³ëÆæÇÏÀÌīŸÇö󽺸¶(Ç÷縣ºñÇÁ·ÎÆæ)
ÀϹÝÀǾàǰ | ºñ±Þ¿©
¾Ë¸²:
µå·°ÀÎÆ÷¿¡¼´Â ÀǾàǰ ÀÎÅÍ³Ý ÆÇ¸Å¸¦ ÇÏÁö ¾Ê½À´Ï´Ù.
Àü¹®/ÀϹÝ
ÀϹÝ
¿¬Çѳë¶õ»ö ¶Ç´Â ¹«»öÀÇ ¾à¾×À» °íüÇǺ¹¹°»ó¿¡ µµÆ÷ÇÏ°í ºÎÁ÷Æ÷¸¦ µ¤Àº īŸÇö󽺸¶Á¦
Á¦Á¶È¸»ç
Á¦ÀÌ´õºíÀ¯Áß¿ÜÁ¦¾à(ÁÖ)
ÆÇ¸Åȸ»ç
Á¦ÀÌ´õºíÀ¯Áß¿ÜÁ¦¾à(ÁÖ)
Çã°¡Á¤º¸
ÃëÇÏ
(2022.06.09)
BIT ¾àÈ¿ºÐ·ù
¿Ü¿ë ¼Ò¿°ÁøÅëÁ¦ (NSAIDs : Skin & Mucous Membrane)
º¹ÁöºÎºÐ·ù
264[ÁøÅ롤Áø¾ç¡¤¼ö·Å¡¤¼Ò¿°Á¦ ]
û±¸ÄÚµå(KDÄÚµå) ºñ±Þ¿©Á¡°ËÄÚµå
644914380 [ºñ±Þ¿©]
ATCÄÚµå
Flurbiprofen / M02AA19
NDCÄÚµå
[Proprietary Name Search _ ƯÇãµî·Ï¸í,»óÇ¥¸íÀ¸·Î °Ë»ö]
[Active Ingredient Search _ ÁÖ¼ººÐÀ¸·Î °Ë»ö]
[NDC Number Search _ NDCÄÚµå·Î °Ë»ö]
¼ººÐ / ÇÔ·®
[½ÉÆò¿ø ÁÖ¼ººÐÄÚµå ±âÁØ ¼ººÐÇÔ·®Á¤º¸ Á¶È¸]
÷°¡Á¦
±Û¶óÀÌÄÝ Ç츶-¸ÞŸũ¸±·¹ÀÌÆ® ,
³ó±Û¸®¼¼¸° ,
¶ó¿ì¸±ÇǷѸ®µ· ,
¹Ù´ÒºÎÆ¿¿¡Å׸£ ,
º¥Á¶Æä³í ,
ºÎÁ÷Æ÷ ,
¼Ò¸£ºñź¿Ã·¹¿¡ÀÌÆ® ,
½Ç¸®ÄÚ³ªÀÌÁîµåÆú¸®¿¡½ºÅ׸£Çʸ§ ,
Á¤Á¦¼ö ,
Ÿ¸£Å¸¸£»ê ,
ÆÄ¶ó¿Á½Ãº¥Á¶»ê¸ÞÆ¿ ,
ÆÄ¶ó¿Á½Ãº¥Á¶»êÇÁ·ÎÇÊ ,
Æ÷ºñµ· ,
Æú¸®¼Ò¸£º£ÀÌÆ®80 ,
Æú¸®¾ÆÅ©¸±»ê¾× ,
ÇÁ·ÎÇÊ·»±Û¸®ÄÝ ,
D-¼Ò¸£ºñÅç¿ë¾× ,
L-¸àÅç
À¯·áȸ¿ø °áÀç½Ã ¿¡´Â º¸´Ù ´Ù¾çÇÑ ¾à¹°Á¤º¸ ¸¦
ÀÌ¿ë ÇÏ½Ç ¼ö ÀÖ½À´Ï´Ù.
