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¿¡Æú¹ÎīŸÇö󽺸¶(150.4mg) [diclofenac epolamine]
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µå·°ÀÎÆ÷¿¡¼´Â ÀǾàǰ ÀÎÅÍ³Ý ÆÇ¸Å¸¦ ÇÏÁö ¾Ê½À´Ï´Ù. |
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ÀÌ¿ëÇÏ½Ç ¼ö ÀÖ½À´Ï´Ù.
À¯·áÁ¤º¸¸ñ·ÏÀº Àü¹®È¸¿øÀ¸·Î
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û±¸ÄÚµå(KDÄÚµå) ºñ±Þ¿©Á¡°ËÄÚµå »óÇÑ±Ý¾× |
[A67301012]
[º¸ÇèÄڵ忡 µû¸¥ ¾àǰ±âº»Á¤º¸ Á÷Á¢Á¶È¸]
\0 ¿ø/§²/¸Å(2007.08.01)(ÇöÀç¾à°¡)
\342 ¿ø/§²/¸Å(2006.08.01)(º¯°æÀü¾à°¡)
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Èò»ö ¶Ç´Â ´ãȲ»öÀÇ Á¡Âø¼ºÀÇ ´Ï»óÀÇ °íü¸¦ ºÎÁ÷Æ÷À§¿¡ µµÆ÷ÇÑ Æ¯ÀÌÇÑ ÇâÀ» °¡Áø īŸÇö󽺸¶Á¦ [Á¦ÇüÁ¤º¸ È®ÀÎ] |
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1) »ó¿Ï°ñ »ó°ú¿°(Å״Ͻº¿¤º¸¿ì µî)
2) ¿Ü»ó¼º ¿°Áõ : Ÿ¹Ú»ó, »ã(¿°ÁÂ)
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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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- »ó¿Ï°ñ »ó°ú¿° : 1ȸ 1¸Å, 1ÀÏ 2ȸ(¾ÆÄ§, Àú³á) ȯºÎ¿¡ ºÎÂøÇÏ¿© »ç¿ëÇÑ´Ù(ÃÖ´ë 14ÀÏ À̳»·Î »ç¿ëÇÑ´Ù).
- Ÿ¹Ú»ó, »ã(¿°ÁÂ) : 1ȸ 1¸Å, 1ÀÏ 1ȸ ȯºÎ¿¡ ºÎÂøÇÏ¿© »ç¿ëÇÑ´Ù(ÃÖ´ë 3ÀÏ À̳»·Î »ç¿ëÇÑ´Ù).
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1) ÀÌ ¾à ¹× ÀÌ ¾à ¼ººÐ¿¡ °ú¹Î¹ÝÀÀ ¶Ç´Â ±× º´·ÂÀÌ Àִ ȯÀÚ
2) ¾Æ½ºÇǸ° ¶Ç´Â ±âŸÀÇ ºñ½ºÅ×·ÎÀ̵å¼Ò¿°ÁøÅëÁ¦¿¡ °ú¹Î¹ÝÀÀ ȯÀÚ
3) ¾Æ½ºÇǸ° ¶Ç´Â ±âŸÀÇ ºñ½ºÅ×·ÎÀ̵å¼Ò¿°ÁøÅëÁ¦¿¡ ´ëÇÑ Ãµ½Ä(ºñ½ºÅ×·ÎÀ̵å¼Ò¿°ÁøÅëÁ¦ µî¿¡ ÀÇÇÑ Ãµ½Ä ¹ßÀÛÀ» À¯¹ß) ¶Ç´Â ±× º´·ÂÀÌ Àִ ȯÀÚ(õ½Ä ¹ßÀÛÀ» ÀÏÀ¸Å³ ¼ö ÀÖ´Ù)
4) ÀӽŠ5°³¿ùÀÌ °æ°úÇÑ ÀÓºÎ
5) ¼öÀ¯ºÎ
6) 16¼¼ ¹Ì¸¸ÀÇ ¼Ò¾Æ
7) º´º¯ÀÌ ÀÖ´Â ÇǺÎ(»ïÃâÇǺο°, ½ÀÁø, °¨¿°µÈ º´º¯, È»ó, »óó µî)¿¡´Â »ç¿ëÇÏÁö ¸» °Í.
