° µå¹°°Ô ¹ßÁø(ż±¾ç¹ßÁø, ½ÀÁø µî), ½É±Ù¿°, ½É³¶¿°µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÀÌ·¯ÇÑ °æ¿ì´Â Åõ¿©¸¦ ÁßÁöÇÑ´Ù.
8) Àü½Å¼º È«¹Ý¼º ·çǪ½º(SLE) Áõ»ó : µå¹°°Ô Àü½Å¼º È«¹Ý¼º ·çǪ½º(SLE) Áõ»ó[°üÀýÅë, ·¹À̳ëÇö»ó, Ç×ÇÙÇ×ü(ANA),LE¼¼Æ÷,·ù¸¶ÅäÀ̵åÀÎÀھ缺]ÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î °üÂûÀ» ÃæºÐÈ÷ Çϰí ÀÌ·¯ÇÑ Áõ»óÀÌ ³ªÅ¸³ª´Â °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇÑ´Ù.
9) ±âŸ : ¶§¶§·Î ÄÚ¸·Èû, üÁßÁõ°¡, ºÎÁ¾, µå¹°°Ô ±ÙÀ°Åë, °üÀýÅë, ¿©¼ºÇüÀ¯¹æ, À¯¹æºñ´ë, À¯ÁóºÐºñ, ¹«¿ù°æ, °íÇÁ·Î¶ôƾÇ÷Áõ, BUN»ó½Â, Ȳ´ÞÀ̳ªÅ¸³¯ ¼ö ÀÖ´Ù.
|
| »óÈ£ÀÛ¿ë |
1) ¸¶ÃëÁ¦¿¡ ÀÇÇØ ÀÌ ¾àÀÇ ÀÛ¿ëÀÌ Áõ°¡µÇ¾îÀúÇ÷¾ÐÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÀÌ ¾àÀ» Åõ¿©¹Þ°í Àִ ȯÀÚ¿¡´Â ¸¶ÃëÁ¦¸¦ °¨·®ÇÏ´Â µî ÁÖÀÇÇÑ´Ù. ÀÌ ÀúÇ÷¾ÐÀºº¸Åë Ç÷¾Ð»ó½ÂÁ¦ÀÇ Åõ¿©·Î ȸº¹µÈ´Ù.
2) ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°ÁøÅëÁ¦, ÄÚ¸£Æ¼ÄÚÀ̵å¿Í º´¿ëÅõ¿©ÇÏ´Â °æ¿ì¿¡´Â ³ªÆ®·ýÀÇ Àú·ù·Î Ç÷¾Ð°ÇÏÀÛ¿ëÀÌ °¨¼ÒµÉ ¼ö ÀÖ´Ù.
3) ½ÅÀåÀ» ÅëÇÑ ¸®Æ¬¹è¼³ÀÌ °¨¼ÒµÇ¾î¸®Æ¬¿¡ ÀÇÇÑ ½Éµ¶¼º ¹× ½Å°æµ¶¼ºÀÌ Áõ°¡µÉ ¼ö ÀÖÀ¸¹Ç·Î ½ÅÁßÈ÷ ¸ð´ÏÅÍÇÏ°í ¿ë·®À» Á¶ÀýÇÑ´Ù.
4) ö°ú º´¿ëÅõ¿©ÇÏ´Â °æ¿ì¿¡´Â ÀÌ ¾àÀÇÈí¼ö°¡ ÀúÇØµÉ ¼ö ÀÖ´Ù.
5) »ïȯ°è Ç׿ì¿ïÁ¦, ¹Ù¸£ºñÅ»°è ¾à¹°, ±³°¨½Å°æÈ¿´É¾à,MAOÀúÇØÁ¦¿Í º´¿ëÅõ¿©ÇÏ´Â °æ¿ì¿¡´Â ÀÌ ¾àÀÇ Ç÷¾Ð°ÇÏÀÛ¿ëÀÌ °¨¼ÒµÉ ¼ö ÀÖ´Ù.