À¯·áÁ¤º¸¸ñ·Ï Àº Àü¹®È¸¿ø À¸·Î
·Î±×ÀÎ ÇϽøé È®ÀÎ °¡´ÉÇÕ´Ï´Ù.
Çã°¡Á¤º¸
Ç׸ñ
³»¿ë
û±¸ÄÚµå(KDÄÚµå) ºñ±Þ¿©Á¡°ËÄÚµå »óÇѱݾ×
644914380
[º¸ÇèÄڵ忡 µû¸¥ ¾àǰ±âº»Á¤º¸ Á÷Á¢Á¶È¸]
[ºñ±Þ¿©]
[»óº´ÄÚµåÁ¶È¸]
[Áúº´ÄÚµåÁý ´Ù¿î·Îµå]
[¿ì¸®Áý°Ç°ÁÖÄ¡ÀÇ ¹Ù·Î°¡±â]
ºü¸¥Á¶È¸
Á¦Ç°¼º»ó
¿¬Çѳë¶õ»ö ¶Ç´Â ¹«»öÀÇ ¾à¾×À» °íüÇǺ¹¹°»ó¿¡ µµÆ÷ÇÏ°í ºÎÁ÷Æ÷¸¦ µ¤Àº īŸÇö󽺸¶Á¦
[Á¦ÇüÁ¤º¸ È®ÀÎ]
Æ÷À塤À¯Åë´ÜÀ§
5¸Å/Æ÷, 6¸Å/Æ÷, 7¸Å/Æ÷
Æ÷À塤ÄÚµå´ÜÀ§
¾àǰ±Ô°Ý
´ÜÀ§
´ëÇ¥ÄÚµå
Ç¥ÁØÄÚµå
ºñ°í
20¹Ð¸®±×·¥
7 ¸Å
8806449143801
8806449143818
1¸Å(7.09cmX10cm)
ÁÖ¼ººÐÄÚµå
161904CPO
[µ¿ÀÏÇÑ ÁÖ¼ººÐÄڵ带 °¡Áø ¿À¸®Áö³¯ ¶Ç´Â Á¦³×¸¯ ÀǾàǰ Á¶È¸]
´ëÇ¥ÄÚµå
8806449143801
º¸°ü¹æ¹ý
±â¹Ð¿ë±â, ½Ç¿Â(1¢¦30¡É)º¸°ü
¾à¸®ÀÛ¿ë
[Á¶È¸]
È¿´ÉÈ¿°ú
[ÀûÀÀÁõ º° °Ë»ö]
´ÙÀ½ Áúȯ ¹× Áõ»óÀÇ ÁøÅë, ¼Ò¿°(Ç׿°)
- ÅðÇ༺°üÀý¿°(°ñ(»À)°üÀý¿°), ¾î±ú°üÀýÁÖÀ§¿°, °Ç․ °ÇÃÊ¿°(ÈûÁÙÀ±È°¸·¿°), »ó¿Ï°ñ(À§ÆÈ»À)»ó°ú¿° (Å״Ͻº¿¤º¸¿ì µî), ±ÙÀ°Åë, ¿Ü»ó(»óó)ÈÄÀÇ Á¾Ã¢(ºÎ±â)․ µ¿Åë(ÅëÁõ)
¿ë¹ý¿ë·®
* Àý´ë ÀÓÀǺ¹¿ëÇÏÁö ¸¶½Ã°í ¹Ýµå½Ã ÀÇ»ç ¶Ç´Â ¾à»ç¿Í »ó´ãÇϽñ⠹ٶø´Ï´Ù.
[󹿾à¾î]
¾à¸éÀÇ ¹Ú¸®Áö¸¦ ¶¼¾î³½ ÈÄ 1ÀÏ 2ȸ ȯºÎ¿¡ ºÎÂøÇÑ´Ù.