8) ¼Òȱ˾çȯÀÚ
9) °ü»óµ¿¸Æ¿ìȸ¼ú ¼ö¼ú ȯÀÚ |
| ½ÅÁßÅõ¿© |
1) ±â°üÁö õ½Ä ȯÀÚ(ÁßÁõ õ½Ä¹ßÀÛÀ» ÀÏÀ¸Å³ ¼ö ÀÖ´Ù)
2) ÇǺÎÀÇ °¨¿°ÁõÀ» ºÒÇö¼ºÈÇÒ ¿ì·Á°¡ ÀÖÀ¸¹Ç·Î °¨¿°À» ¼ö¹ÝÇÏ´Â ¿°Áõ¿¡ ´ëÇØ ÀÌ ¾àÀ» »ç¿ëÇÏ´Â °æ¿ì¿¡´Â ÀûÀýÇÑ Ç×±ÕÁ¦ ¶Ç´Â Ç×Áø±ÕÁ¦¸¦ º´¿ëÇϰí ÃæºÐÈ÷ °üÂûÇÏ¿© ½ÅÁßÈ÷ Åõ¿©ÇÒ °Í.
3) ¸¸¼ºÁúȯ(ÅðÇ༺°üÀý¿°(°ñ°üÀý¿°) µî)¿¡ ÀÌ ¾àÀ» »ç¿ëÇÏ´Â °æ¿ì¿¡´Â ¾à¹°¿ä¹ý ÀÌ¿ÜÀÇ ¿ä¹ýµµ °í·ÁÇÑ´Ù. ¶Ç ȯÀÚ »óŸ¦ ÃæºÐÈ÷ °üÂûÇϰí ÀÌ»ó¹ÝÀÀ ¹ßÇö¿¡ À¯ÀÇÇÒ °Í.
4) ÀӺΠ: ÀÌ ¾àÀ» ÀӽűⰣ Áß¿¡ »ç¿ëÇÑ °æÇèÀº ÃæºÐÇÏÁö ¾Ê´Ù. µ¿¹° ½ÇÇè¿¡¼ »ý½Äµ¶¼ºÀÌ ÀÖ´Â °ÍÀ¸·Î ¾Ë·ÁÁ³´Ù. »ç¶÷¿¡ ´ëÇÑ À§Ç輺¿©ºÎ´Â ¾Ë·ÁÁ® ÀÖÁö ¾Ê´Ù. µû¶ó¼ ÀÌ ¾àÀ» ÀӽŠ1±â ¹× 2±â¿¡ »ç¿ëÇÏ¿©¼´Â ¾ÈµÇ°í, ÀӽŠ5°³¿ù ÀÌÈÄÀÇ ÀÓ»êºÎ¿¡¼´Â ±Ý±âÀÌ´Ù.
