| |
|
|
|
|
|
 |
| |
|
¿øÆ¿¶ó°Ö WONTILLA GEL
|
|
Àü¹®ÀǾàǰ | ºñ±Þ¿©
|
|
|
| |
 |
¾Ë¸²: |
µå·°ÀÎÆ÷¿¡¼´Â ÀǾàǰ ÀÎÅÍ³Ý ÆÇ¸Å¸¦ ÇÏÁö ¾Ê½À´Ï´Ù. |
|
|
|
|
|
|
|
 |
|
|
|
|
|
|
 |
Á¦Ç°º° ¿¬·É±Ý±â °í½Ã |
|
|
| ¼ººÐ¸í |
¼ººÐÄÚµå |
ƯÁ¤¿¬·É |
°í½Ã¹øÈ£ |
°í½ÃÀÏÀÚ |
ºñ°í |
| chlorhexidine gluconate solution, lidocaine hydrochloride |
660100CCM |
24 °³¿ù ¹Ì¸¸ |
20180088 |
2018-11-02 |
|
|
|
|
|
|
|
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× |
645906051
[º¸ÇèÄڵ忡 µû¸¥ ¾àǰ±âº»Á¤º¸ Á÷Á¢Á¶È¸]
[ºñ±Þ¿©]
[»óº´ÄÚµåÁ¶È¸]
[Áúº´ÄÚµåÁ¶È¸]
|
| ºü¸¥Á¶È¸ |
|
| Á¦Ç°¼º»ó |
¹«»öÅõ¸íÇÑ ÇÁ¸®Çʵå½Ã¸°Áö¿¡ ¹«»ö ³»Áö °ÅÀÇ ¹«»öÀÇ Åõ¸íÇÑ °ÖÁ¦ [Á¦ÇüÁ¤º¸ È®ÀÎ] |
| Æ÷À塤À¯Åë´ÜÀ§ |
10°ü/»óÀÚ(6¹Ð¸®¸®ÅÍ/°ü) |
| ÁÖ¼ººÐÄÚµå |
660100CCM
[µ¿ÀÏÇÑ ÁÖ¼ººÐÄڵ带 °¡Áø ¿À¸®Áö³¯ ¶Ç´Â Á¦³×¸¯ ÀǾàǰ Á¶È¸]
|
| Çã°¡»çÇ× ¿ø¹®Á¶È¸ |
[Çã°¡»çÇ× ¿ø¹®Á¶È¸]
|
| È¿´ÉÈ¿°ú |
[ÀûÀÀÁõ º° °Ë»ö]
´ÙÀ½ ½Ã¼ú½Ã Ç¥¸é¸¶Ãë, ¼Òµ¶, À±È°ÀÛ¿ë :
Ä«Å×ÅÍ »ðÀÔ, ¿äµµ(³²¼º¡¤¿©¼º)³» ¼ö¼ú, °¢Á¾ ³»½Ã°æ °Ë»ç, »ð°ü, ½Ã¼ú·Î ÀÎÇÑ Á÷Àå°ú °áÀå¿¡¼ÀÇ ¼Õ»ó ¿¹¹æ
|
| ¿ë¹ý¿ë·® |
* Àý´ë ÀÓÀǺ¹¿ëÇÏÁö ¸¶½Ã°í ¹Ýµå½Ã ÀÇ»ç ¶Ç´Â ¾à»ç¿Í »ó´ãÇϽñ⠹ٶø´Ï´Ù.
[󹿾à¾î]
1. Ä«Å×ÅÍ»ðÀÔ
ÀÌ ¾à 6 mL ¶Ç´Â 11 mL¸¦ ÁÖÀÔÇÑ´Ù. ±ÍµÎ¿Í ¿äµµ¸¦ ±ú²ýÀÌ ÇÑ ÈÄ ¿äµµ¿¡ ¼¼È÷ ÁÖÀÔÇÏ°í ±¹¼Ò¸¶Ãë¿Í ¼Òµ¶È¿°ú°¡ ³ªÅ¸³¾ ¶§±îÁö ±ÍµÎ¸¦ ¾Ð¹ÚÇÑ´Ù.
2. ¹æ±¤°æ°Ë»ç
ÀÌ ¾à 11 mL¸¦ »ç¿ëÇϸç, ÇÊ¿ä½Ã 6 mL ¶Ç´Â 11 mL¸¦ Ãß°¡·Î ÁÖÀÔÇÑ´Ù. ¿ÜºÎÁ¶ÀÓ±ÙÀ» Æ÷ÇÔÇÏ¿© Àüü¿äµµ¿¡ µµÆ÷ÇÑ´Ù.
