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ÄÄÇÁ·ÎÁ¾à [Prochlorperazine]
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Àü¹®ÀǾàǰ | »èÁ¦
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µå·°ÀÎÆ÷¿¡¼´Â ÀǾàǰ ÀÎÅÍ³Ý ÆÇ¸Å¸¦ ÇÏÁö ¾Ê½À´Ï´Ù. |
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À¯·áȸ¿ø °áÀç½Ã¿¡´Â º¸´Ù ´Ù¾çÇÑ ¾à¹°Á¤º¸¸¦
ÀÌ¿ëÇÏ½Ç ¼ö ÀÖ½À´Ï´Ù.
À¯·áÁ¤º¸¸ñ·ÏÀº Àü¹®È¸¿øÀ¸·Î
·Î±×ÀÎ ÇϽøé È®ÀÎ °¡´ÉÇÕ´Ï´Ù.
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| Ç׸ñ |
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û±¸ÄÚµå(KDÄÚµå) ºñ±Þ¿©Á¡°ËÄÚµå »óÇÑ±Ý¾× |
[E10150031]
[º¸ÇèÄڵ忡 µû¸¥ ¾àǰ±âº»Á¤º¸ Á÷Á¢Á¶È¸]
\0 ¿ø/1°³(2007.03.01)(ÇöÀç¾à°¡)
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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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1ÀÏ 2ȸ, 1ȸ 1°³¸¦ Á÷Àå³» »ðÀÔ
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ÀÌ ¾à¿¡ ÀÇÇØ 2Â÷ÀûÀ¸·Î ¹ß»ýÇÒ ¼ö ÀÖ´Â Ãßü¿Ü·Î Áõ»óÀº ±¸Åä, Rey's syndrome ¶Ç´Â ±âŸ ³úÁúȯ¿¡ ±âÀÎÇÑ, Áø´ÜµÇÁö ¾ÊÀº 1Â÷ÁúȯÀÇ ÁßÃ߽Űæ°è Áõ»ó°ú È¥µ¿µÉ ¼ö ÀÖ´Ù.
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1) È¥¼ö»óÅÂÀ̰ųª ¾ËÄÚ¿Ã, ¹Ù¸£ºñÆ®·¹ÀÌÆ®·ù, ¸¶¾à·ù µî ÁßÃ߽Űæ¾ïÁ¦Á¦¸¦ ´Ù·® º¹¿ëÇÑ »óÅÂÀÇ È¯ÀÚ
2) ¼Ò¾Æ ¼ö¼ú ȯÀÚ
3) 2¼¼ ÀÌÇÏ ¶Ç´Â 20lbs(ÆÄ¿îµå) ÀÌÇÏ ¼Ò¾Æ
4) Rey's syndrome ȯÀÚ
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1) Á¹¸², ¾îÁö·¯¿ò, ¹«¿ù°æ, ´«ÀÌ Èå·ÁÁü, ÇǺιÝÀÀ ¹× ÀúÇ÷¾ÐÀÌ ÀϾ ¼ö ÀÖÀ¸¸ç, ¸¸ÀÏ °¨±â¿Í °°Àº Áõ»ó°ú ´õºÒ¾î ¹ß¿À» º¸À̸é ÀûÀýÇÑ °£°Ë»ç¸¦ ½Ç½ÃÇÏ¿©¾ß Çϰí, °Ë»ç°á°ú ºñÁ¤»óÀ̸é, Ä¡·á¸¦ Áß´ÜÇÒ °Í.
2) ¹éÇ÷±¸ °¨¼ÒÁõ°ú ¹«°ú¸³±¸ÁõÀÌ µå¹°°Ô º¸°íµÈ ¹Ù ÀÖÀ¸¸ç, ÀÌ·¯ÇÑ °æ¿ì Ä¡·á¸¦ Áß´ÜÇϰí ÀÇ»ç¿Í »óÀÇÇÒ °Í.
3) Ãßü¿Ü·Î ¹ÝÀÀÀÌ ÀϾ ¼ö ÀÖÀ¸¸ç Áõ»óÀÇ °æÁß¿¡ µû¶ó ¿ë·®À» ÁÙÀ̰ųª Åõ¾àÀ» Áß´ÜÇØ¾ß ÇÔ.
¨ç ¿îµ¿ºÒ¾È : °Ý¾Ó ȤÀº ¾ÈÀýºÎÀý°ú ¶§¶§·Î ºÒ¸éÁõÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ½.
¨è ±ÙÀ°±äÀå : ¸ñ±ÙÀ°ÀÇ °æ·Ã, µî±ÙÀ°ÀÇ ½Å±Ù°æÃà, ¼Õ¹ß±ÙÀ°ÀÇ °æ·Ã, ¾ß°£±äÀå, ¿¬Çϰï¶õ, µ¿¾ÈÇѰèÀ§Çè, ÇôÀÇ µ¹Ãâ µîÀÌ µå¹°°Ô ³ªÅ¸³¯ ¼ö ÀÖÀ½.