ÀӽŠ3±â¿¡ ÇÁ·Î½ºÅ¸±Û¶õµò ÇÕ¼º ¾ïÁ¦Á¦¸¦ »ç¿ëÇÏ´Â °æ¿ì, ÀڱüöÃàÀ» ÀúÇØÇϰí ÀӽŠ¹× ºÐ¸¸ÀÌ Áö¿¬µÉ ¼ö ÀÖ°í, ½Å»ý¾ÆÀÇ ½ÉÆóµ¶¼º(µ¿¸Æ°ü Á¶±â Æó¼â¸¦ ¼ö¹ÝÇÏ´Â Æó°íÇ÷¾Ð), ¾ç¼ö°ú¼ÒÁõÀ» ¼ö¹ÝÇÏ´Â ½Å»ý¾ÆÀÇ ½Å±â´ÉÀúÇÏ, »ê¸ð ¹× ½Å»ý¾ÆÀÇ ÃâÇ÷ ¹× »ê¸ðÀÇ ºÎÁ¾ µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°ÁøÅëÁ¦(NSAIDs)´Â ÇÁ·Î½ºÅ¸±Û¶õµò ¸Å°³ ÀÛ¿ë±âÀüÀ¸·Î ÀÎÇØ ³Æ÷ÆÄ¿À» ¹æÇØÇϰųª Áö¿¬½Ãų ¼ö ÀÖÀ¸¸ç, ÀÌ´Â ÀϺΠ¿©¼º¿¡°Ô °¡¿ªÀû ºÒÀÓÀ» ÀÏÀ¸Å³ ¼ö ÀÖ´Ù. µû¶ó¼ ÀÓ½ÅÀÌ ¾î·Æ°Å³ª ºÒÀӰ˻縦 ¹Þ°í ÀÖ´Â ¿©¼ºÀÇ °æ¿ì ÀÌ ¾àÀ» Æ÷ÇÔÇÑ NSAIDs °è¿ ¾à¹°ÀÇ »ç¿ëÁß´ÜÀ» °í·ÁÇØ¾ß ÇÑ´Ù.
5) ¼öÀ¯ºÎ: ¸ðÀ¯ÁßÀ¸·ÎÀÇ ÀÌÇàÀÌ º¸°íµÇ¾î ÀÖÀ¸¸ç, ÀÌ·Î ÀÎÇØ ¿µ¾Æ¿¡¼ ½É°¢ÇÑ ÀÌ»ó¹ÝÀÀÀÇ ¹ß»ýÀÌ ¿ì·ÁµÇ¹Ç·Î, ¼öÀ¯ºÎ¿¡ ´ëÇÑ ¾à¹° Åõ¿©¸¦ °í·ÁÇØ¾ß ÇÑ´Ù.
6) Àü½Å¿¡ ³ªÅ¸³ª´Â È¿°ú´Â ³·À» °ÍÀ¸·Î ¿¹»óµÇ³ª ½ÅÀå, ½ÉÀå(¿ïÇ÷½ÉºÎÀü µî) ¶Ç´Â °£Àå¾Ö ȯÀÚ, ¼Òȼº±Ë¾ç, À§Àå°ü ÃâÇ÷¡¤Ãµ°ø ¶Ç´Â ¿°ÁõâÀÚº´, ÃâÇ÷üÁú º´·ÂÀÌ Àִ ȯÀÚ¿¡´Â ½ÅÁßÈ÷ »ç¿ëÇÑ´Ù.
7) °í·É ȯÀÚÀÇ °æ¿ì ¿¬·ÉÀÌ ³·Àº ȯÀÚº¸´Ù NSAIDs °ü·Ã ÁßÁõ ½ÉÇ÷°ü°è, À§Àå°ü, ¹×/¶Ç´Â ½ÅÀå ÀÌ»ó ¹ÝÀÀÀÇ À§Ç輺ÀÌ ´õ ³ô´Ù. °í·ÉÀÚ¿¡ ÀÖ¾î¼ ÇÊ¿äÇÑ ÃÖ¼Ò·®À¸·Î ½ÅÁßÈ÷ Åõ¿©Çϰí ÀÌ»ó¹ÝÀÀ ¹ßÇö¿¡ ƯÈ÷ À¯ÀÇÇÑ´Ù.
8) ÀÌ ¾àÀº ÆÄ¶ó¿Á½Ãº¥Á¶»ê¸ÞÆ¿ ¹× ÆÄ¶ó¿Á½Ãº¥Á¶»êÇÁ·ÎÇÊÀ» ÇÔÀ¯Çϰí ÀÖ¾î ¾Ë·¹¸£±â¹ÝÀÀÀ» ³ªÅ¸³¾ ¼ö ÀÖÀ¸¹Ç·Î ÁÖÀÇÇÑ´Ù.
