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1) ¼±Ãµ¼º QT°£°Ý¿¬Àå ȯÀÚ(ºÎÁ¤¸Æ, ½ÉÀüµµÀÌ»óÀ» ÀÏÀ¸Å³ ¼ö ÀÖ´Ù.)
2) ºÎÁ¤¸Æ ȯÀÚ
3) ³»Àμº ¿ì¿ïÁõ ȯÀÚ(Áõ»óÀÌ ¾Ç鵃 ¼ö ÀÖ´Ù.)
4) ÆÄŲ½¼ÁõÈıº ¶Ç´Â °£Áú ȯÀÚ(Áõ»óÀÌ ¾Ç鵃 ¼ö ÀÖ´Ù.)
5) ÁßÁõÀÇ ÁßÃ߽Űæ¾ïÁ¦ ¶Ç´Â È¥¼ö»óÅ ȯÀÚ
6) ÀÌ ¾à ¶Ç´Â µðÆä´ÒºÎÆ¿ÇÇÆä¸®µò À¯µµÃ¼¿¡ °ú¹ÎÁõÀÇ º´·ÂÀÌ Àִ ȯÀÚ
7) ¸¶Å©·Ñ¶óÀ̵å°è Ç×»ý¹°ÁúÀ» Åõ¿©¹Þ°í Àִ ȯÀÚ(ÀÌ ¾àÀÇ ´ë»ç¸¦ ÀúÇØÇÔ)
8) ÆÄ·Ï¼¼Æ¾ ¹× ´Ù¸¥ °·ÂÇÑ CYP2D6 ÀúÇØÁ¦ º´¿ëÅõ¿© ȯÀÚ(¡®6.»óÈ£Àۿ롯Ç× ÂüÁ¶)
9) HIV ´Ü¹éºÐÇØÈ¿¼Ò ÀúÇØÁ¦(ritonavir, ritonavir/ombitasvir/paritaprevir, saquinavir, indinavir, nelfinavir, atazanavir, fosamprenavir, darunavir), ¾ÆÁ¹°è Ç×Áø±ÕÁ¦(¿Ü¿ëÁ¦ Á¦¿Ü)(itraconazole, voriconazole, miconazole, fluconazole, fosfluconazole) ¹× cobicistat¸¦ Åõ¿©¹Þ°í Àִ ȯÀÚ(¡®6. »óÈ£Àۿ롯Ç× ÂüÁ¶)
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2) °£Àå¾Ö ȯÀÚ(°£Àå¾Ö°¡ ¾Ç鵃 ¼ö ÀÖ´Ù)
3) ½ÅÀå¾Ö ȯÀÚ(½ÉÀüµµÀÌ»óÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù)
4) ¿ïÇ÷¼º ½ÉºÎÀü µîÀÇ ½ÉÁúȯ ȯÀÚ(½ÉÀüµµÀÌ»óÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù)
5) QT°£°ÝÀ» ¿¬Àå½ÃŰ´Â ´Ù¸¥ ¾à¹°À» Åõ¿©ÁßÀΠȯÀÚ
6) Å©·Òģȼ¼Æ÷Á¾ ȯÀÚ
7) °©»ó¼±Áßµ¶Áõ ȯÀÚ
8) °£ÁúÀÇ ¼ÒÀÎ(¾ËÄڿñݴÜÁõ»ó, ³ú¼Õ»ó) ¶Ç´Â º´·ÂÀÌ Àִ ȯÀÚ, EEGÀÌ»ó ȯÀÚ(°æ·Ã¿ªÄ¡¸¦ ÀúÇϽÃų ¼ö ÀÖ´Ù.)