¨é À§-ÆÄŲ½¼º´ : À¯¿¬; ÁøÀüȯÁ¦ Á¦Á¶¾ç ¿îµ¿; Â÷°ñ°æÁ÷; ¹ßÀ» ÁúÁú²ø¸ç °È´Â º¸ÇàÀÌ µå¹°°Ô ³ªÅ¸³².
¨ê ¸¸¹ß¼º ¿îµ¿Àå¾Ö : Àå±âÄ¡·á ȯÀÚ¿¡ ³ªÅ¸³¯ ¼ö ÀÖÀ½.
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1) º» Á¦ÀÇ ÁøÅäÀÛ¿ë¿¡ ÀÇÇØ ´Ù¸¥ ¾à¹°ÀÇ °ú·®À¸·Î ÀÎÇÑ ±¸Åä/±¸¿ªÀ» ÀºÆóÇϰųª Àå Æó¼â¡¤³úÁ¾¾ç µîÀÇ Áø´ÜÀ» È帮°Ô ÇÒ ¼ö ÀÖ´Ù.
2) Ç×¾ÏÁ¦¿Í º´¿ë ½Ã ÀÌµé ¾à¹°ÀÇ µ¶¼ºÀ¸·Î ÀÎÇÑ ±¸Åä°¡ »ç¶óÁú ¼ö ÀÖ´Ù.
3) ÀúÇ÷¾Ð°ú ½É¸Æ°ü¼º Àå¾Ö ȯÀÚ¿¡°Ô °í¿ë·® Åõ¿© ½Ã ÁÖÀǰ¡ ¿ä¸ÁµÈ´Ù.
4) °ú¿ë·®À¸·Î ±íÀº Àá°ú È¥ÂÚ°¡ º¸°íµÈ ¹Ù ÀÖ´Ù.
5) µå¹°°Ô ÇÁ·Ñ¶ôƾ ¼öÄ¡ÀÇ »ó½ÂÀÌ °ËÃâµÈ °æ¿ì°¡ ½Å°æÀÌ¿ÏÁ¦¿¡¼ °øÅëÀûÀ¸·Î ³ªÅ¸³ªÁö¸¸ ÀÓ»óÀûÀ¸·Î ÁÖ¸ñÇÒ ¸¸ÇÑ »ó½ÂÀº º¸°íµÈ ¹Ù ¾ø´Ù.
6) ³ì³»Àå ȯÀÚ¿¡ »ç¿ë ½Ã ÁÖÀǰ¡ ¿ä¸ÁµÈ´Ù.
7) Æä³ëÄ¡¾ÆÁø°è ¾à¹°µéÀº ü¿ÂÁ¶Àý±âÀüÀ» ¹æÇØÇÒ ¼ö Àֱ⠶§¹®¿¡ ¸Å¿ì ¶ß°Å¿î ȯ°æÀ̳ª ¹°Áú¿¡ ³ëÃâµÇ´Â °Í¿¡ ´ëÇØ ÁÖÀǰ¡ ¿ä¸ÁµÈ´Ù.
8) Æä³ëÄ¡¾ÆÁø°è ¾à¹°µéÀº °æ±¸¿ë Ç×ÀÀ°íÁ¦ÀÇ È¿°ú¸¦ °æ°¨½Ãų ¼ö ÀÖÀ¸¸ç ¾ËÆÄ-¾Æµå·¹³¯¸°¼º Â÷´ÜÀÛ¿ëÀ» ÀÏÀ¸Å³ ¼ö ÀÖ´Ù.
9) Æä³ëÄ¡¾ÆÁø°è ¾à¹°°ú ÇÁ·ÎÇÁ¶ó³ë·ÑÀ» º´¿ëÇÏ¸é µÎ ¾à¹° ¸ðµÎ Ç÷Àå¼öÄ¡°¡ »ó½ÂÇϸç Ç×Àü°£Á¦¿Í º´¿ë½Ã Àü°£¿ªÄ¡¸¦ ÀúÇϽÃų ¼ö ÀÖÀ¸¹Ç·Î Ç×Àü°£Á¦ÀÇ ¿ë·®À» Á¶ÀýÇÒ Çʿ䰡 ÀÖÀ» ¼ö ÀÖ´Ù.
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| Mechanism of Action |
Prochlorperazine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Prochlorperazine blocks the D2 somatodendritic autoreceptor, resulting in the blockade of postsynaptic dopamine receptors in the mesolimbic system and an increased dopamine turnover. The antiemetic effects of prochlorperazine can be attributed to dopamine blockade in the chemoreceptor trigger zone. Prochlorperazine also blocks anticholinergic and alpha-adrenergic receptors, the blockade of alpha(1)-adrenergic receptors resulting in sedation, muscle relaxation, and hypotension.
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| Pharmacology |
Prochlorperazine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Prochlorperazine is a piperazine phenothiazine related to high-potency neuroleptics such as perphenazine. It shares many of the actions and adverse effects of the antipsychotics.