6) ÁßÃ߽Űæ¾ïÁ¦Á¦, ¾ËÄڿõî°ú º´¿ëÅõ¿©ÇÏ´Â °æ¿ì¿¡´Â ÁßÃß¾ïÁ¦ÀÛ¿ëÀÌ Áõ°¡µÉ ¼ö ÀÖ´Ù.
7) ·¹º¸µµÆÄ, ¹ÙŬ·ÎÆæ µî°ú º´¿ëÅõ¿©ÇÏ´Â °æ¿ì¿¡´Â Ç÷¾Ð°ÇÏÀÛ¿ëÀÌ Áõ°¡µÉ ¼ö ÀÖÀ¸¹Ç·Î ÁÖÀÇÇÑ´Ù.
8) ´Ù¸¥ Ç÷¾Ð°ÇÏÁ¦¸¦ Åõ¿©¹Þ°í ÀÖ´ÂȯÀÚ¿¡°Ô ÀÌ ¾àÀ» º´¿ëÅõ¿©ÇÏ´Â °æ¿ì¿¡´Â Ç÷¾Ð°ÇÏÀÛ¿ëÀ» Áõ°¡½Ãų ¼ö ÀÖÀ¸¹Ç·Î Ç÷¾Ð°ÇÏÁ¦ÀÇ ¿ë·®Á¶Àýµî¿¡ ÁÖÀÇÇÑ´Ù.
|
| Related FDA Approved Drug |
|
|
|
 | Á¤º¸¿ä¾à |
|
|
|
µå·°ÀÎÆ÷ ÀǾàǰ ¿ä¾à/»ó¼¼Á¤º¸
|
|
 | ÄÚµå ¹× ºÐ·ùÁ¤º¸ |
|
|
| |
|
 | Á¦Ç°Á¤º¸ |
|
|
|
|
 | º¹¾àÁ¤º¸ |
|
|
| Ç׸ñ |
³»¿ë |
| LACTmed ¹Ù·Î°¡±â |
[¹Ù·Î°¡±â]
|
| ¾à¸®ÀÛ¿ë |
À¯·áÁ¤º¸ÀÔ´Ï´Ù.
|
| º¹¾àÁöµµ |
À¯·áÁ¤º¸ÀÔ´Ï´Ù.
|
| ÀӺο¡´ëÇÑÅõ¿© |
| * |
ÀüüÀӽŠ±â°£º°·Î ¿©·¯µî±ÞÀÌ Á¸ÀçÇÒ ¼ö ÀÖÀ¸¸ç °¡Àå À§Çèµµ°¡ ³ôÀº Á¤º¸¸¸ º¸¿©Áý´Ï´Ù. ´Ü, º¹ÇÕÁ¦ÀÇ °æ¿ì ¸ðµç º¹ÇÕÁ¦¼ººÐ¿¡ ´ëÇÑ ÀÓºÎÅõ¿©µî±ÞÀÌ Ç¥½ÃµÈ°ÍÀº Àý´ë ¾Æ´Ï¸ç Ç¥½ÃµÈ°ÍÁß¿¡ °¡Àå À§Çèµµ°¡ ³ôÀº Á¤º¸¸¸ ³ªÅ¸³³´Ï´Ù.
|
|
|   |
 FDA : Bµî±Þ
|
|
| * |
»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.
|
| * |
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.
|
|
|
| Pharmacokinetics |
À¯·áÁ¤º¸ÀÔ´Ï´Ù.