±Ý±â
1) ÀÌ ¾à ¹× ±âŸÀÇ Ç÷縣ºñÇÁ·ÎÆæ Á¦Á¦¿¡ °ú¹ÎÁõÀÇ º´·ÂÀÌ Àִ ȯÀÚ
2) ¾Æ½ºÇǸ° õ½Ä(ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°(Ç׿°)ÁøÅëÁ¦ µî¿¡ ÀÇÇÑ Ãµ½Ä¹ßÀÛÀÇ À¯¹ß) ¶Ç´Â ±× º´·ÂÀÌ Àִ ȯÀÚ(õ½Ä¹ßÀÛÀ» À¯¹ßÇÏ´Â °æ¿ì°¡ ÀÖ´Ù)
½ÅÁßÅõ¿©
±â°üÁö õ½Ä ȯÀÚ(õ½Ä¹ßÀÛÀ» ÀÏÀ¸Å³ ¼ö ÀÖ´Ù)
ÀÌ»ó¹ÝÀÀ
1) ¶§¶§·Î ¹ßÀû(ÃæÇ÷µÇ¾î ºÓ¾îÁü), ¹ßÁø, ¾àÁø(¾à¹°¹ßÁø), °¡·Á¿ò ¹× ÀÛ¿°¨(Ȳö°¨), Á¢ÃËÇǺο°ÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¸ç ÀÌ·¯ÇÑ Áõ»óÀÌ ³ªÅ¸³¯ °æ¿ì¿¡´Â »ç¿ëÀ» ÁßÁöÇÑ´Ù.
2) õ½Ä¹ßÀÛÀ» À¯¹ßÇÒ ¼ö ÀÖÀ¸¹Ç·Î °Ç¼º¼öÆ÷À½, õ¸í(¼ûÀ» ½Ù½Ù°Å¸²), È£Èí°ï¶õ µîÀÇ ÃʱâÁõ»óÀÌ ³ªÅ¸³¯ °æ¿ì¿¡´Â »ç¿ëÀ» ÁßÁöÇÑ´Ù. õ½Ä¹ßÀÛÀº ÀÌ ¾àÀÇ ºÎÂø ÈÄ ¼ö ½Ã°£ ³»¿¡ ³ªÅ¸³´Ù.
ÀϹÝÀû ÁÖÀÇ
1) ¼Ò¿°(Ç׿°)ÁøÅëÁ¦¿¡ ÀÇÇÑ Ä¡·á´Â ¿øÀοä¹ýÀÌ ¾Æ´Ñ ´ëÁõ¿ä¹ý(Áõ»óº°·Î Ä¡·áÇÏ´Â ¹æ¹ý)ÀÓ¿¡ À¯ÀÇÇÑ´Ù.
2) ÇǺΰ¨¿°ÁõÀ» ºÒÇö¼º(Áõ»óÀÌ ³ªÅ¸³ªÁö ¾Ê´Â)È ½Ãų ¼ö ÀÖÀ¸¹Ç·Î °¨¿°À» ¼ö¹ÝÇÏ´Â ¿°Áõ¿¡ »ç¿ëÇÏ´Â °æ¿ì¿¡´Â ÀûÀýÇÑ Ç×±ÕÁ¦ ¶Ç´Â Ç×Áø±Õ(Ç×°õÆÎÀÌ)Á¦¸¦ º´¿ë(ÇÔ²² º¹¿ë)Çϰí ÃæºÐÈ÷ °üÂûÇÏ¿© ½ÅÁßÈ÷ Åõ¿©ÇÑ´Ù.
3) ¸¸¼ºÁúȯ(ÅðÇ༺°üÀý¿°(°ñ(»À)°üÀý¿°) µî)¿¡ ÀÌ ¾àÀ» »ç¿ëÇÒ °æ¿ì¿¡´Â ¾à¹°¿ä¹ý ÀÌ¿ÜÀÇ ¿ä¹ýµµ °í·ÁÇÑ´Ù. ¶ÇÇÑ È¯ÀÚÀÇ »óŸ¦ ÃæºÐÈ÷ °üÂûÇÏ¿© ºÎÀÛ¿ë ¹ßÇö(µå·¯³¿)¿¡ À¯ÀÇÇÑ´Ù.