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1) ¼øÈ¯±â°è : ½ÉÀüµµÀÌ»ó(QT°£°ÝÀÇ ¿¬Àå, TÆÄÀÇ ÆòÀúÈ ¹× ¿ªÀü, À̺À¼º TÆÄ ¶Ç´Â UÆÄÀÇ ÃâÇö µî)¿¡ µû¸¥ µ¹¿¬»ç°¡ º¸°íµÇ¾î ÀÖÀ¸¹Ç·Î ƯÈ÷ QTºÎºÐ¿¡ º¯È°¡ ÀÖÀ¸¸é Åõ¿©¸¦ ÁßÁöÇÑ´Ù. ¶ÇÇÑ Ç÷Àü»öÀüÁõ(Æó»öÀüÁõ°ú ½ÉºÎÁ¤¸ÆÇ÷ÀüÁõ Æ÷ÇÔ, ºóµµºÒ¸í)ÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
2) ½Å°æÀÌ¿ÏÁ¦¾Ç¼ºÁõÈıº(Neuroleptic Malignant Syndrome) : ¿îµ¿¸¶ºñ, ½ÉÇÑ ±ÙÀ°°Á÷, ¿¬Çϰï¶õ, ºó¸Æ, Ç÷¾Ðº¯È, ¹ßÇÑ µîÀÌ ³ªÅ¸³ª°í ÀÌ·¯ÇÑ Áõ»ó°ú ÇÔ²² ¹ß¿ÀÌ ³ªÅ¸³ª´Â °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇϰí ü³Ã°¢°ú ¼öºÐº¸±Þ µîÀÇ Àü½ÅÀû Ä¡·á¿Í ÇÔ²² ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù. ÀÌ·¯ÇÑ Áõ»óÀÇ ¹ßÇö½Ã¿¡´Â ¹éÇ÷±¸Áõ°¡, Ç÷û CPK »ó½ÂÀÌ ÀÚÁÖ ³ªÅ¸³ª°í ¹Ì¿À±Û·Îºó´¢ÁõÀ» ¼ö¹ÝÇÑ ½Å±â´É ÀúÇϰ¡ ³ªÅ¸³¯ ¼ö ÀÖ´Ù. ¶ÇÇÑ À¯»çÈÇÕ¹°(ÇÒ·ÎÆä¸®µ¹ µî)¿¡¼ °í¿ÀÌ Áö¼ÓµÇ°í ÀǽÄÀå¾Ö, È£Èí°ï¶õ, ¼øÈ¯ÇãÅ»°ú Å»¼öÁõ»ó, ±Þ¼º½ÅºÎÀüÀ¸·Î ¹ßÀüÇØ¼ »ç¸ÁÇß´Ù´Â º¸°í°¡ ÀÖ´Ù.
3) Àú³ªÆ®·ýÇ÷Áõ : µå¹°°Ô ÀǽÄÀå¾Ö, °æ·Ã µîÀ» ¼ö¹ÝÇÏ´Â Àú³ªÆ®·ýÇ÷ÁõÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÀÌ·¯ÇÑ °æ¿ì¿¡´Â Áï½Ã Åõ¿©¸¦ ÁßÁöÇÏ°í ³ªÆ®·ýº¸Á¤ µîÀÇ ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù.
4) Ãßü¿Ü·ÎÁõ»ó : ÆÄŲ½¼ÁõÈıº(ÁøÀü, ±Ù°æÃà, À¯¿¬ µî), ¶§¶§·Î Á¤ÁºҴÉ(akathisia), ÀÌ»ó¿îµ¿Áõ[dyskinesia : ¾È±¸È¸Àü¹ßÀÛ, ¹ß¾î(Û¡åÞ)Àå¾Ö, ¿¬ÇÏÀå¾Ö µî]ÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÀÌ·¯ÇÑ °æ¿ì¿¡´Â °¨·® ¶Ç´Â ÇׯÄŲ½¼Á¦¿ÍÀÇ º´¿ëÅõ¿© µî ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù.
5) Á¤½Å½Å°æ°è : Á¹À½, ºÒ¸é, ºÒ¾È, ¶§¶§·Î ºÒ¿Â, ÈïºÐ, ÀÌ(ì¯)ÀÚ±ØÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù. ¶ÇÇÑ ¶§¶§·Î ȯ°¢, ¸Á»óÀÌ Çö¼ºÈµÉ ¼ö ÀÖ´Ù. ƯÈ÷ ÀÌÀü Ä¡·áÁ¦·ÎºÎÅÍ ÀÌ ¾àÀÇ Ä¡·á·Î ÀÌÇàÇÏ´Â °æ¿ì¿¡ ÀÌÀü Ä¡·áÁ¦ÀÇ Åõ¿©¸¦ °©ÀÚ±â ÁßÁöÇϰųª °¨·®Çϸé ÀÌ·¯ÇÑ Á¤½Å½Å°æ°è Áõ»óÀÌ ³ªÅ¸³ª±â ½¬¿ì¹Ç·Î ÀÌÀü Ä¡·áÁ¦¸¦ õõÈ÷ °¨·®ÇÏ´Â °ÍÀÌ ¹Ù¶÷Á÷ÇÏ´Ù. ¶ÇÇÑ ÀÌ·¯ÇÑ Áõ»óÀÌ ³ªÅ¸³ª´Â °æ¿ì¿¡´Â ÀÌ ¾àÀ» °¨·®Åõ¿©Çϰųª ÈÞ¾à ¹× ÀÌÀü Ä¡·áÁ¦¸¦ ¿ø·¡´ë·Î Åõ¿©ÇÏ´Â µî ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù. Ä¡·áÃʱ⿡ ÁÖÀǷ°¨¼Ò°¡ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¸ç ¾ËÄڿü·Ãë½Ã ÀÌ·¯ÇÑ Áõ»óÀÌ Áõ°µÉ ¼ö ÀÖ´Ù. Àú¿ë·®¿¡¼µµ °£Áú¼º ¹ßÀÛÀÌ º¸°íµÇ¾î ÀÖ´Ù.