|
| º´¿ë±Ý±â ¹× ¿¬·É´ë±Ý±â ±Ù°ÅÁ¶È¸ |
[º´¿ë±Ý±â ¹× ¿¬·É´ë±Ý±â ±Ù°ÅÁ¶È¸]
|
| º¹¾à¶óº§ |
| À̹ÌÁö |
º¹¾à¼³¸í |
 |
º¯ºñ°¡ »ý±æ¼ö ÀÖ½À´Ï´Ù. |
|
 |
¾îÁö·¯¿òÀÌ ÀÖÀ»¼ö ÀÖ½À´Ï´Ù. |
|
|
| * |
º¹¾àÀ̹ÌÁö´Â ¸ðµç º¹¾àÁöµµ »çÇ×À» Ç¥½ÃÇѰÍÀº ¾Æ´Ï¸ç, Ãß°¡ÀûÀ¸·Î ¾÷µ¥ÀÌÆ®µÇ°Å³ª ¼öÁ¤µÉ ¼ö ÀÖ½À´Ï´Ù. |
| * |
º¹¾àÀ̹ÌÁöÀÇ Ç¥½Ã¿©ºÎ´Â ½ÇÁ¦ ¾à¹°º¹¿ë½Ã Á߿䵵¿¡ µû¸¥°ÍÀº ¾Æ´Ï¸ç ´Ü¼øÈ÷ Çã°¡Á¤º¸»ó Ű¿öµå¸¦ ±âÁØÀ¸·Î µî·ÏµÇ¾ú½À´Ï´Ù. |
| * |
±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. |
|
|
| º¸°ü»ó ÁÖÀÇ |
|
| Á¶Á¦½Ã ÁÖÀÇ |
|
|
|
 | ½É»çÁ¤º¸ |
|
|
|
|
 | ÇмúÁ¤º¸ |
|
|
| Ç׸ñ |
³»¿ë |
| 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]
¿¬·É´ë±Ý±â :
°í½ÃµÈ ¿¬·É±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
[¿¬·É´ë±Ý±â»ó¼¼°Ë»ö]
|
| Mechanism of Action |
Methyldopa¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Although the mechanism of action has yet to be conclusively demonstrated, the antihypertensive effect of methyldopa probably is due to its metabolism to alpha-methylnorepinephrine, which then lowers arterial pressure by stimulation of central inhibitory alpha-adrenergic receptors, false neurotransmission, and/or reduction of plasma renin activity. Methyldopa has been shown to cause a net reduction in the tissue concentration of serotonin, dopamine, norepinephrine, and epinephrine.
|
| Pharmacology |
Methyldopa¿¡ ´ëÇÑ Pharmacology Á¤º¸ Methyldopa is an aromatic-amino-acid decarboxylase inhibitor in animals and in man. Only methyldopa, the L-isomer of alpha-methyldopa, has the ability to inhibit dopa decarboxylase and to deplete animal tissues of norepinephrine. In man the antihypertensive activity appears to be due solely to the L-isomer. About twice the dose of the racemate (DL-alpha-methyldopa) is required for equal antihypertensive effect. Methyldopa has no direct effect on cardiac function and usually does not reduce glomerular filtration rate, renal blood flow, or filtration fraction. Cardiac output usually is maintained without cardiac acceleration. In some patients the heart rate is slowed. Normal or elevated plasma renin activity may decrease in the course of methyldopa therapy. Methyldopa reduces both supine and standing blood pressure. Methyldopa usually produces highly effective lowering of the supine pressure with infrequent symptomatic postural hypotension. Exercise hypotension and diurnal blood pressure variations rarely occur.
|
| Metabolism |
Methyldopa¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Catechol O-methyltransferase (COMT)
|
| Protein Binding |
Methyldopa¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Low (less than 20%).
|
| Half-life |
Methyldopa¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ The plasma half-life of methyldopa is 105 minutes.
|
| Absorption |
Methyldopa¿¡ ´ëÇÑ Absorption Á¤º¸ Absorption from the gastrointestinal tract is variable but averages approximately 50%.
|
| Pharmacokinetics |
MethyldopaÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- ÃÖ´ëÈ¿°ú ¹ßÇö½Ã°£ : °æ±¸, ÁÖ»ç : 3-6½Ã°£ À̳»
- ÀÛ¿ëÁö¼Ó½Ã°£ : 12-24½Ã°£
- ºÐÆ÷ : ÅÂ¹Ý Åë°ú, À¯Áó¿¡µµ ºÐÆ÷
- ´Ü¹é°áÇÕ : 15% ÀÌÇÏ
- ´ë»ç : ¼ÒÀå, °£¿¡¼ ´ë»ç
- ¹Ý°¨±â : 75-80ºÐ (¸»±â ½ÅºÎÀü : 6-16½Ã°£)
- ¹è¼³ : ´ëºÎºÐ(85%)ÀÌ 24½Ã°£ À̳»¿¡ ´ë»çü·Î ½Å ¹è¼³µÊ
|
| Biotransformation |
Methyldopa¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic, extensively metabolized. The known urinary metabolites are: a-methyldopa mono-0-sulfate; 3-0-methyl-a-methyldopa; 3,4-dihydroxyphenylacetone; a-methyldopamine; 3-0-methyl-a-methyldopamine and their conjugates.
