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±¤µ¿¸¶½ºÅõ¿¡½º¿¬°í KWANGDONG MASTU S OINT.[Bismuth subgallate , Bufexamac , Lidocaine Hydrochloride , Titanium dioxide]
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ÀϹÝÀǾàǰ | ºñ±Þ¿©
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¼öÀÔÀǾàǰ
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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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û±¸ÄÚµå(KDÄÚµå) ºñ±Þ¿©Á¡°ËÄÚµå »óÇÑ±Ý¾× |
ºñ±Þ¿©
[»óº´ÄÚµåÁ¶È¸]
[Áúº´ÄÚµåÁ¶È¸]
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| Á¦Ç°¼º»ó |
¿¯Àº Ȳ»öÀ» ¶í ¿¬°íÁ¦ [Á¦ÇüÁ¤º¸ È®ÀÎ] |
| Æ÷À塤À¯Åë´ÜÀ§ |
20g, 1EA |
| È¿´ÉÈ¿°ú |
[ÀûÀÀÁõ º° °Ë»ö]
1±â ¹× 2±â Ä¡ÇÙ, Ä¡¿, ±Þ ¡¤¸¸¼º Ç×¹®½ÀÁø, Á÷Àå¿°
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| ¿ë¹ý¿ë·® |
* Àý´ë ÀÓÀǺ¹¿ëÇÏÁö ¸¶½Ã°í ¹Ýµå½Ã ÀÇ»ç ¶Ç´Â ¾à»ç¿Í »ó´ãÇϽñ⠹ٶø´Ï´Ù.
[󹿾à¾î]
- ¿ÜºÎ¿¡ Àû¿ë½Ã: 1ÀÏ 2ȸ ȯºÎ¿¡ ¹Ù¸¥ ÈÄ ¸¶»çÁöÇÏµí °¡º±°Ô ¹®Áú·¯ ÁØ´Ù.
- Á÷Àå³» Åõ¿©½Ã: ÁÖÀԱ⸦ ÀÌ¿ëÇÏ¿© 1ÀÏ 2ȸ Á÷Àå ³» »ðÀÔÇÑ´Ù.
[Á¦Çüº°º¹¾àÁöµµ]
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| ½ÅÁßÅõ¿© |
¼Ò¾Æ ¹× û¼Ò³â |
| ÀÌ»ó¹ÝÀÀ |
- ÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
- µå¹°°Ô ¼öÆ÷, ½É¿ï, ³«¼³, ±¸¹Ý µîÀ» ¼ö¹ÝÇÑ È¯ºÎÀÇ ºÎÁ¾ÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¸ç µå¹°°Ô ³ÐÀº ºÎÀ§¿¡ °ÉÃÄ ½ÉÇÏ°Ô ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
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| »óÈ£ÀÛ¿ë |
- ´Ù¸¥ ¾à¹°°ú º´¿ëÅõ¿©½Ã ºÎÀÛ¿ë µîÀÇ ¹ß»ýÀº º¸°íµÈ ¹Ù ¾ø´Ù.
- º»Á¦´Â Äܵ¼, Áú³» ÇÇÀÓ¿ë°Ý¸·°ú °°Àº ¶óµ¦½º ¶Ç´Â °í¹«Á¦Ç°À» ¾àȽÃų ¼ö ÀÖÀ¸¹Ç·Î ÁÖÀÇÇÑ´Ù.