3. ¿äµµÇùÂø(¿äµµ±¸Àý°³¼ú)
ÀÌ ¾à 11 mL¸¦ »ç¿ëÇϸç, ÇÊ¿ä½Ã 6 mL ¶Ç´Â 11 mL¸¦ Ãß°¡·Î ÁÖÀÔÇϰí Ŭ·¥ÇÁ·Î Áý¾îÁØ´Ù. ¿äµµ ¸¶ÃëÈ¿°ú´Â 5 ¡ 10ºÐ ÈÄ ³ªÅ¸³´Ù.
4. ¼Òµ¶
ÀÌ ¾à 6 mL ¶Ç´Â 11 mL ¸¦ Á¡¸·¿¡ °ñ°í·ç ¹Ù¸£°Å³ª ÁÖÀÔÇÑ´Ù.
5. ±âŸ
Àû¿ëºÎÀ§¿¡ 6 mL ¶Ç´Â 11 mL¸¦ õõÈ÷ ÁÖÀÔÇϸç, »ðÀÔµÉ Ä«Å×Åͳª ½Ã¼úµµ±¸¿¡ °ñ°í·ç µµÆ÷ÇÑ´Ù.
±¹¼Ò¸¶Ãë ¹× ¼Òµ¶È¿°ú´Â 5 ¡ 10ºÐ ÈÄ¿¡ ³ªÅ¸³´Ù.
|
| ±Ý±â |
1) ¾Æ¹Ìµå°è ¸¶ÃëÁ¦, Ŭ·Î¸£Çí½ÃµòÁ¦Á¦ ¶Ç´Â ¾ËųÆÄ¶ó¿Á½Ãº¥Á¶»ê µî ÀÌ ¾àÀÇ ¼ººÐ¿¡ ´ëÇÏ¿© °ú¹Î¹ÝÀÀÀÌ Àִ ȯÀÚ
2) ¼Õ»óµÈ ÇǺÎ, ´« ¹× ´«ÁÖÀ§
3) ³ú, ô¼ö, ±Í(³»ÀÌ, ÁßÀÌ, ¿ÜÀÌ)(û°¢½Å°æ ¶Ç´Â ÁßÃ߽Ű濡 Á÷Á¢ »ç¿ëÇÒ °æ¿ì ³Ã», ½Å°æÀå¾Ö¸¦ ÀÏÀ¸Å³ ¼ö ÀÖ´Ù)
4) Æ÷¸£ÇǸ°Áõ
5) Á¶ÀýµÇÁö ¾Ê´Â °£Áú
6) ÁßÁõÀÇ ½ÉÀåÀüµµ ÀÌ»ó
7) 2¼¼ ¹Ì¸¸ÀÇ ¼Ò¾Æ |
| ½ÅÁßÅõ¿© |
1) Àû¿ë ºÎÀ§¿¡ Á¡¸·ÀÇ ¿Ü»óÀÌ Àִ ȯÀÚ ¶Ç´Â ÆÐÇ÷Áõ ȯÀÚ
2) °£Áú ȯÀÚ
3) ½ÉÀå Àüµµ ÀÌ»ó, ¼¸Æ, °£±â´É ¼Õ»ó, ÁßÁõÀÇ ¼îÅ© ȯÀÚ
4) õ½Ä µî ¾Ë·¹¸£±â Áúȯ ¹× ±× º´·Â ¶Ç´Â °¡Á··ÂÀÌ Àִ ȯÀÚ
5) ÀӺΠ¹× ÀÓ½ÅÇϰí ÀÖÀ» °¡´É¼ºÀÌ ÀÖ´Â ¿©¼º ¶Ç´Â ¼öÀ¯ºÎ
|
| ÀÌ»ó¹ÝÀÀ |
1) ¼îÅ© : ¼îÅ©°¡ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÃæºÐÈ÷ °üÂûÇϰí Ç÷¾ÐÀúÇÏ, ¾È¸éâ¹é, ¸Æ¹ÚÀÇ ÀÌ»ó, È£Èí¾ïÁ¦, ±¸¿ª, ºÒÄè°¨, ½ÄÀº¶¡, ¾îÁö·³, ´ä´äÇÔ, ¹ßÀû µîÀÌ ³ªÅ¸³ª´Â °æ¿ì¿¡´Â Áï½Ã »ç¿ëÀ» ÁßÁöÇϰí ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù.