|
| Toxicity |
Methyldopa¿¡ ´ëÇÑ Toxicity Á¤º¸ The oral LD50 of methyldopa is greater than 1.5 g/kg in both the mouse and the rat. Symptoms of overdose include bloating, constipation, diarrhea, dizziness, extreme drowsiness, gas, light-headedness, nausea, severely low blood pressure, slow heartbeat, vomiting, and weakness.
|
| Drug Interactions |
Methyldopa¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Carteolol Possible hypertensive crisisNadolol Possible hypertensive crisisOxprenolol Possible hypertensive crisisPenbutolol Possible hypertensive crisisPindolol Possible hypertensive crisisPropranolol Possible hypertensive crisisSotalol Possible hypertensive crisisTimolol Possible hypertensive crisisTerbutaline Increased arterial pressureSalbutamol Increased arterial pressurePseudoephedrine Increased arterial pressureProcaterol Increased arterial pressurePirbuterol Increased arterial pressurePhenylpropanolamine Increased arterial pressureOrciprenaline Increased arterial pressurePhenylephrine Increased arterial pressureNorepinephrine Increased arterial pressureMethoxamine Increased arterial pressureMetaraminol Increased arterial pressureMephentermine Increased arterial pressureIsoproterenol Increased arterial pressureIron Iron decreases the absorption of dopa derivativesLevodopa Methyldopa increases the effect and toxicity of levodopaLithium Signs of increased lithium levels without increase with this combinationDobutamine Increased arterial pressureDopamine Increased arterial pressureEphedra Increased arterial pressureEphedrine Increased arterial pressureEpinephrine Increased arterial pressureFenoterol Increased arterial pressureEntacapone Entacapone increases the effect and toxicity of sympathomimeticsHaloperidol Methyldopa increases haloperidol effect or risk of psychosis
|
CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
|
| Food Interaction |
Methyldopa¿¡ ´ëÇÑ Food Interaction Á¤º¸ Avoid alcohol.No iron, zinc or fluoride within 2 hours of taking this medication.May take Vitamin D.Avoid natural licorice.Increase dietary intake of magnesium, folate, vitamin B6, B12, and/or consider taking a multivitamin.Take without regard to meals.
|
| Drug Target |
[Drug Target]
|
| Description |
Methyldopa¿¡ ´ëÇÑ Description Á¤º¸ An alpha-2 adrenergic agonist that has both central and peripheral nervous system effects. Its primary clinical use is as an antihypertensive agent. [PubChem]
|
| Dosage Form |
Methyldopa¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Tablet Oral
|
| Drug Category |
Methyldopa¿¡ ´ëÇÑ Drug_Category Á¤º¸ Adrenergic alpha-AgonistsAntihypertensive AgentsSympatholytics
|
| Smiles String Canonical |
Methyldopa¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC(N)(CC1=CC(O)=C(O)C=C1)C(O)=O
|
| Smiles String Isomeric |
Methyldopa¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ C[C@](N)(CC1=CC(O)=C(O)C=C1)C(O)=O
|
| InChI Identifier |
Methyldopa¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C10H13NO4/c1-10(11,9(14)15)5-6-2-3-7(12)8(13)4-6/h2-4,12-13H,5,11H2,1H3,(H,14,15)/t10-/m0/s1/f/h14H
|
| Chemical IUPAC Name |
Methyldopa¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (2S)-2-amino-3-(3,4-dihydroxyphenyl)-2-methylpropanoic acid
|
|
|
 | »ç¿ëÀÚÄÁÅÙÃ÷ |
|
|
|
|
|
-
ÃÖ±ÙÁ¤º¸¼öÁ¤ÀÏ 2015-02-03
-
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.
|
|
¾Ë¸² |
»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. |
|
°æ°í |
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.