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| Off-label Usage |
[Á¶È¸]
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| Related FDA Approved Drug |
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 | Á¤º¸¿ä¾à |
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µå·°ÀÎÆ÷ ÀǾàǰ ¿ä¾à/»ó¼¼Á¤º¸
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³»¿ë |
| BIT ¾àÈ¿ºÐ·ù |
Ç÷°ü°ÈÁ¦, Á¤¸Æ·ù Ä¡·áÁ¦, Ä¡Áú¾à(Capillary stabilizer, Phlebitis, Varicose veins, Hemorrhoidal)
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| ATC ÄÚµå |
Local anesthetics / C05AD
[ÄÚµåºÐ·ù»ó¼¼¼³¸í]
[ATCÄÚµå¿¹Ãø]
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| º¹ÁöºÎºÐ·ùÄÚµå |
256 (Ä¡Áú¿ëÁ¦ )
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| Drugs By Indication |
[Àüüº¸±â]
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| Drugs By Classification |
[Àüüº¸±â]
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| LACTmed ¹Ù·Î°¡±â |
[¹Ù·Î°¡±â]
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À¯·áÁ¤º¸ÀÔ´Ï´Ù.
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ÀüüÀӽŠ±â°£º°·Î ¿©·¯µî±ÞÀÌ Á¸ÀçÇÒ ¼ö ÀÖÀ¸¸ç °¡Àå À§Çèµµ°¡ ³ôÀº Á¤º¸¸¸ º¸¿©Áý´Ï´Ù. ´Ü, º¹ÇÕÁ¦ÀÇ °æ¿ì ¸ðµç º¹ÇÕÁ¦¼ººÐ¿¡ ´ëÇÑ ÀÓºÎÅõ¿©µî±ÞÀÌ Ç¥½ÃµÈ°ÍÀº Àý´ë ¾Æ´Ï¸ç Ç¥½ÃµÈ°ÍÁß¿¡ °¡Àå À§Çèµµ°¡ ³ôÀº Á¤º¸¸¸ ³ªÅ¸³³´Ï´Ù.
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»ó±â ÀÓºÎÅõ¿©¿¡ ´ëÇÑ Á¤º¸´Â Àü»êó¸® µÇ¸é¼ ÀÔ·Â ¿À·ù °¡´É¼ºÀÌ Á¸ÀçÇÕ´Ï´Ù. ¿À·ù °¡´É¼ºÀ» ÃÖ¼ÒÈÇϱâ À§ÇÏ¿© ¸¹Àº ³ë·ÂÀ» ±â¿ïÀ̰í ÀÖÀ¸³ª, ±× Á¤È®¼º¿¡ ´ëÇÏ¿© È®½ÅÀ» µå¸± ¼ö ¾ø½À´Ï´Ù. ÀÌ¿¡ ´ëÇØ ȸ»ç´Â Ã¥ÀÓÀ» ÁöÁö ¾Ê½À´Ï´Ù.
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¹Ýµå½Ã °ø½Å·Â ÀÖ´Â ¹®ÇåÀ» ´Ù½Ã Çѹø Âü°í ÇϽñ⠹ٶó¸ç ÀÇ»ç ¶Ç´Â ¾à»çÀÇ ÆÇ´Ü¿¡ µû¶ó Åõ¿©¿©ºÎ°¡ °áÁ¤µÇ¾î¾ß ÇÕ´Ï´Ù.
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½ÅÀå¾Ö, °£Àå¾Ö½Ã ¿ë·®Á¶Àý |
À¯·áÁ¤º¸ÀÔ´Ï´Ù.
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| Pharmacokinetics |
À¯·áÁ¤º¸ÀÔ´Ï´Ù.
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| º´¿ë±Ý±â ¹× ¿¬·É´ë±Ý±â ±Ù°ÅÁ¶È¸ |
[º´¿ë±Ý±â ¹× ¿¬·É´ë±Ý±â ±Ù°ÅÁ¶È¸]
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| Á¦Çüº° º¹¾àÁöµµ |
[¿¬°í] |
| º¸°ü»ó ÁÖÀÇ |
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| Á¶Á¦½Ã ÁÖÀÇ |
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| Ç׸ñ |
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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]
¿¬·É´ë±Ý±â :
°í½ÃµÈ ¿¬·É±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
[¿¬·É´ë±Ý±â»ó¼¼°Ë»ö]
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| µ¶¼ºÁ¤º¸ |
Lidocaine¿¡ ´ëÇÑ µ¶¼ºÁ¤º¸ : Á¤º¸º¸±â
Titanium¿¡ ´ëÇÑ µ¶¼ºÁ¤º¸ : Á¤º¸º¸±â
Titanium dioxide¿¡ ´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 |
Lidocaine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Lidocaine stabilizes the neuronal membrane by inhibiting the ionic fluxes required for the initiation and conduction of impulses thereby effecting local anesthetic action.
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| Pharmacology |
Lidocaine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Lidocaine is an anesthetic agent indicated for production of local or regional anesthesia and in the treatment of ventricular tachycardia occurring during cardiac manipulation, such as surgery or catheterization, or which may occur during acute myocardial infarction, digitalis toxicity, or other cardiac diseases. The mode of action of the antiarrhythmic effect of Lidocaine appears to be similar to that of procaine, procainamide and quinidine. Ventricular excitability is depressed and the stimulation threshold of the ventricle is increased during diastole. The sinoatrial node is, however, unaffected. In contrast to the latter 3 drugs, Lidocaine in therapeutic doses does not produce a significant decrease in arterial pressure or in cardiac contractile force. In larger doses, lidocaine may produce circulatory depression, but the magnitude of the change is less than that found with comparable doses of procainamide.
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| Metabolism |
Lidocaine¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 1A2 (CYP1A2)Cytochrome P450 2D6 (CYP2D6)
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| Protein Binding |
Lidocaine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 60-80%
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| Half-life |
Lidocaine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 109 minutes
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| Absorption |
Lidocaine¿¡ ´ëÇÑ Absorption Á¤º¸ Information derived from diverse formulations, concentrations and usages reveals that lidocaine is completely absorbed following parenteral administration, its rate of absorption depending, for example, upon various factors such as the site of administration and the presence or absence of a vasoconstrictor agent.
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| Pharmacokinetics |
Lidocaine HydrochlorideÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- È¿°ú¹ßÇö½Ã°£ (1ȸ bolus ¿ë·®À¸·Î¼) : 45-90ÃÊ
- ÀÛ¿ëÁö¼Ó½Ã°£ : 10-25ºÐ
- ºÐÆ÷ (Vd) : ¸¹Àº ¿äÀο¡ µû¶ó º¯ÈµÇ¸ç, ¿ïÇ÷¼º ½ÉºÎÀü°ú °£Áúȯ¿¡¼´Â ºÐÆ÷¿ëÀûÀÌ °¨¼ÒµÊ
- ´Ü¹é°áÇÕ : 60-80%, ¥á1-acid glycoprotein°ú °áÇÕ
- ´ë»ç : °£¿¡¼ 90% ´ë»ç
- Ȱ¼ºÇü ´ë»çüÀÎ monoethylglycinexylidide(MEGX)¿Í glycinexylidide(GX)°¡ ÃàÀûµÇ¾î ÁßÃ߽Űæ°è µ¶¼ºÀ» À¯¹ßÇÒ ¼ö ÀÖ´Ù.
- ¹Ý°¨±â (biphasic) : ¿ïÇ÷¼º ½ÉºÎÀü, °£Áúȯ, ¼îÅ©, ÁßÁõÀÇ ½ÅÁúȯ¿¡¼ Áõ°¡
- Ãʱâ : 7-30ºÐ
- ¸»±â : ¿µ¾Æ, ¹Ì¼÷¾Æ : 3.2½Ã°£, ¼ºÀÎ : 1.5-2½Ã°£
BufexamacÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- Èí¼ö : °æ±¸·Î Åõ¿©ÇßÀ» °æ¿ì, ºü¸£°í, °ÅÀÇ 100 %Èí¼öµÈ´Ù.
±¹¼ÒÁ¦Á¦ÀÇ °æ¿ì, ¸Å°³Ã¼¿¡ µû¶ó ´Ù¸£´Ù.
- ´ë»ç : Æ÷ÇÕ¹ÝÀÀÀ» ÅëÇØ ´ë»çµÇ¾î BPAA(p-n-Butoxyphenylacetic acid), HPA(p-hydroxyphenylacetic acid)·Î ´ë»çµÈ´Ù.
