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| Mechanism of Action |
Cholestyramine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Cholestyramine binds bile in the gastrointestinal tract to prevent its reabsorption. The resin is a strong anion exchange resin, which means that it can exchange its chloride anions with anionic bile acids in the gastrointestinal tract and bind them strongly in the resin matrix. The functional group of the anion exchange resin is a quaternary ammonium group attached to an inert styrene-divinylbenzene copolymer.
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| Pharmacology |
Cholestyramine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Cholesterol is probably the sole precursor of bile acids. During normal digestion, bile acids are secreted into the intestines. A major portion of the bile acids is absorbed from the intestinal tract and returned to the liver via the enterohepatic circulation. Only very small amounts of bile acids are found in normal serum. Cholestyramine resin adsorbs and combines with the bile acids in the intestine to form an insoluble complex which is excreted in the feces. This results in a partial removal of bile acids from the enterohepatic circulation by preventing their absorption.
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| Metabolism |
Cholestyramine¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Liver carboxylesterase
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| Half-life |
Cholestyramine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 6 minutes
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| Absorption |
Cholestyramine¿¡ ´ëÇÑ Absorption Á¤º¸ Not absorbed from the gastrointestinal tract following oral administration.
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| Pharmacokinetics |
Cholestyramine ResinÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- ÃÖ´ëÈ¿°ú ¹ßÇö½Ã°£ : 21ÀÏ
- Èí¼ö : À§Àå°ü¿¡¼ Èí¼ö ¾ÈµÊ
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| Biotransformation |
Cholestyramine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Bile acids
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| Toxicity |
Cholestyramine¿¡ ´ëÇÑ Toxicity Á¤º¸ Overdose may result in blockage of intestine or stomach.
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| Drug Interactions |
Cholestyramine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Methotrexate Decreased levels of methotrexateAnisindione The gastro-intestinal binding agent decreases the anticoagulant effectDicumarol The gastro-intestinal binding agent decreases the anticoagulant effectAcenocoumarol The gastro-intestinal binding agent decreases the anticoagulant effectWarfarin The gastro-intestinal binding agent decreases the anticoagulant effectDigoxin The resin decreases the effect of digoxinEzetimibe Decreases the levels of ezetimibeFluvastatin Increased/decreased effect according to spacingHydrocortisone Decreases the effect of hydrocortisoneLevothyroxine The resin decreases the absorption of thyroid hormonesLiothyronine The resin decreases the absorption of thyroid hormonesRaloxifene The resin decreases the effect of raloxifeneSpironolactone Increased risk of acidosis and hyperkaliemiaTroglitazone Decreases the effect of troglitazoneLiotrix The resin decreases the absorption of thyroid hormonesThyroglobulin The resin decreases the absorption of thyroid hormonesUrsodeoxycholic acid The resin decreases the effect of ursodiolAcenocoumarol The gastro-intestinal binding agent decreases the anticoagulant effect
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Cholestyramine¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take with food, do not mix with soft drinks.
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| Description |
Cholestyramine¿¡ ´ëÇÑ Description Á¤º¸ Cholestyramine or colestyramine is a bile acid sequestrant. Bile acid sequestrants are polymeric compounds which serve as ion exchange resins. Cholestyramine resin is quite hydrophilic, but insoluble in water.
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| Dosage Form |
Cholestyramine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Powder OralPowder, for solution OralPowder, for suspension Oral
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| Drug Category |
Cholestyramine¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anticholesteremic AgentsAntihyperlipidemicsCholesterol Absorption Inhibitors
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| Smiles String Canonical |
Cholestyramine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ Not Available
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| Smiles String Isomeric |
Cholestyramine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ Not Available
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| InChI Identifier |
Cholestyramine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ Not Available
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| Chemical IUPAC Name |
Cholestyramine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ Not Available
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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
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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