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À¯´ÏÆÄ·Ð¿¬Áúĸ½¶(ÆÄ¹Ìµå·Ð»ê³ªÆ®·ý) [Pamidronate Disodium]
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µå·°ÀÎÆ÷¿¡¼´Â ÀǾàǰ ÀÎÅÍ³Ý ÆÇ¸Å¸¦ ÇÏÁö ¾Ê½À´Ï´Ù. |
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649503190[A50753321]
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¡Û Ä®½· ÇÔ·®ÀÇ ºÎ(ݶ)±ÕÇü¿¡ ±âÀÎÇÑ Çϱ⠰ñ´ë»ç ÀÌ»ó ÁúȯÀÇ Ä¡·á : °ñ´Ù°øÁõ
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update: 2013.05.03
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°æÁõ ¹× ÁßÁõµµÀÇ ½Å±â´É ºÎÀüȯÀÚ(Ç÷ûũ·¹¾ÆÆ¼´Ñ<5mg/dL)¿¡´Â ¿ë·®À» Á¶ÀýÇÒ ÇÊ¿ä´Â ¾øÀ¸³ª, º¸´Ù ÁßÁõÀÇ ½Å±â´É ºÎÀüȯÀÚ¿¡´Â Åõ¿©¿ë·®À» ÁÙÀ̰ųª ¹Ý°¨ÇÏ¿©¾ß ÇÑ´Ù.
¡Û °ñ´Ù°øÁõ : 1ÀÏ 200mgÀ» Áö¼ÓÀûÀ¸·Î Åõ¿©ÇÑ´Ù. 3~4³â µ¿¾ÈÀÇ Áö¼ÓÀûÀÎ Ä¡·á¿¡ ÀÇÇØ ÃÖ»óÀÇ È¿°ú¸¦ ¾òÀ» ¼ö ÀÖ´Ù. Èí¼ö°èÃø±â¸¦ »ç¿ëÇÑ ÃøÁ¤ ½Ã, Ä¡·á 1³âÈÄ À¯ÀǼº ÀÖ´Â °ñ¹Ðµµ Áõ°¡¸¦ È®ÀÎÇÒ ¼ö ÀÖÀ¸¸ç, ȯÀÚ¿¡ µû¶ó¼´Â ´õ ¿À·£ ±â°£ÀÌ ¿ä±¸µÇ±âµµ ÇÑ´Ù. ÀϺΠ½ÇÇè¿¡¼´Â 1ÀÏ 100mgÀÇ Àú¿ë·®¿¡¼µµ À¯È¿¼ºÀ» ³ªÅ¸³½´Ù.
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3) ´ëµÎÀ¯¿¡ °ú¹ÎÇϰųª ¾Ë·¹¸£±â º´·ÂÀÌ Àִ ȯÀÚ
4) Äá ¶Ç´Â ¶¥Äá¿¡ °ú¹ÎÁõÀÌ Àִ ȯÀÚ
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ÀÌ ¾à¿¡ ÀÇÇÑ ÀÌ»ó¹ÝÀÀÀº ¿ÏÈÇϰí ÀϽÃÀûÀÌ´Ù. °¡Àå ÀϹÝÀûÀÎ ÀÌ»ó¹ÝÀÀÀº °æ¹ÌÇÑ ¼ÒȺҷ® Áõ»ó¿¡¼ºÎÅÍ ±Ø½ÉÇÑ º¹Åë, ±¸¿ª, ±¸Åä¿¡ À̸£±â±îÁö ´Ù¾çÇÑ Á¤µµÀÇ ¼Òȱâ°è ÀÌ»óÀ» ÀÏÀ¸Å³ ¼ö ÀÖ´Ù. ÀÌ´Â º¸Åë Åõ¿© ùÁÖ°¿¡ ³ªÅ¸³ª´Âµ¥ ÀϽÃÀûÀ̰í Á¡Â÷ ¼Ò½ÇµÈ´Ù. ¾î¶² °æ¿ì¿¡´Â ÀϽÃÀûÀ¸·Î ¶Ç´Â ¿µ¿øÈ÷ Ä¡·á Áß´ÜÀÌ ¿ä±¸µÇ¾îÁú ¼öµµ ÀÖ´Ù. ¼Ò¼ö¿¡¼(6%) Á¡ÁøÀûÀ̰í Áö¼ÓÀûÀÎ ¹éÇ÷±¸ ¼ö °¨¼Ò°¡ ³ªÅ¸³ª´Âµ¥ Á¤»ó ¹üÀ§¸¦ ÃʰúÇÏÁö ¾Ê°í ÀϽÃÀûÀÌ°í °¡¿ªÀûÀÌ´Ù. ±×·³¿¡µµ ºÒ±¸Çϰí, ¾î¶² °æ¿ì¿¡´Â ¿¹¹æ Á¶Ä¡·Î¼ Ä¡·á Áß´ÜÀÇ Çʿ䰡 °í·ÁµÇ¾î¾ß ÇÑ´Ù.
