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¿µÁø¼¼Æ÷Æä¶óÁ¸ÁÖ2.0g CEFOPERAZONE INJ. 2G YOUNGJIN[Cefoperazone Sodium]
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¡Û ¼ºÀÎ : ¼¼Æ÷Æä¶óÁ¸À¸·Î¼ 1ÀÏ 2 ¢¦ 4 g(¿ª°¡)À» 12½Ã°£¸¶´Ù ºÐÇÒÇÏ¿© Á¤¸Æ ¶Ç´Â ±ÙÀ°ÁÖ»ç ÇÑ´Ù.
ÁßÁõ ¶Ç´Â °¨¼ö¼ºÀÌ ³·Àº ±ÕÁÖ¿¡ ÀÇÇÑ °¨¿°Áõ : ÀÌ ¾àÀ¸·Î¼ 1ÀÏ 6 ¢¦ 12 g(¿ª°¡)À» 2 ¢¦ 4ȸ ºÐÇÒ 1ȸ 1.5 ¢¦ 4 g(¿ª°¡)À¸·Î Åõ¿©ÇÑ´Ù.
¡Û À¯¼Ò¾Æ : ÀÌ ¾àÀ¸·Î¼ 1ÀÏ Ã¼Áß kg´ç 25 ¢¦ 150 mg(¿ª°¡)À» 2 ¢¦ 4ȸ ºÐÇÒÇÏ¿© Á¤¸ÆÁÖ»çÇÑ´Ù.
¡Û ½ÅºÎÀü ȯÀÚ : Å©·¹¾ÆÆ¼´Ñû¼ÒÀ²ÀÌ 18 mL/minº¸´Ù Àû°Å³ª, Ç÷ûũ·¹¾ÆÆ¼´ÑÄ¡°¡ 3.5 mg/dLº¸´Ù Å« ȯÀÚ¿¡ ´ëÇÑ ÃÖ´ë¿ë·®Àº 1ÀÏ 4 g(¿ª°¡)ÀÌ´Ù.
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Á¤¸ÆÁÖ»ç ½Ã´Â 5 %, 10 % Æ÷µµ´ç ÁÖ»ç¾×, 5 % Æ÷µµ´çÁÖ»ç¾×°ú »ý¸®½Ä¿° ÁÖ»ç¾×ÀÇ È¥ÇÕ¾×, »ý¸®½Ä¿° ÁÖ»ç¾×, 5 % Æ÷µµ´ç ÁÖ»ç¾×°ú 0.2 % ¿°È³ªÆ®·ýÁÖ»ç¾×ÀÇ È¥ÇÕ¾× µîÀ» Èñ¼®¾×À¸·Î »ç¿ëÇϰí, Á¡Àû Á¤¸ÆÁÖ»ç ½Ã´Â 5 % ¶Ç´Â 10 % Æ÷µµ´çÁÖ»ç¾×, 5 % Æ÷µµ´çÁÖ»ç¾×°ú À¯»ê¿°¸µ°ÖÁÖ»ç¾×, 5 % Æ÷µµ´çÁÖ»ç¾×°ú »ý¸®½Ä¿° ÁÖ»ç¾×ÀÇ È¥ÇÕ¾×, »ý¸®½Ä¿° ÁÖ»ç¾×, 5 % Æ÷µµ´çÁÖ»ç¾×°ú 0.2 % ¿°È³ªÆ®·ýÁÖ»ç¾×ÀÇ È¥ÇÕ¾× µîÀ» »ç¿ëÇÑ´Ù.
1. Á¤¸ÆÁÖ»ç
1) Á÷Á¢ Á¤¸ÆÁÖ»ç : ÃÖ´ë·®Àº ¼ºÀÎÀÇ °æ¿ì 1ȸ 2 g(¿ª°¡), ¼Ò¾ÆÀÇ °æ¿ì üÁß kg´ç 50 mg(¿ª°¡)À» ³ÑÁö ¾Ê¾Æ¾ß ÇÑ´Ù. ÃÖÁ¾³óµµ°¡ 100 mg/mLÀÌ µÇµµ·Ï Àû´çÇÑ Èñ¼®¾×¿¡ ³ì¿© 3 ¢¦ 5ºÐ°£¿¡ °ÉÃÄ Á¤¸ÆÁÖ»ç ÇÑ´Ù.