2) ½Å°æ°è
(1) ÁøÀü, °æ·Ã µîÀÇ ÁßÁõÀÇ ½É°¢ÇÑ Áõ»óÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÃæºÐÈ÷ °üÂûÇϰí ÀÌ·¯ÇÑ Áõ»óÀÌ ³ªÅ¸³ª´Â °æ¿ì¿¡´Â Áï½Ã Åõ¿©ÁßÁöÇÏ°í µð¾ÆÁ¦ÆÊ ¶Ç´Â Ãʴܽð£Çü ¹Ù¸£ºñÅ»»ê Á¦Á¦(Ƽ¿ÀÆæÅ»³ªÆ®·ý) Åõ¿© µî ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù.
(2) Á¹À½, ºÒ¾È, ÈïºÐ, ¹«½Ã, ¾îÁö·³, ±¸¿ª¡¤±¸Åä, ½Å°æ°ú¹Î, ÀǽļҽÇ, ºÒÄè°¨, ½ÄÀº¶¡, ´ä´äÇÔ, ÇÇ·Î, ¹æÇâ°¨°¢»ó½Ç, ¾ÈÀå¾Ö, ¾ð¾îÀå¾Ö, ±Í¿ï¸², °æ·Ã, °¨°¢ÀÌ»ó(ÀÚÁÖ Åõ¿©½Ã), ÀÌ»óȲȦ°¨, ȯ°¢, ¿ì¿ï, È¥¼ö, ÀϹݰæ·Ã, È£ÈíÀúÇÏ(µå¹°°Ô, ƯÈ÷ °ú·®Åõ¿©½Ã), ÃÊÁ¶, ÇÏǰ, ¶³¸², °ÆÁ¤, ´«¶³¸², º´Àû´Ùº¯Áõ, µÎÅë, ±Í¿ï¸², ¹ÝÀÀ´À¸², ÈïºÐ µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÃæºÐÈ÷ °üÂûÇÏ¿© ¼îÅ© ¶Ç´Â ÁßÁõÀÇ ½É°¢ÇÑ Áõ»óÀ¸·Î ÀÌÇàÇÏ´Â °Í¿¡ ÁÖÀÇÇϰí Çʿ信 µû¶ó ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù.
3) ½ÉÇ÷°ü°è
ÀúÇ÷¾Ð, ½É±Ù¾ïÁ¦, ¼¸Æ, ½ÉÁ¤Áö, ºÎÁ¤¸Æ, ¹æ½Çºí·Ï, ½É½Ç¼¼µ¿(°æ¿ì¿¡ µû¶ó), ºó¸Æ, °íÇ÷¾Ð, ±â´ÉÀúÇÏÁö¼Ó µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
4) È£Èí±â°è
ºü¸¥È£Èí ¹× È£Èí°ï¶õ
5) À§Àå°ü°è
±¸¿ª¡¤±¸Åä¿Í °°Àº À§Àå°ü ºÒÄè°¨(ÀÚÁÖ Åõ¿© ½Ã)
6) °ú¹Î¹ÝÀÀ : ¶§¶§·Î ¹ßÀû, ¹ßÁø, µÎµå·¯±â µîÀÇ ÇǺÎÁõ»ó ¹× ºÎÁ¾ÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¸ç ÀÌ·¯ÇÑ °æ¿ì¿¡´Â Áï½Ã »ç¿ëÀ» ÁßÁöÇÑ´Ù.
7) °ú·®Åõ¿©½Ã ¿äµµ¼Õ»óÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
8) µå¹°°Ô Ŭ·Î¸£Çí½Ãµò¿¡ ÀÇÇÑ Á¢Ã˺ÎÀ§ÀÇ ¾Ë·¹¸£±â ½ÀÁøÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
9) ±¤¼±¹Î°¨È°¡ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
|
| »óÈ£ÀÛ¿ë |
1) ÀÌ ¾à°ú ºÎÁ¤¸Æ¿ëÁ¦(ÅäÄ«ÀÌ´Ïµå µî)¸¦ º´¿ëÅõ¿©ÇÏ´Â °æ¿ì, ÀÌ»ó¹ÝÀÀÀÌ Áõ°µÉ ¼ö ÀÖÀ¸¹Ç·Î ÁÖÀÇÇÑ´Ù.
2) µ¿¹°½ÇÇè°á°ú ÀÌ ¾à°ú ÆäƼµòÀ» º´¿ëÅõ¿©½Ã ¸®µµÄ«ÀÎÀÇ µ¶¼ºÀÌ Áõ°¡µÉ ¼ö ÀÖÀ¸¹Ç·Î ÁÖÀÇÇÑ´Ù.