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1) Àü½ÅÀû ÀÌ»ó¹ÝÀÀ : ÀÚÁÖ ¹ß¿, ¶§¶§·Î ±Çۨ, ¿ÀÇÑ, ÇÇ·Î, È«Á¶¸¦ ¼ö¹ÝÇÏ´Â ÀÎÇ÷翣ÀÚ¾ç ÁõÈİ¡ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
2) ±Ù °ñ°Ý°è : °ñ, °üÀý ¹×/¶Ç´Â ±ÙÀ°ÀÇ ÅëÁõ, µå¹°°Ô ±Ù°æ·Ã, ½ÉÇÑ Áõ»óÀ» µ¿¹ÝÇϰųª/µ¿¹ÝÇϰí Ȱµ¿À» ÇÒ ¼ö ¾øÀ» Á¤µµÀÇ ÅëÁõÀÌ ³ªÅ¸³² (¡®ÀϹÝÀû ÁÖÀÇ¡¯ Ç× ÂüÁ¶)
3) ¼Òȱâ°è : ¶§¶§·Î ±¸¿ª, ±¸Åä, µå¹°°Ô ½Ä¿åºÎÁø, º¹Åë, ¼³»ç, º¯ºñ, ¼ÒȺҷ® ¶ÇÇÑ ¸Å¿ì µå¹°°Ô À§¿°ÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù. ÀÌ·± °æ¿ì ÀϽÃÀûÀ¸·Î ÈÞ¾àÇϰųª Åõ¿© ÁßÁöÇÑ´Ù.
4) ÁßÃ߽Űæ°è : ¶§¶§·Î µÎÅë, µå¹°°Ô ÃÊÁ¶, È¥µ·, ºÒ¸é, Á¹À½, ¶ÇÇÑ ¸Å¿ì µå¹°°Ô ÁõÈļº ÀúÄ®½·Ç÷Áõ(Áö°¢ÀÌ»ó, Åן´Ï), ¹ßÀÛÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
5) Ç÷¾×°è : ¶§¶§·Î Àӯı¸ °¨¼Ò, ¹éÇ÷±¸ °¨¼Ò, ¶ÇÇÑ ¸Å¿ì µå¹°°Ô Ç÷¼ÒÆÇ °¨¼Ò°¡ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
6) ½É¡¤Ç÷°ü°è : µå¹°°Ô ÀúÇ÷¾Ð, °íÇ÷¾ÐÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
Á¹·¹µå·Ð»ê(4mg) ÁÖ»çÁ¦ ¹× ÆÄ¹Ìµå·Ð»ê(90mg) ÁÖ»çÁ¦¸¦ °¢°¢ Á¤¸ÆÅõ¿©ÇÑ ÈÄ È¿°ú¸¦ ºñ±³ÇÑ Àӻ󿬱¸¿¡¼ ½É¹æ¼¼µ¿ÀÇ ¹ß»ý °Ç¼ö°¡ Á¹·¹µå·Ð»ê Åõ¿©±º(3/563, 0.5%)º¸´Ù ÆÄ¹Ìµå·Ð»ê Åõ¿©±º(12/556, 2.2%)¿¡¼ ´õ ³ô°Ô ³ªÅ¸³µ´Ù. Æó°æ ÈÄ °ñ´Ù°øÁõ ȯÀÚ¸¦ ´ë»óÀ¸·Î ½Ç½ÃµÈ ÀÌÀüÀÇ ¿¬±¸¿¡¼´Â Áß´ëÇÑ À¯ÇØ»ç·Ê·Î¼ ½É¹æ¼¼µ¿ÀÇ ¹ß»ý·üÀÌ À§¾à¿¡ ºñÇØ Á¹·¹µå·Ð»ê Åõ¿©±º(5mg)¿¡¼ Áõ°¡ÇÏ´Â °ÍÀ¸·Î °üÂûµÇ¾úÀ¸³ª(0.6% ´ëºñ 1.3%), µÎ ±º°£ ½É¹æ¼¼µ¿ ¹ß»ý·ü¿¡´Â Â÷À̰¡ ¾ø¾ú´Ù. Á¹·¹µå·Ð»ê°ú ÆÄ¹Ìµå·Ð»ê Ä¡·á¿¡ ÀÇÇØ ½É¹æ¼¼µ¿ÀÇ ¹ß»ýÀÌ Áõ°¡ÇÏ´Â ±âÀü¿¡ ´ëÇØ¼´Â ¾Ë·ÁÁ® ÀÖÁö ¾Ê´Ù.
7) ½ÅÀå ºñ´¢±â°è : µå¹°°Ô ºÎÁ¾, Ç÷´¢, ±Þ¼º ½ÅºÎÀü, ½ÅÀåÁúȯÀÇ ¾ÇȰ¡ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
8) ÇǺΠ: µå¹°°Ô ¹ßÀû, °¡·Á¿òÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
9) Ư¼ö°¨°¢±â : ¸Å¿ì µå¹°°Ô Æ÷µµ¸·¿°, Ȳ½ÃÁõÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
10) »ýÈÇÐÀû º¯È : ÀúÄ®½·Ç÷Áõ, ÀúÀλêÇ÷Áõ (¾Ç¼ºÁ¾¾ç¿¡ ÀÇÇÑ °íÄ®½· ȯÀÚ¿¡¼¸¸ ÀÓ»óÀûÀ¸·Î À¯ÀÇÇÏ°Ô ³ªÅ¸³²)ÀÌ ÀÚÁÖ ³ªÅ¸³ª¸ç, ¶§¶§·Î Àú¸¶±×³×½·Ç÷Áõ, µå¹°°Ô °íÄ®·ýÇ÷Áõ, ÀúÄ®·ýÇ÷Áõ, °í³ªÆ®·ýÇ÷Áõ, ¸Å¿ì µå¹°°Ô °£±â´É °Ë»çÄ¡ ÀÌ»ó, Ç÷û Å©·¹¾ÆÆ¼´Ñ ¹× ¿ä¼ÒÄ¡ Áõ°¡°¡ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
11) ±âŸ : ¼ï, ¾Æ³ªÇʶô½Ã¾ç Áõ»ó(È£Èí°ï¶õ, õ¸í µî)ÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÀÌ·± °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇÏ´Â µî ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù.