2) °£ÇæÁ¡Àû Á¤¸ÆÁÖ»ç : ÀÌ ¾à 1 g(¿ª°¡) ¶Ç´Â 2 g(¿ª°¡)À» Èñ¼®¾×(1 g´ç 5 mL)¿¡ ³ìÀÎ ÈÄ, 20 ¢¦ 40 mLÀÇ Á¡Àû Á¤¸ÆÁÖ»ç¿ë¾×¿¡ È¥ÇÕÇÏ¿© 15ºÐ ¢¦ 1½Ã°£¿¡ °ÉÃÄ ÁÖ»çÇÑ´Ù.
3) Áö¼ÓÁ¡Àû Á¤¸ÆÁÖ»ç : 1 g(¿ª°¡)´ç ÁÖ»ç¿ë¼ö 5 mL¿¡ ³ìÀÎ ÈÄ Àû´çÇÑ Á¡Àû Á¤¸ÆÁÖ»ç¿ë¾×¿¡ ³ì¿© ÃÖÁ¾³óµµ°¡ 2 ¢¦ 25 mg/mL·Î ÇÏ¿© ÁÖ»çÇÑ´Ù.
2. ±ÙÀ°ÁÖ»ç
ÁÖ»ç¿ë¼ö¿¡ ³ì¿© ÁÖ»çÇϰí 250 mg/mL ÀÌ»óÀ» ±ÙÀ°ÁÖ»ç ÇÒ ¶§´Â 0.5 % ¸®µµÄ«ÀÎ ÁÖ»ç¾×¿¡ ³ì¿© ±ÙÀ°ÁÖ»çÇÑ´Ù.
Èñ¼®¹ýÀº ´ÙÀ½ Ç¥¿Í °°´Ù. ¸ÕÀú ÀÌ ¾àÀ» ÁÖ»ç¿ë¼ö Çʿ䷮¿¡ ³ìÀÎ ÈÄ 2 % ¸®µµÄ«ÀÎ Çʿ䷮À» °¡ÇÏ¿© 0.5 % ¸®µµÄ«ÀÎ ÁÖ»ç¾×À¸·Î ÇÏ¿© ±ÙÀ°ÁÖ»çÇÑ´Ù.
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2 % ¸®µµÄ«ÀÎ
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0.25 g ¹ÙÀ̾Ë
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250 mg/mL
333 mg/mL
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0.7 mL
0.4 mL
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0.2 mL
0.2 mL
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1.0 mL
0.75 mL
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0.5 g ¹ÙÀ̾Ë
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250 mg/mL
333 mg/mL
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1.3 mL
0.9 mL
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0.4 mL
0.3 mL
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2.0 mL
1.5 mL
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1.0 g ¹ÙÀ̾Ë
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250 mg/mL
333 mg/mL
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2.6 mL
1.8 mL
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0.9 mL
0.6 mL
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4.0 mL
3.0 mL
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2.0 g ¹ÙÀ̾Ë
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250 mg/mL
333 mg/mL
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5.2 mL
3.7 mL
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1.8 mL
1.2 mL
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8.0 mL
6.0 mL
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1) ÀÌ ¾à¿¡ ÀÇÇÏ¿© ¼îÅ©ÀÇ º´·ÂÀÌ Àִ ȯÀÚ
2) ¼¼ÆÈ·Î½ºÆ÷¸°°è Ç×»ý¹°Áú¿¡ °ú¹Î¹ÝÀÀ ȯÀÚ
3) ¸®µµÄ«ÀÎ µîÀÇ ¾Æ´Ò¸®µå°è ±¹¼Ò¸¶ÃëÁ¦¿¡ °ú¹Î¹ÝÀÀÀÇ º´·ÂÀÌ Àִ ȯÀÚ(±ÙÀ°ÁÖ»ç)
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1) ÀÌ ¾à ¶Ç´Â ¼¼Æè°è Ç×»ý¹°Áú¿¡ °ú¹Î¹ÝÀÀÀÇ º´·ÂÀÌ Àִ ȯÀÚ¿¡´Â Åõ¿©ÇÏÁö ¾Ê´Â °ÍÀ» ¿øÄ¢À¸·Î Çϳª ºÎµæÀÌ Åõ¿©ÇÒ °æ¿ì¿¡´Â ½ÅÁßÈ÷ Åõ¿©ÇÑ´Ù.