¹Ýµå½Ã Á¦Á¶¡¤¼öÀÔ»ç, ÆÇ¸Å»ç, ÀÇ»ç, ¾à»ç¿¡°Ô ÃÖÁ¾ÀûÀ¸·Î È®ÀÎÇϽñ⠹ٶø´Ï´Ù.
ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
|
|
¾Æ·¡ÀÇ ³»¿ëÀ» Æ÷ÇÔÇÑ Àüü µ¥ÀÌÅ͸¦ º¸½Ã·Á¸é
¿©±â·Î À̵¿ÇϽñ⠹ٶø´Ï´Ù.
The database contains the following fields: The generic name of each chemical For module A10 (liver enzyme composite module): Overall activity category for each compound (A for active, M for marginally active, or I for inactive) based on the number of active and marginally active scores for each compound at the five individual endpoints (see research article for full description of method) Number of endpoints at which each compound is marginally active (M) Number of endpoints at which each compound is active (A) For modules A11 to A15 (alkaline phosphatase increased, SGOT increased, SGPT increased, LDH increased, and GGT increased, respectively): Overall activity category for each compound (A for active, M for marginally active, or I for inactive) based on the RI and ADR values (see the research article for full description of method) Number of ADR reports for each compound, given as <4 or ¡Ã4 Reporting Index value for each compound, except where no shipping units were available (NSU) Group 1 comprises of compounds for which ADR data were available for the first five years of marketing, so when no ADR reports were listed during this period the compounds were evaluated as inactive. Group 2 comprises of compounds for which a 'steady state' period of ADR data were available (1992-1996). In cases where no ADR reports were filed during this period, the compounds were scored as 'NA' (data not available) since they may have had one or more ADR reports during their first five years of marketing which should not be negated by a lack of ADR reports during the steady-state period. METHYLDOPA[GGT Increase][Composite Activity](Score) NA(Marginal) 0(Active) 0[Alkaline Phosphatase Increase](Activity Score) NA(Number of Rpts) NA(Index value) NA[SGOT Increase](Activity Score) NA(Number of Rpts) NA(Index value) NA[SGPT Increase](Activity Score) NA(Number of Rpts) NA(Index value) NA[LDH Increase](Activity Score) NA(Number of Rpts) NA(Index value) NA[GGT Increase](Activity Score) NA(Number of Rpts) NA(Index value) NA
º´¿ë±Ý±â ¹× ƯÁ¤¿¬·É´ë ±Ý±â ¼ººÐ
[ÀǾàǰº´¿ë/¿¬·É´ë±Ý±â °í½Ã±Ù°Å·Î ¹Ù·Î°¡±â] Á¦¸ñ ¾øÀ½
2008³â 8¿ù 1ÀÏ ¾à°¡ÈÀÏ»ó 8¿ù´Þ ½Å±ÔµîÀç ¹× »èÁ¦µÇ´Â ǰ¸ñ Æ÷ÇÔÇÑ º´¿ë¿¬·É ±Ý±â ǰ¸ñ¸®½ºÆ® ±âÁØ
1. ÇöÀç °Ë»öÇÑ Á¦Ç°¿¡ ´ëÇÑ º´¿ë±Ý±â Á¦Ç° Á¸Àç¿©ºÎ ¹× °Ë»ö
ÇöÀç ÀÌÁ¦Ç°¿¡ ´ëÇÑ º´¿ë±Ý±â¿¡ ÇØ´çÇϴ û±¸Äڵ庰 Á¦Ç°³»¿ª °øÁö³»¿ëÀÌ ¾ø½À´Ï´Ù
2. ¿¬·É´ë±Ý±â Á¸Àç¿©ºÎ
ÇöÀç ÀÌÁ¦Ç°¿¡ ´ëÇÑ ¿¬·É±Ý±â¿¡ ÇØ´çÇϴ û±¸Äڵ庰 °øÁö³»¿ëÀÌ ¾ø½À´Ï´Ù
|