ÀӺο¡ ´ëÇÑ Åõ¿©
[ÀӺαݱ⠼ººÐ Á¶È¸]
ÀӽŠÁ¦ 1,2 »ïºÐ±â¿¡´Â ¸í¹éÈ÷ ÇÊ¿äÇÑ °æ¿ì¸¦ Á¦¿ÜÇϰí Ç÷縣ºñÇÁ·ÎÆæÀ» »ç¿ëÇØ¼´Â ¾ÈµÇ¸ç, Ä¡·á»óÀÇ À¯ÀͼºÀÌ À§Ç輺À» »óȸ[¿ôµº]ÇÑ´Ù°í ÆÇ´ÜµÉ °æ¿ì¿¡¸¸ Åõ¿©ÇÑ´Ù. »ç¿ëÇÏ´Â °æ¿ì º¹¿ë·®À» ³·°Ô À¯ÁöÇϰí Ä¡·á ±â°£À» ÃÖ´ëÇÑ Âª°Ô À¯ÁöÇÑ´Ù.
ÀӽŠÁ¦ 3 »ïºÐ±â µ¿¾È Ç÷縣ºñÇÁ·ÎÆæÀ» Æ÷ÇÔÇÑ ÇÁ·Î½ºÅ¸±Û¶õµò ÇÕ¼ºÈ¿¼Ò ¾ïÁ¦Á¦¸¦ Àü½ÅÀûÀ¸·Î »ç¿ëÇϸé žƿ¡°Ô ½ÉÆó ¹× ½ÅÀå µ¶¼ºÀ» À¯¹ßÇÒ ¼ö ÀÖÀ¸¸ç, ÀӽЏ»±â¿¡´Â »ê¸ð¿Í ¾ÆÀÌ ¸ðµÎ ÃâÇ÷ ½Ã°£ÀÌ ±æ¾îÁö°í ÁøÅëÀÌ Áö¿¬µÉ ¼ö ÀÖ´Ù. µû¶ó¼ Ç÷縣ºñÇÁ·ÎÆæÀº ÀӽŠÈı⿡´Â Åõ¿©ÇÏÁö ¾Ê´Â´Ù.
¼Ò¾Æ¿¡ ´ëÇÑ Åõ¿©
¼Ò¾Æ¿¡´Â ¾ÈÀü¼ºÀÌ È®¸³µÇ¾î ÀÖÁö ¾Ê´Ù(»ç¿ë°æÇèÀÌ Àû´Ù)
°í·ÉÀÚ¿¡ ´ëÇÑ Åõ¿©
°í·ÉÀÚ(³ëÀÎ)¿¡´Â ÀÌ ¾àÀÇ ºÎÂø ºÎÀ§ÀÇ ÇǺλóä¿¡ ÁÖÀÇÇÏ¸ç ½ÅÁßÈ÷ Åõ¿©ÇÑ´Ù.
Àû¿ë»óÀÇ ÁÖÀÇ
1) ¼Õ»óµÈ ÇÇºÎ¿Í Á¡¸·¿¡´Â »ç¿ëÇÏÁö ¾Ê´Â´Ù.
2) ½ÀÁø ¶Ç´Â ¹ßÁøºÎÀ§¿¡´Â »ç¿ëÇÏÁö ¾Ê´Â´Ù.
3) Àû¿ëºÎÀ§ÀÇ ¶¡À» ´Û¾Æ³½ ÈÄ »ç¿ëÇÑ´Ù.
º¸°ü ¹× Ãë±Þ»óÀÇ ÁÖÀÇ
±â¹Ð¿ë±â, ½Ç¿Â(1¢¦30¡É)º¸°ü
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 : Dµî±Þ
(ÀӽŠ3±â ȤÀº Ãâ»êÀÌ °¡±î¿î ½ÃÁ¡¿¡ Åõ¿©µÉ °æ¿ì )
*
»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¸°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
Flurbiprofen¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ The antiinflammatory effect of flurbiprofen may result from the reversible inhibition of cyclooxygenase, causing the peripheral inhibition of prostaglandin synthesis. Flurbiprofen also inhibits the migration of leukocytes into sites of inflammation and prevents the formation of thromboxane A2, an aggregating agent, by the platelets.