2) Æä´Ï½Ç¸°°è Ç×»ý¹°Áú¿¡ °ú¹Î¹ÝÀÀÀÇ º´·ÂÀÌ Àִ ȯÀÚ
3) º»ÀÎ ¶Ç´Â ºÎ¸ð, ÇüÁ¦°¡ ±â°üÁöõ½Ä, ¹ßÁø, µÎµå·¯±â µîÀÇ ¾Ë·¹¸£±â Áõ»óÀ» ÀÏÀ¸Å°±â ½¬¿î üÁúÀΠȯÀÚ
4) ÁßÁõÀÇ °£ ¶Ç´Â ½ÅÀå¾Ö ȯÀÚ
5) ºÒ·®ÇÑ ¿µ¾ç»óÅÂ, Èí¼öÀå¾Ö »óÅÂ(¿¹, ³¶¼º¼¶À¯Áõ), ¾ËÄÚ¿Ã Áßµ¶Áõ, Àå±â°£ÀÇ °í¿µ¾çó¹æÀ» ¹Þ°í Àִ ȯÀÚ(Á¤¸Æ ¶Ç´Â ºñÀ§°üÀ» ÅëÇØ¼), °í·ÉÀÚ, Àü½Å»óŰ¡ ³ª»Û ȯÀÚ(ºñŸ¹Î K °áÇÌÁõ»óÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÃæºÐÈ÷ °üÂûÇÑ´Ù) |
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1) ¼îÅ© : ¾Æ³ªÇʶô½Ã½º µå¹°°Ô ¼îÅ©¸¦ ÀÏÀ¸Å³ ¼ö ÀÖÀ¸¹Ç·Î ÃæºÐÈ÷ °üÂûÇÏ°í ºÒÄè°¨, ±¸³»ÀÌ»ó°¨, õ¸í, ¾îÁö·³, º¯ÀÇ, À̸í, ¹ßÇÑ µîÀÇ ÀÌ»óÀÌ ³ªÅ¸³ª´Â °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇϰí ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù.
2) °ú¹Î¹ÝÀÀ : ¶§¶§·Î ¹ßÁø, ¹ÝÁ¡»ó ±¸Áø, µÎµå·¯±â, °¡·Á¿ò, ¹ß¿ µå¹°°Ô È«¹Ý µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÀÌ·¯ÇÑ Áõ»óÀÌ ³ªÅ¸³ª´Â °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇϰí ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù.
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4) È£Èí±â°è : µå¹°°Ô ¹ß¿, ±âħ, È£Èí°ï¶õ, ÈäºÎ X¼± ÀÌ»ó, È£»ê±¸ Áõ°¡ µîÀ» ¼ö¹ÝÇÏ´Â °£Áú¼º Æó·Å, È£»ê±¸¼º ÆóħÀ± µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÀÌ·¯ÇÑ Áõ»óÀÌ ³ªÅ¸³ª´Â °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇϰí ÄÚ¸£Æ¼ÄÚÀ̵å Åõ¿© µî ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù.
5) Ç÷¾×°è : ¶§¶§·Î ºóÇ÷, °ú¸³±¸ °¨¼Ò, Ç÷¼ÒÆÇ °¨¼Ò, È£»ê±¸ Áõ°¡, È£Áß±¸ °¨¼Ò, Çì¸ð±Û·Îºó °¨¼Ò, Ç츶ÅäÅ©¸´Ä¡ °¨¼Ò µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù. ´Ù¸¥ Ç×»ý¹°Áú Åõ¿© ½Ã ¿ëÇ÷¼º ºóÇ÷ÀÌ ³ªÅ¸³µ´Ù´Â º¸°í°¡ ÀÖ´Ù.
6) ÁßÃ߽Űæ°è : µå¹°°Ô °æ·ÃÀ» ÀÏÀ¸Å³ ¼ö ÀÖ´Ù.