6) °£Àå : µå¹°°Ô ALT, ASTÀÇ »ó½ÂÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
7) ´« : ¶§¶§·Î Á¶ÀýÀå¾Ö°¡ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
8) °ú¹ÎÁõ : ¶§¶§·Î ¹ßÁø, °¡·Á¿òÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÀÌ·¯ÇÑ °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇÑ´Ù.
9) ¼Òȱâ°è : ¶§¶§·Î ±¸¿ª, ±¸Åä, ½Ä¿åºÎÁø, À§ºÎºÒÄè°¨, º¯ºñ, º¹Åë, µå¹°°Ô ¼³»ç µîÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
10) ºñ´¢±â°è : ¶§¶§·Î ¹è´¢Àå¾Ö, µå¹°°Ô ºó´¢°¡ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
11) ±âŸ : ¶§¶§·Î ±¸°¥, ¹ßÇÑ, µÎÅë, ±Çۨ, ¼º¿åÇ×Áø, ºó¸Æ, ¾îÁö·¯¿ò, ºñƲ°Å¸², µå¹°°Ô ¾È¸éºÎÁ¾ÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
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1) ´Ù¸¥ Ç×Á¤½Åº´¾à°ú ¸¶Âù°¡Áö·Î ¾ËÄÚ¿Ã, ¼ö¸éÁ¦, ÁøÁ¤Á¦, °·ÂÇÑ ÁøÅëÁ¦ µî ÁßÃ߽Űæ¾ïÁ¦Á¦ÀÇ ÀÛ¿ëÀ» Áõ°½Ãų ¼ö ÀÖ´Ù.
2) ·¹º¸µµÆÄÀÇ ÇׯÄŲ½¼ÀÛ¿ëÀ» ÀúÇϽÃų ¼ö ÀÖ´Ù.
3) ÀÌ ¾àÀº °æ·Ã¿ªÄ¡¸¦ ÀúÇϽÃŰ¹Ç·Î Ç×°æ·ÃÁ¦¿Í º´¿ëÅõ¿©ÇÏ´Â °æ¿ì¿¡´Â Ç×°æ·ÃÁ¦¸¦ Áõ·®ÇÏ´Â µî ½ÅÁßÈ÷ Åõ¿©ÇÑ´Ù.
4) ÀÌ ¾àÀº QT°£°ÝÀ» ¿¬Àå½ÃŰ´Â °ÍÀ¸·Î º¸°íµÇ¾úÀ¸¹Ç·Î »ïȯ°è Ç׿ì¿ï¾à, Å׸£Æä³ªµò, ¾Æ½ºÅ×¹ÌÁ¹, ºÎÁ¤¸Æ¿ëÁ¦, Æä³ëÄ¡¾ÆÁø°è ¾à¹°, Äû´Ñ, ¸ÞÇ÷ÎÄý µî QT¿¬ÀåÀ» ÀÏÀ¸Å²´Ù°í ¾Ë·ÁÁø ¾à¹°°ú º´¿ëÅõ¿©ÇÏÁö ¾Ê´Â´Ù.