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| Protein Binding |
Prochlorperazine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 91-99%
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| Half-life |
Prochlorperazine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 6 to 8 hours
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| Absorption |
Prochlorperazine¿¡ ´ëÇÑ Absorption Á¤º¸ Rapidly absorbed following oral administration
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| Pharmacokinetics |
ProchlorperazineÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- ÀÛ¿ë¹ßÇö½Ã°£ :
- °æ±¸ : 30-40ºÐ À̳»
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- ÀÛ¿ëÁö¼Ó½Ã°£ :
- ±ÙÀ°ÁÖ»ç, °æ±¸¿ë ¼¹æÇü Á¦Á¦ : 12½Ã°£
- °æ±¸¿ë ¼Ó¹æÇü Á¦Á¦, Á÷Àå³» Åõ¿© : 3-4 ½Ã°£
- ºÐÆ÷ : ÅÂ¹Ý Åë°ú, À¯Áó ºÐºñ
- ´ë»ç : °£´ë»ç
- ¹Ý°¨±â : 23½Ã°£
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| Biotransformation |
Prochlorperazine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic. Undergoes metabolism in the gastric mucosa and on first pass through the liver, CYP2D6 and/or CYP3A4.
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| Toxicity |
Prochlorperazine¿¡ ´ëÇÑ Toxicity Á¤º¸ Symptoms of central nervous system depression to the point of somnolence or coma. Agitation and restlessness may also occur. Other possible manifestations include convulsions, EKG changes and cardiac arrhythmias, fever and autonomic reactions such as hypotension, dry mouth and ileus; LD50=400mg/kg (orally in mice)
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| Drug Interactions |
Prochlorperazine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Amphetamine Decreased anorexic effect, may increase pyschotic symptomsBenzphetamine Decreased anorexic effect, may increase pyschotic symptomsBromocriptine The phenothiazine decreases the effect of bromocriptineDextroamphetamine Decreased anorexic effect, may increase pyschotic symptomsDexfenfluramine Decreased anorexic effect, may increase pyschotic symptomsDiethylpropion Decreased anorexic effect, may increase pyschotic symptomsFenfluramine Decreased anorexic effect, may increase pyschotic symptomsMazindol Decreased anorexic effect, may increase pyschotic symptomsMethamphetamine Decreased anorexic effect, may increase pyschotic symptomsMetrizamide Increased risk of convulsionsGuanethidine The agent decreases the effect of guanethidinePhendimetrazine Decreased anorexic effect, may increase pyschotic symptomsPhenmetrazine Decreased anorexic effect, may increase pyschotic symptomsPhentermine Decreased anorexic effect, may increase pyschotic symptomsPhenylpropanolamine Decreased anorexic effect, may increase pyschotic symptomsRivastigmine Possible antagonism of actionGalantamine Possible antagonism of actionDonepezil Possible antagonism of actionCisapride Increased risk of cardiotoxicity and arrhythmiasGatifloxacin Increased risk of cardiotoxicity and arrhythmiasGrepafloxacin Increased risk of cardiotoxicity and arrhythmiasLevofloxacin Increased risk of cardiotoxicity and arrhythmiasSparfloxacin Increased risk of cardiotoxicity and arrhythmiasTerfenadine Increased risk of cardiotoxicity and arrhythmias
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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 |
Prochlorperazine¿¡ ´ëÇÑ Description Á¤º¸ A phenothiazine antipsychotic used principally in the treatment of nausea; vomiting; and vertigo. It is more likely than chlorpromazine to cause extrapyramidal disorders. (From Martindale, The Extra Pharmacopoeia, 30th ed, p612)
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| Dosage Form |
Prochlorperazine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Liquid IntravenousSolution IntravenousSuppository RectalTablet Oral
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| Drug Category |
Prochlorperazine¿¡ ´ëÇÑ Drug_Category Á¤º¸ AntiemeticsAntipsychotic AgentsAntipsychoticsDopamine AntagonistsPhenothiazines
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| Smiles String Canonical |
Prochlorperazine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CN1CCN(CCCN2C3=CC=CC=C3SC3=C2C=C(Cl)C=C3)CC1
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| Smiles String Isomeric |
Prochlorperazine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CN1CCN(CCCN2C3=CC=CC=C3SC3=C2C=C(Cl)C=C3)CC1
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| InChI Identifier |
Prochlorperazine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C20H24ClN3S/c1-22-11-13-23(14-12-22)9-4-10-24-17-5-2-3-6-19(17)25-20-8-7-16(21)15-18(20)24/h2-3,5-8,15H,4,9-14H2,1H3
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| Chemical IUPAC Name |
Prochlorperazine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 2-chloro-10-[3-(4-methylpiperazin-1-yl)propyl]phenothiazine
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| Drug-Induced Toxicity Related Proteins |
PROCHLORPERAZINE ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸ Replated Protein:UDP-glucuronosyltransferase Drug:prochlorperazine Toxicity:disruption of the structural organization. [¹Ù·Î°¡±â] Replated Protein:Glucose-6-phosphatase Drug:prochlorperazine Toxicity:disruption of the structural organization. [¹Ù·Î°¡±â]
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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.
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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