7) ÇǺΠ: ´Ù¸¥ Ç×»ý¹°Áú Åõ¿© ½Ã ÇǺÎÁ¡¸·¾ÈÁõÈıº(½ºÆ¼ºì½º-Á¸½¼ ÁõÈıº)ÀÌ ³ªÅ¸³µ´Ù´Â º¸°í°¡ ÀÖ°í µå¹°°Ô µ¶¼ºÇ¥ÇDZ«»ç¿ëÇØ(¸®¿¤ÁõÈıº)°¡ ÀϾ ¼ö°¡ ÀÖÀ¸¹Ç·Î °üÂûÀ» ÃæºÐÈ÷ Çϰí ÀÌ»óÀÌ ÀÖÀ» °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇϰí ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù.
8) °£Àå : µå¹°°Ô Ȳ´Þ, ºô¸®·çºó »ó½Â ¶§¶§·Î AST, ALT, ALPÀÇ »ó½ÂÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÀÌ»óÀÌ ³ªÅ¸³ª´Â °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇϰí ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù.
9) ½ÅÀå : µå¹°°Ô ±Þ¼º ½ÅºÎÀü µîÀÇ ÁßÁõÀÇ ½ÅÀå¾Ö°¡ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î Á¤±âÀûÀ¸·Î °Ë»ç¸¦ ½Ç½ÃÇÏ´Â µî ÃæºÐÈ÷ °üÂûÇϰí ÀÌ»óÀÌ ÀÎÁ¤µÇ´Â °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇϰí ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù.
10) ±Õ±³´ëÁõ : µå¹°°Ô ±¸³»¿°, ĵð´ÙÁõÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
11) ºñŸ¹Î°áÇÌÁõ : µå¹°°Ô ºñŸ¹Î K °áÇÌÁõ»ó(ÀúÇÁ·ÎÆ®·ÒºóÇ÷Áõ, ÃâÇ÷°æÇâ µî), ºñŸ¹Î B±º °áÇÌÁõ»ó(Çô¿°, ±¸³»¿°, ½Ä¿åºÎÁø, ½Å°æ¿° µî)ÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
12) ±âŸ : µå¹°°Ô µÎÅë, ºÎÁ¾, ±Çۨ, Ȳö°Å¸²ÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
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1) Ǫ·Î¼¼¹Ìµå µîÀÇ ÀÌ´¢Á¦³ª ¾Æ¹Ì³ë±Û¸®ÄÚ»çÀ̵å°è Ç×»ý¹°Áú°ú º´¿ëÅõ¿© ½Ã ½ÅÀå¾Ö°¡ Áõ°¡µÉ ¼ö ÀÖÀ¸¹Ç·Î ½ÅÁßÈ÷ Åõ¿©ÇÑ´Ù.
2) ¾ËÄÚ¿Ã, Ç׺ñŸ¹Î K Á¦Á¦, °£µ¶¼º ¾à¹°°úÀÇ º´¿ëÅõ¿© ½Ã ÁÖÀÇÇÑ´Ù. |
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±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. |
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| º¸°ü»ó ÁÖÀÇ |
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| Ç׸ñ |
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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 |
Cefoperazone¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Like all beta-lactam antibiotics, cefoperazone binds to specific penicillin-binding proteins (PBPs) located inside the bacterial cell wall, causing the inhibition of the third and last stage of bacterial cell wall synthesis. Cell lysis is then mediated by bacterial cell wall autolytic enzymes such as autolysins.
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| Pharmacology |
Cefoperazone¿¡ ´ëÇÑ Pharmacology Á¤º¸ Cefoperazone is a third generation cephalosporin antibiotic. Cefoperazone exerts its bactericidal effect by inhibiting the bacterial cell wall synthesis
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| Protein Binding |
Cefoperazone¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ The degree of reversible protein binding varies with the serum concentration from 93% at 25 mcg/mL to 90% at 250 mcg/mL and 82% at 500 mcg/mL.
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| Half-life |
Cefoperazone¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ The mean serum half-life is approximately 2.0 hours, independent of the route of administration.
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| Pharmacokinetics |
Cefoperazone SodiumÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
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- ´ëºÎºÐÀÇ Ã¼³» Á¶Á÷ ¹× ü¾×¿¡ ³Î¸® ºÐÆ÷ÇÑ´Ù.
- ´ãÁó¿¡ °¡Àå °í³óµµ·Î ºÐÆ÷ÇÑ´Ù.