9) ¾Ë·¹¸£±â Áúȯ ȯÀÚ¿¡¼ ±â°üÁö¿¬ÃàÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
10) °íÇ÷¾Ð, ºÎÁ¾ ȯÀÚ
11) ÀÌ ¾àÀº ÇÁ·ÎÇÊ·»±Û¸®ÄÝÀ» ÇÔÀ¯Çϰí ÀÖÀ¸¹Ç·Î ÀÌ ¼ººÐ¿¡ °ú¹ÎÇϰųª ¾Ë·¹¸£±â º´·ÂÀÌ Àִ ȯÀÚ¿¡°Ô ½ÅÁßÈ÷ Åõ¿©ÇÑ´Ù. |
| ÀÌ»ó¹ÝÀÀ |
´ÙÀ½°ú °°Àº °æ¿ì ÀÌ ¾àÀÇ »ç¿ëÀ» Áï°¢ ÁßÁöÇϰí ÀÇ»ç, Ä¡°úÀÇ»ç, ¾à»ç¿Í »óÀÇÇÒ °Í. »ó´ã½Ã °¡´ÉÇÑÇÑ ÀÌ Ã·ºÎ ¹®¼¸¦ ¼ÒÁöÇÒ °Í.
1) ÇǺΠ: °¡·Á¿ò, ºÓÀ½, È«¹Ý, ¹ßÁø, Àû¿ëºÎÀ§ÀÇ ¹ÝÀÀ, ¾Ë·¹¸£±âÇǺο°, ¹ÚÅ»ÇǺο°, ½ºÆ¼ºì½¼-Á¸½¼ÁõÈıº, µ¶¼ºÇ¥ÇDZ«»ç¿ëÇØ°¡ ³ªÅ¸³ª´Â °æ¿ì
2) °ú¹Î¹ÝÀÀ : µå¹°°Ô ¾Æ³ªÇʶô½Ã½º¸ð¾çÁõ»ó (µÎµå·¯±â, È£Èí°ï¶õ µî)ÀÌ ³ªÅ¸³ª´Â °æ¿ì
3) ±ÇÀå ±â°£ µ¿¾È »ç¿ëÇÑ ÈÄ¿¡µµ Áõ»óÀÌ °³¼±µÇÁö ¾Ê´Â °æ¿ì
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ÀÌ ¾àÀ» »ç¿ëÇÏ´Â µ¿¾È ´ÙÀ½ÀÇ ¾àÀ» º¹¿ëÇÏÁö ¸» °Í.
µðŬ·ÎÆä³« Á¦Á¦³ª ºñ½ºÅ×·ÎÀ̵å¼Ò¿°ÁøÅëÁ¦¸¦ ±¹¼ÒÀûÀ¸·Î Àû¿ëÇϰųª º¹¿ëÇÏÁö ¸» °Í. |
| Off-label Usage |
[Á¶È¸]
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| Related FDA Approved Drug |
±âÁØ ¼ººÐ: DICLOFENAC EPOLAMINEFLECTOR (DICLOFENAC EPOLAMINE)
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(diclofenac sodium )
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»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.
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| DUR (ÀǾàǰ»ç¿ëÆò°¡) |
º´¿ë±Ý±â :
°í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
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|
| Mechanism of Action |
diclofenac¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ The antiinflammatory effects of diclofenac are believed to be due to inhibition of both leukocyte migration and the enzyme cylooxygenase (COX-1 and COX-2), leading to the peripheral inhibition of prostaglandin synthesis. As prostaglandins sensitize pain receptors, inhibition of their synthesis is responsible for the analgesic effects of ketoprofen. Antipyretic effects may be due to action on the hypothalamus, resulting in peripheral dilation, increased cutaneous blood flow, and subsequent heat dissipation.