5) ÀÌ´¢Á¦ µî ÀüÇØÁú ºÒ±ÕÇüÀ» À¯¹ßÇÏ´Â ¾à¹°Àº ÀúÄ®·ýÇ÷ÁõÀÇ À§ÇèÀÌ ÀÖÀ¸¹Ç·Î º´¿ëÅõ¿©ÇÏÁö ¾Ê´Â °ÍÀÌ ¹Ù¶÷Á÷ÇÏ´Ù(Ä®·ýº¸Á¸¼º ÀÌ´¢Á¦¸¦ »ç¿ëÇÑ´Ù).
6) CYP2D6 ÀúÇØÁ¦ : ´Üȸ Àú¿ë·® ÇǸðÁöµå(2mg)¸¦ ÆÄ·Ï¼¼Æ¾°ú º´¿ëÅõ¿©ÇÑ ¿¬±¸¿¡¼ ÇǸðÁöµåÀÇ ³óµµ Áõ°¡°¡ °üÂûµÇ¾ú´Ù. ÀÌ·¯ÇÑ Áõ°¡´Â ÆÄ·Ï¼¼Æ¾ÀÇ CYP2D6 ÀúÇØ È¿°ú¿Í ¿¬°üÀÌ ÀÖ´Ù. ÇǸðÁöµå¿Í ÆÄ·Ï¼¼Æ¾ ¶Ç´Â ´Ù¸¥ °·ÂÇÑ CYP2D6 ÀúÇØÁ¦¿Í º´¿ëÅõ¿©´Â ±Ý±âÀÌ´Ù.
7) ÀÌ ¾à°ú HIV ´Ü¹éºÐÇØÈ¿¼Ò ÀúÇØÁ¦(ritonavir, ritonavir/ombitasvir/paritaprevir, saquinavir, indinavir, nelfinavir, atazanavir, fosamprenavir, darunavir), ¾ÆÁ¹°è Ç×Áø±ÕÁ¦(¿Ü¿ëÁ¦ Á¦¿Ü)(itraconazole, voriconazole, miconazole, fluconazole, fosfluconazole) ¹× cobicistat º´¿ëÅõ¿©½Ã CYP3A4 ¾ïÁ¦·Î ÀÎÇÏ¿© ÇǸðÁþÀÇ Ç÷Áß³óµµ Áõ°¡´Â QT¿¬Àå ¹× ½É½Ç¼ººÎÁ¤¸ÆÀ» À¯¹ßÇÒ ¼ö ÀÖÀ¸¹Ç·Î º´¿ëÅõ¿©´Â ±Ý±âÀÌ´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 |
³»¿ë |
| DUR (ÀǾàǰ»ç¿ëÆò°¡) |
º´¿ë±Ý±â :
[amantadine sulfate]
[amiodarone hydrochloride]
[amitriptyline hydrochloride]
[atazanavir sulfate (as atazanavir)+cobicistat silicon dioxide (as cobicistat)]
[clarithromycin]
[clarithromycin]
[cobicistat silicon dioxide (as cobicistat )+darunavir ethanolate (as darunavir)]
[cobicistat silicon dioxide (as cobicistat)+elvitegravir+emtricitabine+tenofovir alafenamide fumarate (as tenofovir alafenamide)]
[darunavir ethanolate (as darunavir)]
[domperidone]
[domperidone maleate (as domperidone)]
[dronedarone]
[dronedarone]
[escitalopram oxalate (as escitalopram)]
[escitalopram oxalate (as escitalopram)]
[fluconazole]
[fluconazole]
[fluoxetine hydrochloride (as fluoxetine)]
[fluoxetine hydrochloride (as fluoxetine)]
[fosaprepitant dimeglumine (as fosaprepitant)]
[haloperidol]
[haloperidol decanoate (as haloperidol)]
[haloperidol decanoate (as haloperidol)]
[imipramine hydrochloride]
[itraconazole]
[itraconazole]
[letermovir]
[lorlatinib]
[mizolastine]
[nirmatrelvir+ritonavir]
[nortriptyline hydrochloride (as nortriptyline)]
[paroxetine hydrochloride (as paroxetine)]
[paroxetine hydrochloride (as paroxetine)]
[posaconazole(micronized)]
[ritonavir]
[roxithromycin]
[roxithromycin]
[sertraline hydrochloride (as sertraline)]
[sertraline hydrochloride (as sertraline)]
[voriconazole]
[ziprasidone hydrochloride monohydrate (as ziprasidone)]
[»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 |
Pimozide¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ The ability of pimozide to suppress motor and phonic tics in Tourette's Disorder is thought to be primarily a function of its dopaminergic blocking activity. Pimozide binds to the dopamine D2 receptor in the CNS. It also appears to block voltage-operated calcium channels and acts as an antagonist at opiate receptors (OP2).