- ³úô¼ö¾×¿¡´Â °ÅÀÇ ºÐÆ÷ÇÏÁö ¾Ê´Â´Ù.
- ¼ö¸·¿¡ ¿°ÁõÀÌ ÀÖ´Â °æ¿ì¿¡´Â ºÐÆ÷µÇ´Â Á¤µµ´Â ´Ù¾çÇÏ´Ù.
- ÅÂ¹Ý Åë°ú, À¯Áó ºÐºñ
- ¹Ý°¨±â : 2½Ã°£ (°£Áúȯ, ´ãÁó Æó¼â°¡ ÀÖ´Â °æ¿ì ±æ¾îÁø´Ù.)
- Ç÷ÁßÃÖ°í³óµµ µµ´Þ½Ã°£ :
- ±ÙÀ°ÁÖ»ç : 1-2 ½Ã°£ À̳»
- Á¤¸ÆÁÖ»ç : 15-20 ºÐ (Ç÷Áß³óµµ´Â ±ÙÀ°ÁÖ»ç½Ãº¸´Ù 2-3 ¹è ´õ ³ô´Ù.)
- ¼Ò½Ç : ÁÖ·Î ´ãÁó (70-75%)À» ÅëÇØ ¹è¼³µÇ¸ç, 6-12 ½Ã°£ À̳»¿¡ 20-30%°¡ ¹Ìº¯Èü·Î ½Å¹è¼³µÈ´Ù.
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| Biotransformation |
Cefoperazone¿¡ ´ëÇÑ Biotransformation Á¤º¸ No significant quanitity of metabolites have been identified in urine.
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| Toxicity |
Cefoperazone¿¡ ´ëÇÑ Toxicity Á¤º¸ Symptoms of overdose include blood in the urine, diarrhea, nausea, upper abdominal pain, and vomiting.
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| Drug Interactions |
Cefoperazone¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Drug Target |
[Drug Target]
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| Description |
Cefoperazone¿¡ ´ëÇÑ Description Á¤º¸ Semisynthetic broad-spectrum cephalosporin with a tetrazolyl moiety that is resistant to beta-lactamase. It has been proposed especially against Pseudomonas infections.
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| Smiles String Canonical |
Cefoperazone¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CCN1CCN(C(=O)NC(C(=O)NC2C3SCC(CSC4=NN=NN4C)=C(N3C2=O)C(O)=O)C2=CC=C(O)C=C2)C(=O)C1=O
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| Smiles String Isomeric |
Cefoperazone¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CCN1CCN(C(=O)N[C@@H](C(=O)N[C@H]2[C@H]3SCC(CSC4=NN=NN4C)=C(N3C2=O)C(O)=O)C2=CC=C(O)C=C2)C(=O)C1=O
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| InChI Identifier |
Cefoperazone¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C25H27N9O8S2/c1-3-32-8-9-33(21(39)20(32)38)24(42)27-15(12-4-6-14(35)7-5-12)18(36)26-16-19(37)34-17(23(40)41)13(10-43-22(16)34)11-44-25-28-29-30-31(25)2/h4-7,15-16,22,35H,3,8-11H2,1-2H3,(H,26,36)(H,27,42)(H,40,41)/t15?,16-,22-/m1/s1/f/h26-27,40H
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| Chemical IUPAC Name |
Cefoperazone¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (6R,7R)-7-[[2-[(4-ethyl-2,3-dioxopiperazine-1-carbonyl)amino]-2-(4-hydroxyphenyl)acetyl]amino]-3-[(1-methyltetrazol-5-yl)sulfanylmethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
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ÃÖ±ÙÁ¤º¸¼öÁ¤ÀÏ 2017-08-24
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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.
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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
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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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. CEFOPERAZONE[GGT Increase][Composite Activity](Score) I(Marginal) 0(Active) 0[Alkaline Phosphatase Increase](Activity Score) I(Number of Rpts) <4(Index value) 0[SGOT Increase](Activity Score) I(Number of Rpts) ¡Ã4(Index value) 0.4[SGPT Increase](Activity Score) I(Number of Rpts) <4(Index value) 0.2[LDH Increase](Activity Score) I(Number of Rpts) <4(Index value) 0.1[GGT Increase](Activity Score) I(Number of Rpts) <4(Index value) 0
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