- ½Å¹è¼³ : ´ë»çü 75%, ¸ð¾à¹° 1%
¸ð¾à¹°ÀÇ elimination half life´Â 3½Ã°£ÀÌ´Ù.
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| Biotransformation |
Lidocaine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Primarily hepatic.
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| Toxicity |
Lidocaine¿¡ ´ëÇÑ Toxicity Á¤º¸ The oral LD 50 of lidocaine HCl in non-fasted female rats is 459 (346-773) mg/kg (as the salt) and 214 (159-324) mg/kg (as the salt) in fasted female rats. Symptoms of overdose include convulsions, hypoxia, acidosis, bradycardia, arrhythmias and cardiac arrest.
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| Drug Interactions |
Bismuth¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Acetazolamide The salicylate at high dose increases the effect of the carbonic anhydrase inhibitorsAcetohexamide The salicylate increase the effect of sulfonylureaMethotrexate The salicylate increase the effect and toxicity of methotrexateAnisindione The salicylate increase effect of anticoagulantBetamethasone The corticosteroid decreases the effect of salicylatesChlorpropamide The salicylate increase the effect of sulfonylureaCortisone acetate The corticosteroid decreases the effect of salicylatesDemeclocycline Formation of non-absorbable complexesDexamethasone The corticosteroid decreases the effect of salicylatesDichlorphenamide The salicylate at high dose increases the effect of the carbonic anyhydrase inhibitorsDicumarol The salicylate increase effect of anticoagulantValproic Acid The salicylate increase the effect of valproic acidDoxycycline Formation of non absorbable complexesFludrocortisone The corticosteroid decreases the effect of salicylatesGliclazide The salicylate increase the effect of sulfonylureaGlipizide The salicylate increase the effect of sulfonylureaGlisoxepide The salicylate increase the effect of sulfonylureaGlibenclamide The salicylate increase the effect of sulfonylureaGlycodiazine The salicylate increase the effect of sulfonylureaHydrocortisone The corticosteroid decreases the effect of salicylatesInsulin The salicylate increase the effect of insulinInsulin-aspart The salicylate increase the effect of insulinInsulin-detemir The salicylate increase the effect of insulinInsulin-glargine The salicylate increase the effect of insulinInsulin-glulisine The salicylate increase the effect of insulinInsulin-lispro The salicylate increase the effect of insulinMethacycline Formation of non absorbable complexesMethazolamide The salicylate at high dose increases the effect of the carbonic anhydrase inhibitorsMethylprednisolone The corticosteroid decreases the effect of salicylatesMinocycline Formation of non-absorbable complexesAcenocoumarol The salicylate increases effect of anticoagulantOxytetracycline Formation of non-absorbable complexesParamethasone The corticosteroid decreases the effect of salicylatesPrednisolone The corticosteroid decreases the effect of salicylatesPrednisone The corticosteroid decreases the effect of salicylatesProbenecid The salicylate decreases the uricosuric effect of probenecidSulfinpyrazone The salicylate antagonizes the uricosuric effect of sulfinpyrazoneTetracycline Formation of non-absorbable complexesTolazamide The salicylate increase the effect of sulfonylureaTolbutamide The salicylate increase the effect of sulfonylureaTriamcinolone The corticosteroid decreases the effect of salicylatesWarfarin The salicylate increases effect of anticoagulant
Lidocaine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Bismuth¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take without regard to meals.
Lidocaine¿¡ ´ëÇÑ Food Interaction Á¤º¸ Not Available
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| Drug Target |
[Drug Target]
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| Description |
Bismuth¿¡ ´ëÇÑ Description Á¤º¸ Bismuth compounds are widely used for the treatment of peptic ulcers and Helicobacter pylori infections. It has been suggested that enzyme inhibition plays an important role in the antibacterial activity of bismuth towards this bacterium. Bismuth thiols appear to act on bacterial ureases.