3) Ŭ·Î¸£Çí½ÃµòÀº ¾çÀ̿¼º »ì±ÕÁ¦À̹ǷΠÀ½À̿¼º ¹°Áú(ºñ´©)°ú ÇÔ²² »ç¿ëÇÏÁö ¾Ê´Â´Ù. |
| Off-label Usage |
[Á¶È¸]
|
| 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.
|
| Ãà¾àº¹¾àÁöµµ |
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
(lidocaine; )
|
|
| * |
»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.
|
|
|
| º¹¾à¶óº§ |
| À̹ÌÁö |
º¹¾à¼³¸í |
 |
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]
|
| µ¶¼ºÁ¤º¸ |
Lidocaine¿¡ ´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 |
Chlorhexidine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Chlorhexidine's antimicrobial effects are associated with the attractions between chlorhexidine (cation) and negatively charged bacterial cells. After chlorhexidine is absorpted onto the organism's cell wall, it disrupts the integrity of the cell membrane and causes the leakage of intracellular components of the organisms.
Lidocaine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Lidocaine stabilizes the neuronal membrane by inhibiting the ionic fluxes required for the initiation and conduction of impulses thereby effecting local anesthetic action.
|
| Pharmacology |
Chlorhexidine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Chlorhexidine, a topical antimicrobial agent, is bactericidal. Because of its positive charge, the chlorhexidine molecule reacts with the microbial cell surface to destroy the integrity of the cell membrane. This novel mechanism of action makes it highly unlikely for the development of bacterial resistance.
Lidocaine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Lidocaine is an anesthetic agent indicated for production of local or regional anesthesia and in the treatment of ventricular tachycardia occurring during cardiac manipulation, such as surgery or catheterization, or which may occur during acute myocardial infarction, digitalis toxicity, or other cardiac diseases. The mode of action of the antiarrhythmic effect of Lidocaine appears to be similar to that of procaine, procainamide and quinidine. Ventricular excitability is depressed and the stimulation threshold of the ventricle is increased during diastole. The sinoatrial node is, however, unaffected. In contrast to the latter 3 drugs, Lidocaine in therapeutic doses does not produce a significant decrease in arterial pressure or in cardiac contractile force. In larger doses, lidocaine may produce circulatory depression, but the magnitude of the change is less than that found with comparable doses of procainamide.
|
| Metabolism |
Chlorhexidine¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Not Available
Lidocaine¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 1A2 (CYP1A2)Cytochrome P450 2D6 (CYP2D6)
|
| Absorption |
Chlorhexidine¿¡ ´ëÇÑ Absorption Á¤º¸ Absorption of chlorhexidine from the gastrointestinal tract is very poor. Additionally, an in vivo study in 18 adult patients found no detectable plasma or urine chlorhexidine concentrations following insertion of four periodontal implants under clinical conditions.
Lidocaine¿¡ ´ëÇÑ Absorption Á¤º¸ Information derived from diverse formulations, concentrations and usages reveals that lidocaine is completely absorbed following parenteral administration, its rate of absorption depending, for example, upon various factors such as the site of administration and the presence or absence of a vasoconstrictor agent.
|
| Toxicity |
Chlorhexidine¿¡ ´ëÇÑ Toxicity Á¤º¸ LD50= 2g/kg (human, oral); LD50= 3 g/kg (rat, oral); LD50= 2.5 g/kg (mice, oral); LD50= 21 mg/kg (male rat, IV); LD50= 23 mg/kg (female rat, IV); LD50= 25 mg/kg (male mice, IV); LD50= 24 mg/kg (female mice, IV); LD50= 1g/kg (rat, subcutaneous); LD50= 637 mg/kg (male mice, subcutaneous); LD50= 632 mg/kg (female mice, subcutaneous)
Lidocaine¿¡ ´ëÇÑ Toxicity Á¤º¸ The oral LD 50 of lidocaine HCl in non-fasted female rats is 459 (346-773) mg/kg (as the salt) and 214 (159-324) mg/kg (as the salt) in fasted female rats. Symptoms of overdose include convulsions, hypoxia, acidosis, bradycardia, arrhythmias and cardiac arrest.