Pharmacology
Flurbiprofen¿¡ ´ëÇÑ Pharmacology Á¤º¸ Flurbiprofen, a nonsteroidal antiinflammatory drug (NSAID) of the propionic acid class, is used for the relief of pain and inflammation associated with rheumatoid arthritis and osteoarthritis and for the inhibition of intraoperative miosis. Flurbiprofen exhibits antiinflammatory, analgesic, and antipyretic activities.
Metabolism
Flurbiprofen¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 2C9 (CYP2C9)
Protein Binding
Flurbiprofen¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ > 99%
Half-life
Flurbiprofen¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 4.7-5.7 hours
Absorption
Flurbiprofen¿¡ ´ëÇÑ Absorption Á¤º¸ The mean oral bioavailability of flurbiprofen from tablets is 96% relative to an oral solution.
Pharmacokinetics
FlurbiprofenÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
ÀÛ¿ë¹ßÇö½Ã°£ : 1-2 ½Ã°£ À̳»
Biotransformation
Flurbiprofen¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic. Cytochrome P450 2C9 plays an important role in the metabolism of flurbiprofen to its major metabolite, 4¡¯-hydroxy-flurbiprofen. The 4¡¯-hydroxy-flurbiprofen metabolite showed little anti-inflammatory activity in animal models of inflammation.
Toxicity
Flurbiprofen¿¡ ´ëÇÑ Toxicity Á¤º¸ LD50 =10 mg/kg (orally in dogs).
Drug Interactions
Flurbiprofen¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Alendronate Increased risk of gastric toxicityMethotrexate The NSAID increases the effect and toxicity of methotrexateAnisindione The NSAID increases the anticoagulant effectDicumarol The NSAID increases the anticoagulant effectAcenocoumarol The NSAID increases the anticoagulant effectWarfarin The NSAID increases the anticoagulant effectCyclosporine Monitor for nephrotoxicity
CYP450 Drug Interaction
[CYP450 TableÁ÷Á¢Á¶È¸]
Food Interaction
Flurbiprofen¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take with food to reduce irritation.Avoid alcohol.
Drug Target
[Drug Target]
Description
Flurbiprofen¿¡ ´ëÇÑ Description Á¤º¸ An anti-inflammatory analgesic and antipyretic of the phenylalkynoic acid series. It has been shown to reduce bone resorption in periodontal disease by inhibiting carbonic anhydrase. [PubChem]
Dosage Form
Flurbiprofen¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Capsule, extended release OralLiquid OphthalmicTablet Oral
Drug Category
Flurbiprofen¿¡ ´ëÇÑ Drug_Category Á¤º¸ AnalgesicsAnti-Inflammatory Agents, Non-SteroidalAnti-inflammatory AgentsCarbonic Anhydrase InhibitorsCyclooxygenase InhibitorsNonsteroidal Antiinflammatory Agents (NSAIDs)
Smiles String Canonical
Flurbiprofen¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC(C(O)=O)C1=CC(F)=C(C=C1)C1=CC=CC=C1
Smiles String Isomeric
Flurbiprofen¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ C[C@@H](C(O)=O)C1=CC(F)=C(C=C1)C1=CC=CC=C1
InChI Identifier
Flurbiprofen¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C15H13FO2/c1-10(15(17)18)12-7-8-13(14(16)9-12)11-5-3-2-4-6-11/h2-10H,1H3,(H,17,18)/f/h17H
Chemical IUPAC Name
Flurbiprofen¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 2-(3-fluoro-4-phenylphenyl)propanoic acid
»ç¿ëÀÚÄÁÅÙÃ÷
ÃÖ±ÙÁ¤º¸¼öÁ¤ÀÏ 2025-06-05
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