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| Pharmacology |
Pimozide¿¡ ´ëÇÑ Pharmacology Á¤º¸ Pimozide is an orally active antipsychotic drug product which shares with other antipsychotics the ability to blockade dopaminergic receptors on neurons in the central nervous system. However, receptor blockade is often accompanied by a series of secondary alterations in central dopamine metabolism and function which may contribute to both pimozide's therapeutic and untoward effects. In addition, pimozide, in common with other antipsychotic drugs, has various effects on other central nervous system receptor systems which are not fully characterized. Pimozide also has less potential for inducing sedation and hypotension as it has more specific dopamine receptor blocking activity than other neuroleptic agents (and is therefore a suitable alternative to haloperidol).
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| Metabolism |
Pimozide¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 3A4 (CYP3A4)Cytochrome P450 1A2 (CYP1A2)Aromatic-L-amino-acid decarboxylase (AADC)
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| Protein Binding |
Pimozide¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Not Available
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| Half-life |
Pimozide¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 29 ¡¾ 10 hours (single-dose study of healthy volunteers).
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| Absorption |
Pimozide¿¡ ´ëÇÑ Absorption Á¤º¸ Greater than 50% absorption after oral administration. Serum peak appears 6-8 hours post ingestion.
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| Pharmacokinetics |
PimozideÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- Èí¼ö : °æ±¸ : 50%
- ´Ü¹é°áÇÕ : 99%
- ´ë»ç : °£´ë»ç, À¯ÀÇÇÑ ÃÊȸÅë°úÈ¿°ú
- ¹Ý°¨±â : 50½Ã°£
- Ç÷ÁßÃÖ°í³óµµ µµ´Þ½Ã°£ : 6-8 ½Ã°£ À̳»
- ¼Ò½Ç : ½Å¹è¼³
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| Biotransformation |
Pimozide¿¡ ´ëÇÑ Biotransformation Á¤º¸ Notable first-pass metabolism in the liver, primarily by N-dealkylation via the cytochrome P450 isoenzymes CYP3A and CYP1A2 (and possibly CYP2D6). The activity of the two major metabolites has not been determined.
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| Toxicity |
Pimozide¿¡ ´ëÇÑ Toxicity Á¤º¸ LD50 = 1100 mg/kg (rat, oral), 228 mg/kg (mouse, oral)
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| Drug Interactions |
Pimozide¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Amprenavir Amprenavir increases the effect and toxicity of pimozideFosamprenavir Amprenavir increases the effect and toxicity of pimozideImatinib Imatinib increases the effect and toxicity of pimozideNefazodone increases the effect and toxicity of pimozideNelfinavir Nelfinavir increases the effect and toxicity of pimozideSaquinavir The protease inhibitor increases the effect and toxicity of pimozideRitonavir The protease inhibitor increases the effect and toxicity of pimozideIndinavir The protease inhibitor increases the effect and toxicity of pimozideAtazanavir The protease inhibitor increases the effect and toxicity of pimozideCitalopram The SSRI increases the effect and toxicity of pimozideEscitalopram The SSRI increases the effect and toxicity of pimozideSertraline The SSRI increases the effect and toxicity of pimozideZiprasidone Increased risk of cardiotoxicity and arrhythmiasZileuton Increased risk of cardiotoxicity and arrhythmiasVoriconazole Increased risk of cardiotoxicity and arrhythmiasTroleandomycin Increased risk of cardiotoxicity and arrhythmiasThioridazine Increased risk of cardiotoxicity and arrhythmiasTelithromycin Increased risk of cardiotoxicity and arrhythmiasPosaconazole Contraindicated co-administrationParoxetine Increased risk of cardiotoxicity/arrhythmiasMesoridazine Increased risk of cardiotoxicity and arrhythmiasKetoconazole Increased risk of cardiotoxicity and arrhythmiasJosamycin Increased risk of cardiotoxicity and arrhythmiasItraconazole Increased risk of cardiotoxicity and arrhythmiasFluconazole Increased risk of cardiotoxicity and arrhythmiasErythromycin Increased risk of cardiotoxicity and arrhythmiasClarithromycin Increased risk of cardiotoxicity and arrhythmiasAprepitant Increased risk of cardiotoxicity and arrhythmiasDonepezil Possible antagonism of actionGalantamine Possible antagonism of actionRivastigmine Possible antagonism of action