|
| Drug Interactions |
Chlorhexidine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
Lidocaine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
|
CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
|
| Food Interaction |
Lidocaine¿¡ ´ëÇÑ Food Interaction Á¤º¸ Not Available
|
| Drug Target |
[Drug Target]
|
| Description |
Chlorhexidine¿¡ ´ëÇÑ Description Á¤º¸ A disinfectant and topical anti-infective agent used also as mouthwash to prevent oral plaque. [PubChem]
Lidocaine¿¡ ´ëÇÑ Description Á¤º¸ A local anesthetic and cardiac depressant used as an antiarrhythmia agent. Its actions are more intense and its effects more prolonged than those of procaine but its duration of action is shorter than that of bupivacaine or prilocaine. [PubChem]
|
| Dosage Form |
Chlorhexidine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Aerosol TopicalDressing TopicalGel TopicalKit DentalLiquid BuccalLiquid OralLiquid TopicalLotion TopicalOintment TopicalSolution TopicalSponge Topical
Lidocaine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Aerosol TopicalAerosol, metered TopicalCream TopicalGel TopicalJelly TopicalJelly UrethralLiquid BuccalLiquid DentalLiquid InfiltrationLiquid IntravenousLiquid OralLiquid TopicalLotion TopicalOintment TopicalSolution InfiltrationSolution IntramuscularSolution IntravenousSolution OralSolution TopicalSpray TopicalSwab Topical
|
| Drug Category |
Chlorhexidine¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Bacterial AgentsAnti-Infective Agents, LocalAnti-InfectivesDisinfectantsMouthwashes
Lidocaine¿¡ ´ëÇÑ Drug_Category Á¤º¸ AnestheticsAnesthetics, LocalAnti-Arrhythmia AgentsAntiarrhythmic Agents
|
| Smiles String Canonical |
Chlorhexidine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ NC(NC1=CC=C(Cl)C=C1)=NC(N)=NCCCCCCN=C(N)N=C(N)NC1=CC=C(Cl)C=C1
Lidocaine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CCN(CC)CC(=O)NC1=C(C)C=CC=C1C
|
| Smiles String Isomeric |
Chlorhexidine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ N\C(NC1=CC=C(Cl)C=C1)=N/C(N)=N/CCCCCC\N=C(N)\N=C(/N)NC1=CC=C(Cl)C=C1
Lidocaine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CCN(CC)CC(=O)NC1=C(C)C=CC=C1C
|
| InChI Identifier |
Chlorhexidine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C22H30Cl2N10/c23-15-5-9-17(10-6-15)31-21(27)33-19(25)29-13-3-1-2-4-14-30-20(26)34-22(28)32-18-11-7-16(24)8-12-18/h5-12H,1-4,13-14H2,(H5,25,27,29,31,33)(H5,26,28,30,32,34)/f/h31-32H,25-28H2/b29-19+,30-20+,33-21+,34-22+
Lidocaine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C14H22N2O/c1-5-16(6-2)10-13(17)15-14-11(3)8-7-9-12(14)4/h7-9H,5-6,10H2,1-4H3,(H,15,17)/f/h15H
|
| Chemical IUPAC Name |
Chlorhexidine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (1E)-2-[6-[[amino-[[amino-[(4-chlorophenyl)amino]methylidene]amino]methylidene]amino]hexyl]-1-[amino-[(4-chlorophenyl)amino]methylidene]guanidine
Lidocaine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 2-diethylamino-N-(2,6-dimethylphenyl)acetamide
|
| Drug-Induced Toxicity Related Proteins |
DOCA ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸ Replated Protein:Aquaporin-2 Drug:DOCA Toxicity:hypertension. [¹Ù·Î°¡±â] LIDOCAINE ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸ Replated Protein:glucose-regulated protein Drug:lidocaine Toxicity:intestinal disorder. [¹Ù·Î°¡±â] Replated Protein:Alkaline phosphatase Drug:lidocaine Toxicity:lidocaine induced hepatitis. [¹Ù·Î°¡±â] Replated Protein:C-reactive protein Drug:lidocaine Toxicity:fever. [¹Ù·Î°¡±â] Replated Protein:C-reactive protein Drug:lidocaine Toxicity:lidocaine induced hepatitis. [¹Ù·Î°¡±â] Replated Protein:Alpha-1-acid glycoprotein Drug:lidocaine Toxicity:lidocaine tolerance. [¹Ù·Î°¡±â] Replated Protein:Gamma-glutamyltranspeptidase Drug:lidocaine Toxicity:fever. [¹Ù·Î°¡±â] Replated Protein:Alkaline phosphatase Drug:lidocaine Toxicity:fever. [¹Ù·Î°¡±â] Replated Protein:Gamma-glutamyltranspeptidase Drug:lidocaine Toxicity:lidocaine induced hepatitis. [¹Ù·Î°¡±â]
|
|
|
 | »ç¿ëÀÚÄÁÅÙÃ÷ |
|
|
|
|
|
-
ÃÖ±ÙÁ¤º¸¼öÁ¤ÀÏ 2022-12-26
-
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.
º´¿ë±Ý±â ¹× ƯÁ¤¿¬·É´ë ±Ý±â ¼ººÐ
|
|
|
|