12) ¿Ü±¹ ½ÃÆÇ ÈÄ Á¶»ç
ÀÌ ¾àÀ» Æ÷ÇÔÇÏ¿© Á¤¸ÆÁÖ»ç¿ë ºñ½ºÆ÷½ºÆ÷³×ÀÌÆ®¸¦ Åõ¿©¹ÞÀº ¾Ï ȯÀÚ¿¡¼ »À±«»ç(ÁÖ·Î ÅÎ)°¡ º¸°íµÇ¾ú´Ù. ÀÌ Áß ¸¹Àº ȯÀÚµéÀÌ ÅλÀ±«»çÀÇ À§Çè¿äÀÎÀÏ ¼ö ÀÖ´Â ÈÇпä¹ý ¹× ÄÚ¸£Æ¼ÄÚ½ºÅ×·ÎÀ̵带 º´¿ëÅõ¿©Çϰí ÀÖ¾ú´Ù. ÁøÇàµÈ À¯¹æ¾Ï ¹× ´Ù¹ß¼º°æÈÁõ°ú °°Àº ƯÁ¤ÇÑ ¾Ï¿¡¼ º¸°í ºóµµ Áõ°¡°¡ ³ªÅ¸³µ´Ù. º¸°íµÈ Áõ·Ê Áß °¡Àå ¸¹Àº °æ¿ì´Â ¾ÏȯÀÚ°¡ ¹ßÄ¡¿Í °°Àº ħ½ÀÀû Ä¡°ú ¼ö¼úÀ» ¹ÞÀº ÀÌÈÄ¿´´Ù. ȸº¹À» Áö¿¬½Ãų ¼ö ÀÖÀ¸¹Ç·Î ħ½ÀÀû Ä¡°ú ¼ö¼úÀº ÇÇÇÏ´Â °ÍÀÌ ÁÁ´Ù.
µ¿ Á¦Á¦¸¦ Æ÷ÇÔÇÏ¿© ºñ½ºÆ÷½ºÆ÷³×ÀÌÆ® Ä¡·á¸¦ ¹ÞÀº ȯÀÚ¿¡¼ ºñÁ¤Çü ÀüÀÚÇÏ ¹× °ñ°£ ´ëÅð°ñ °ñÀýÀÌ º¸°íµÈ ¹Ù ÀÖ´Ù. ¿ÜÀ̵µ °ñ±«»çÁõÀÌ ¸Å¿ì µå¹°°Ô º¸°íµÇ¾ú´Ù(ºñ½ºÆ÷½ºÆ÷³×ÀÌÆ® °è¿ ÀÌ»ó ¹ÝÀÀ). ¿ÜÀ̵µ °ñ±«»çÁõÀÌ ¸Å¿ì µå¹°°Ô º¸°íµÇ¾ú´Ù(ºñ½ºÆ÷½ºÆ÷³×ÀÌÆ® °è¿ ÀÌ»ó ¹ÝÀÀ).
13) ±¹³» ½ÃÆÇÈÄ Á¶»ç°á°ú(Á¶»çÁõ·Ê¼ö : 640¸í) ³ªÅ¸³ ÀÌ»ó¹ÝÀÀÀº ´ÙÀ½°ú °°À¸¸ç, ÀÌ ¾à°úÀÇ °ü·Ã ¿©ºÎ´Â È®½ÇÇÏÁö ¾Ê´Ù. : ¾ÈÅë, ±¸°¥
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 | ÇмúÁ¤º¸ |
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| 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]
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| Mechanism of Action |
Pamidronate¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ The mechanism of action of pamidronate is inhibition of bone resorption. Pamidronate adsorbs to calcium phosphate (hydroxyapatite) crystals in bone and may directly block dissolution of this mineral component of bone. In vitro studies also suggest that inhibition of osteoclast activity contributes to inhibition of bone resorption. Pamidronate also targets farnesyl pyrophosphate (FPP) synthase. Nitrogen-containing bisphosphonates (such as pamidronate, alendronate, risedronate, ibandronate and zoledronate) appear to act as analogues of isoprenoid diphosphate lipids, thereby inhibiting FPP synthase, an enzyme in the mevalonate pathway. Inhibition of this enzyme in osteoclasts prevents the biosynthesis of isoprenoid lipids (FPP and GGPP) that are essential for the post-translational farnesylation and geranylgeranylation of small GTPase signalling proteins. This activity inhibits osteoclast activity and reduces bone resorption and turnover. In postmenopausal women, it reduces the elevated rate of bone turnover, leading to, on average, a net gain in bone mass.