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| Pharmacology |
diclofenac¿¡ ´ëÇÑ Pharmacology Á¤º¸ Diclofenac is an acetic acid nonsteroidal antiinflammatory drug (NSAID) with analgesic and antipyretic properties. Diclofenac is used to treat pain, dysmenorrhea, ocular inflammation, osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, and actinic keratosis
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| Absorption |
diclofenac¿¡ ´ëÇÑ Absorption Á¤º¸ Completely absorbed from the gastrointestinal tract.
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| Pharmacokinetics |
diclofenac epolamineÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- ´Ü¹é°áÇÕ : 99%
- ´ë»ç : °£¿¡¼ ºñȰ¼ºÇü ´ë»çü·Î ´ë»çµÊ
- ¹Ý°¨±â : 2½Ã°£
- Ç÷ÁßÃÖ°í³óµµ µµ´Þ½Ã°£ : 1-2 ½Ã°£ À̳»
- ¼Ò½Ç : ÁÖ·Î ½Å¹è¼³
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| Toxicity |
diclofenac¿¡ ´ëÇÑ Toxicity Á¤º¸ Symptoms of overdose include loss of consciousness, increased intracranial pressure, and aspiration pneumonitis. LD50=390mg/kg (orally in mice)
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| Drug Interactions |
diclofenac¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Alendronate Increased risk of gastric toxicityAnisindione The NSAID increases the anticoagulant effectCyclosporine Monitor for nephrotoxicityDicumarol The NSAID increases the anticoagulant effectWarfarin The NSAID increases the anticoagulant effectRifampin Decreased levels/effect of the NSAID
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸] diclofenac¿¡ ´ëÇÑ P450 table
SUBSTRATES
CYP 2C9
NSAIDs:
**diclofenac**
ibuprofen
piroxicam
Oral Hypoglycemic Agents:
tolbutamide
glipizide
Angiotensin II Blockers:
NOT candesartan
irbesartan
losartan
NOT valsartan
celecoxib
fluvastatin naproxen
phenytoin
sulfamethoxazole
tamoxifen
tolbutamide
torsemide
warfarin
INHIBITORS
CYP 2C9
amiodarone
fluconazole
isoniazid
INDUCERS
CYP 2C9
rifampin
secobarbital
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| Drug Target |
[Drug Target]
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| Description |
diclofenac¿¡ ´ëÇÑ Description Á¤º¸ A non-steroidal anti-inflammatory agent (NSAID) with antipyretic and analgesic actions. It is primarily available as the sodium salt. [PubChem]
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| Dosage Form |
diclofenac¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Solution OphthalmicSolution TopicalSuppository RectalTablet OralTablet, coated OralTablet, extended release Oral
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| Drug Category |
diclofenac¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Inflammatory Agents, Non-SteroidalCyclooxygenase InhibitorsNonsteroidal Antiinflammatory Agents (NSAIDs)
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| Smiles String Canonical |
diclofenac¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ OC(=O)CC1=CC=CC=C1NC1=C(Cl)C=CC=C1Cl
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| Smiles String Isomeric |
diclofenac¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ OC(=O)CC1=CC=CC=C1NC1=C(Cl)C=CC=C1Cl
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| InChI Identifier |
diclofenac¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C14H11Cl2NO2/c15-10-5-3-6-11(16)14(10)17-12-7-2-1-4-9(12)8-13(18)19/h1-7,17H,8H2,(H,18,19)/f/h18H
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| Chemical IUPAC Name |
diclofenac¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 2-[2-[(2,6-dichlorophenyl)amino]phenyl]acetic acid
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| Drug-Induced Toxicity Related Proteins |
DICLOFENAC ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸ Replated Protein:CYP3A4 Drug:Diclofenac Toxicity:idiosyncratic hepatotoxicity. [¹Ù·Î°¡±â] Replated Protein:CYP2C9 Drug:Diclofenac Toxicity:idiosyncratic hepatotoxicity. [¹Ù·Î°¡±â]
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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