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| 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]
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| µ¶¼ºÁ¤º¸ |
Lorazepam¿¡ ´ëÇÑ µ¶¼ºÁ¤º¸ : Á¤º¸º¸±â
Ãâó: ±¹¸³µ¶¼º°úÇпø µ¶¼º¹°ÁúÁ¤º¸DB : http://www.nitr.go.kr/nitr/contents/m134200/view.do |
| Mechanism of Action |
Lorazepam¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Lorazepam binds to central benzodiazepine receptors which interact allosterically with GABA receptors. This potentiates the effects of the inhibitory neurotransmitter GABA, increasing the inhibition of the ascending reticular activating system and blocking the cortical and limbic arousal that occurs following stimulation of the reticular pathways.
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| Pharmacology |
Lorazepam¿¡ ´ëÇÑ Pharmacology Á¤º¸ Lorazepam, a benzodiazepine not transformed to active metabolites, is used to treat anxiety, status epilepticus, and for sedation induction and anterograde amnesia.
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| Metabolism |
Lorazepam¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:UDP-glucuronic acidMonoamine oxidase type A (MAO-A)
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| Protein Binding |
Lorazepam¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 85%
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| Half-life |
Lorazepam¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 12 hours
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| Absorption |
Lorazepam¿¡ ´ëÇÑ Absorption Á¤º¸ Readily absorbed with an absolute bioavailability of 90%.
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| Pharmacokinetics |
LorazepamÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- ¼ö¸éÀÛ¿ë ¹ßÇö½Ã°£ : ±ÙÀ°ÁÖ»ç : 20-30ºÐ
- ÀÛ¿ëÁö¼Ó½Ã°£ : 6-8 ½Ã°£
- Èí¼ö : °æ±¸, ±ÙÀ°ÁÖ»ç : ½Å¼ÓÈ÷ Èí¼öµÊ
- ºÐÆ÷ : ºÐÆ÷¿ëÀû :
- ½Å»ý¾Æ : 0.76 L/kg
- ¼ºÀÎ : 1.3 L/kg
- ´Ü¹é°áÇÕ : 85%. ³ëÀΠȯÀÚ¿¡¼´Â ºñ°áÇÕ ºÐÀ²ÀÌ ³ô¾ÆÁø´Ù.
- ´ë»ç : °£¿¡¼ ºñȰ¼ºÃ¼·Î ´ë»çµÈ´Ù.
- ¹Ý°¨±â :
- ½Å»ý¾Æ : 40.2 ½Ã°£
- ¼Ò¾Æ : 10.5 ½Ã°£
- ¼ºÀÎ : 12.9 ½Ã°£
- ³ëÀÎ : 15.9 ½Ã°£
- ¸»±â ½ÅÁúȯ : 32-70 ½Ã°£
- ¼Ò½Ç : ½Å¹è¼³µÇ¸ç, ´ëº¯À¸·Î ¹è¼³µÇ´Â ¾çÀº ¸Å¿ì Àû´Ù.
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| Biotransformation |
Lorazepam¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic
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| Toxicity |
Lorazepam¿¡ ´ëÇÑ Toxicity Á¤º¸ Somnolence, confusion, and coma, LD50=3178mg/kg (orally in mice).
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| Drug Interactions |
Lorazepam¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Clozapine Increased risk of toxicityEthotoin Possible increased levels of the hydantoin, decrease of benzodiazepineFosphenytoin Possible increased levels of the hydantoin, decrease of benzodiazepineMephenytoin Possible increased levels of the hydantoin, decrease of benzodiazepinePhenytoin Possible increased levels of the hydantoin, decrease of benzodiazepineKava Kava increases the effect of the benzodiazepine
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Lorazepam¿¡ ´ëÇÑ Food Interaction Á¤º¸ Avoid alcohol.Take with food.Avoid excessive quantities of coffee or tea (Caffeine).
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| Drug Target |
[Drug Target]
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| Description |
Lorazepam¿¡ ´ëÇÑ Description Á¤º¸ A benzodiazepine used as an anti-anxiety agent with few side effects. It also has hypnotic, anticonvulsant, and considerable sedative properties and has been proposed as a preanesthetic agent. [PubChem]
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| Dosage Form |
Lorazepam¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Liquid IntravenousTablet OralTablet Sublingual
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| Drug Category |
Lorazepam¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-anxiety AgentsAnticonvulsantsAntiemeticsBenzodiazepinesGABA ModulatorsHypnotics and Sedatives
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| Smiles String Canonical |
Lorazepam¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ OC1N=C(C2=CC=CC=C2Cl)C2=C(NC1=O)C=CC(Cl)=C2
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| Smiles String Isomeric |
Lorazepam¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ O[C@@H]1N=C(C2=CC=CC=C2Cl)C2=C(NC1=O)C=CC(Cl)=C2
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| InChI Identifier |
Lorazepam¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C15H10Cl2N2O2/c16-8-5-6-12-10(7-8)13(19-15(21)14(20)18-12)9-3-1-2-4-11(9)17/h1-7,15,21H,(H,18,20)/f/h18H
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| Chemical IUPAC Name |
Lorazepam¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 7-chloro-5-(2-chlorophenyl)-3-hydroxy-1,3-dihydro-1,4-benzodiazepin-2-one
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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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