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| Pharmacology |
Pamidronate¿¡ ´ëÇÑ Pharmacology Á¤º¸ Pamidronate is in a class of drugs called bisphosphonates. Pamidronate reduces breakdown of the bones. Pamidronate is used in the treatment of Paget's disease of bone; to reduce high levels of calcium in the blood associated with malignancy (cancer); and to reduce the breakdown of bone due to metastases of breast cancer or multiple myeloma.
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| Metabolism |
Pamidronate¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Not Available
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| Protein Binding |
Pamidronate¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Approximately 54% (bound to human serum proteins)
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| Half-life |
Pamidronate¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ The mean ¡¾ SD elimination half-life is 28 ¡¾ 7 hours
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| Absorption |
Pamidronate¿¡ ´ëÇÑ Absorption Á¤º¸ Not Available
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| Pharmacokinetics |
Pamidronate DisodiumÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- ÀÛ¿ë¹ßÇö½Ã°£ : 24-48 ½Ã°£
- ÃÖ´ëÈ¿°ú ¹ßÇö½Ã°£ : 5-7ÀÏ
- ºÐÆ÷ : ºÐÆ÷¹Ý°¨±â : 1.6 ½Ã°£
- ´Ü¹é°áÇÕ :54 %
- ¹Ý°¨±â :
- ¼Ò½Ç : Á¤¸ÆÁÖÀÔÈÄ 72 ½Ã°£³»¿¡ Åõ¿©¿ë·®ÀÇ 20-55%°¡ ¹Ìº¯Èü·Î ´¢¿¡¼ ȸ¼öµÊ
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| Biotransformation |
Pamidronate¿¡ ´ëÇÑ Biotransformation Á¤º¸ Pamidronate is not metabolized and is exclusively eliminated by renal excretion
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| Toxicity |
Pamidronate¿¡ ´ëÇÑ Toxicity Á¤º¸ Side effects include an allergic reaction, kidney problems, seizures, low levels of calcium, magnesium, or phosphorus in the blood
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| Drug Interactions |
Pamidronate¿¡ ´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 |
Pamidronate¿¡ ´ëÇÑ Description Á¤º¸ Pamidronic acid (INN) or pamidronate disodium (USAN), marketed as pamidronate disodium pentahydrate under the brand name Aredia, is a bisphosphonate. [Wikipedia]
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| Dosage Form |
Pamidronate¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Powder, for solution IntravenousSolution Intravenous
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| Drug Category |
Pamidronate¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-inflammatory AgentsAntineoplastic AgentsBisphosphonatesBone Density Conservation Agents
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| Smiles String Canonical |
Pamidronate¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ NCCC(O)(P(O)(O)=O)P(O)(O)=O
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| Smiles String Isomeric |
Pamidronate¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ NCCC(O)(P(O)(O)=O)P(O)(O)=O
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| InChI Identifier |
Pamidronate¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C3H11NO7P2/c4-2-1-3(5,12(6,7)8)13(9,10)11/h5H,1-2,4H2,(H2,6,7,8)(H2,9,10,11)/f/h6-7,9-10H
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| Chemical IUPAC Name |
Pamidronate¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (3-amino-1-hydroxy-1-phosphonopropyl)phosphonic acid
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ÃÖ±ÙÁ¤º¸¼öÁ¤ÀÏ 2021-12-09
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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
Ã¥ÀÓÀ» ÁöÁö ¾Ê½À´Ï´Ù. ÀÚ¼¼ÇÑ ³»¿ëÀº ¡°Ã¥ÀÓÀÇ ÇÑ°è ¹× ¹ýÀû°íÁö¡±¸¦ ÂüÁ¶ÇØ ÁֽʽÿÀ.
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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