Lidocaine¿¡ ´ëÇÑ Description Á¤º¸ A local anesthetic and cardiac depressant used as an antiarrhythmia agent. Its actions are more intense and its effects more prolonged than those of procaine but its duration of action is shorter than that of bupivacaine or prilocaine. [PubChem]
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| Dosage Form |
Bismuth¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Dressing TopicalLiquid OralLiquid SublingualSolution / drops OralSuppository RectalSuspension OralTablet Oral
Lidocaine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Aerosol TopicalAerosol, metered TopicalCream TopicalGel TopicalJelly TopicalJelly UrethralLiquid BuccalLiquid DentalLiquid InfiltrationLiquid IntravenousLiquid OralLiquid TopicalLotion TopicalOintment TopicalSolution InfiltrationSolution IntramuscularSolution IntravenousSolution OralSolution TopicalSpray TopicalSwab Topical
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| Drug Category |
Bismuth¿¡ ´ëÇÑ Drug_Category Á¤º¸ Antidiarrheals
Lidocaine¿¡ ´ëÇÑ Drug_Category Á¤º¸ AnestheticsAnesthetics, LocalAnti-Arrhythmia AgentsAntiarrhythmic Agents
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| Smiles String Canonical |
Bismuth¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ O.O=C1O[Bi]OC2=CC=CC=C12
Lidocaine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CCN(CC)CC(=O)NC1=C(C)C=CC=C1C
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| Smiles String Isomeric |
Bismuth¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ O.O=C1O[Bi]OC2=CC=CC=C12
Lidocaine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CCN(CC)CC(=O)NC1=C(C)C=CC=C1C
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| InChI Identifier |
Bismuth¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C7H6O3.Bi.H2O/c8-6-4-2-1-3-5(6)7(9)10;;/h1-4,8H,(H,9,10);;1H2/q;+2;/p-2/fC7H4O3.Bi.H2O/h8h;;/q-2;m;/rC7H4BiO3.H2O/c9-7-5-3-1-2-4-6(5)10-8-11-7;/h1-4H;1H2
Lidocaine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C14H22N2O/c1-5-16(6-2)10-13(17)15-14-11(3)8-7-9-12(14)4/h7-9H,5-6,10H2,1-4H3,(H,15,17)/f/h15H
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| Chemical IUPAC Name |
Bismuth¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 3,5-dioxa-4$l^{2}-bismabicyclo[4.4.0]deca-1(10),6,8-trien-2-one hydrate
Lidocaine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 2-diethylamino-N-(2,6-dimethylphenyl)acetamide
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| Drug-Induced Toxicity Related Proteins |
DOCA ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸ Replated Protein:Aquaporin-2 Drug:DOCA Toxicity:hypertension. [¹Ù·Î°¡±â] LIDOCAINE ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸ Replated Protein:glucose-regulated protein Drug:lidocaine Toxicity:intestinal disorder. [¹Ù·Î°¡±â] Replated Protein:Alkaline phosphatase Drug:lidocaine Toxicity:lidocaine induced hepatitis. [¹Ù·Î°¡±â] Replated Protein:C-reactive protein Drug:lidocaine Toxicity:fever. [¹Ù·Î°¡±â] Replated Protein:C-reactive protein Drug:lidocaine Toxicity:lidocaine induced hepatitis. [¹Ù·Î°¡±â] Replated Protein:Alpha-1-acid glycoprotein Drug:lidocaine Toxicity:lidocaine tolerance. [¹Ù·Î°¡±â] Replated Protein:Gamma-glutamyltranspeptidase Drug:lidocaine Toxicity:fever. [¹Ù·Î°¡±â] Replated Protein:Alkaline phosphatase Drug:lidocaine Toxicity:fever. [¹Ù·Î°¡±â] Replated Protein:Gamma-glutamyltranspeptidase Drug:lidocaine Toxicity:lidocaine induced hepatitis. [¹Ù·Î°¡±â]
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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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