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸] Pimozide¿¡ ´ëÇÑ P450 table
SUBSTRATES
CYP 3A4/3A5/3A7
Macrolide antibiotics:
clarithromycin
erythromycin
NOT azithromycin
telithromycin
Anti-arrhythmics:
quinidine
Benzodiazepines:
alprazolam
diazepam
midazolam
triazolam
Immune Modulators:
cyclosporine
tacrolimus (FK506)
HIV Protease Inhibitors:
indinavir
ritonavir
saquinavir
Prokinetic:
cisapride
Antihistamines:
astemizole
chlorpheniramine
Calcium Channel Blockers:
amlodipine
diltiazem
felodipine
nifedipine
nisoldipine
nitrendipine
verapamil
HMG CoA Reductase Inhibitors:
atorvastatin
cerivastatin
lovastatin
NOT pravastatin
simvastatin
aripiprazole
buspirone
gleevec
haloperidol (in part)
methadone
**pimozide**
quinine
NOT rosuvastatin
sildenafil
tamoxifen
trazodone
vincristine
INHIBITORS
CYP 3A4/3A5/3A7
HIV Protease Inhibitors:
indinavir
nelfinavir
ritonavir
amiodarone
NOT azithromycin
cimetidine
clarithromycin
diltiazem
erythromycin
fluvoxamine
grapefruit juice
itraconazole
ketoconazole
mibefradil
nefazodone
troleandomycin
verapamil
INDUCERS
CYP 3A4/3A5/3A7
carbamazepine
phenobarbital
phenytoin
rifabutin
rifampin
St. John's wort
troglitazone
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| Food Interaction |
Pimozide¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take without regard to meals.Grapefruit and grapefruit juice should be avoided throughout treatment. Grapefruit can increase serum levels of this product.
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| Drug Target |
[Drug Target]
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| Description |
Pimozide¿¡ ´ëÇÑ Description Á¤º¸ A diphenylbutylpiperidine that is effective as an antipsychotic agent and as an alternative to haloperidol for the suppression of vocal and motor tics in patients with Tourette syndrome. Although the precise mechanism of action is unknown, blockade of postsynaptic dopamine receptors has been postulated. (From AMA Drug Evaluations Annual, 1994, p403)
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| Dosage Form |
Pimozide¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Tablet Oral
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| Drug Category |
Pimozide¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Dyskinesia AgentsAntipsychotic AgentsDopamine Antagonists
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| Smiles String Canonical |
Pimozide¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ FC1=CC=C(C=C1)C(CCCN1CCC(CC1)N1C(=O)NC2=CC=CC=C12)C1=CC=C(F)C=C1
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| Smiles String Isomeric |
Pimozide¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ FC1=CC=C(C=C1)C(CCCN1CCC(CC1)N1C(=O)NC2=CC=CC=C12)C1=CC=C(F)C=C1
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| InChI Identifier |
Pimozide¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C28H29F2N3O/c29-22-11-7-20(8-12-22)25(21-9-13-23(30)14-10-21)4-3-17-32-18-15-24(16-19-32)33-27-6-2-1-5-26(27)31-28(33)34/h1-2,5-14,24-25H,3-4,15-19H2,(H,31,34)/f/h31H
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| Chemical IUPAC Name |
Pimozide¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 3-[1-[4,4-bis(4-fluorophenyl)butyl]piperidin-4-yl]-1H-benzimidazol-2-one
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| Drug-Induced Toxicity Related Proteins |
PIMOZIDE ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸ Replated Protein:G protein-activated inward rectifier potassium channel Drug:pimozide Toxicity:sinus tachycardia. [¹Ù·Î°¡±â] Replated Protein:G protein-activated inward rectifier potassium channel Drug:pimozide Toxicity:sinus tachycardia. [¹Ù·Î°¡±â] Replated Protein:G protein-activated inward rectifier potassium channel Drug:pimozide Toxicity:seizures. [¹Ù·Î°¡±â] Replated Protein:G protein-activated inward rectifier potassium channel Drug:pimozide Toxicity:seizures. [¹Ù·Î°¡±â]
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ÃÖ±ÙÁ¤º¸¼öÁ¤ÀÏ 2023-03-31
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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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»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. |
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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.
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
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