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³ª¹Ì¾ßÅ©¸² NAMIYA CREAM.[Betamethasone dipropionate , Clotrimazole]
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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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[A23401241]
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\0 ¿ø/1g(2006.12.01)(ÇöÀç¾à°¡)
\50 ¿ø/1g(2003.03.01)(º¯°æÀü¾à°¡)
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1CREAM |
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[ÀûÀÀÁõ º° °Ë»ö]
¼ºÈ«»ö ¹é¼±±Õ, ¸ðâ¹é¼±±Õ, À¯¸ðÇ¥ÇÇ»ç»ó±Õ, °³¼ÒÆ÷ÀÚ±Õ¿¡ ÀÇÇÑ . ¼¼ºÎ¹é¼± . °íºÎ¹é¼± . ¹«Á»
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Çϱâ¿Í °°ÀÌ ºÎÀÛ¿ëÀÌ ±¹¼Ò¿ë ºÎ½ÅÇÇÁúȦ¸óÁ¦ÀÇ »ç¿ë¿¡¼ º¸°íµÈ ¹Ù ÀÖÀ¸¸ç ¹ÐºÀ ºØ´ë¿ä¹ý¿¡¼ ½ÉÇÏ°Ô ³ªÅ¸³½´Ù. Clotrimazole »ç¿ëÀ¸·Î º¸°íµÈ ºÎÀÛ¿ë, È«¹Ý, â»ó, ¼öÆ÷, ÇǺιڸ®, ºÎÁ¾, ¼Ò¾çÁõ, ´ã¸¶Áø°ú ÀϹÝÀûÀÎ ¿ÁõµîÀÌ ÀÖ´Ù.
Betametascne dipropiomate»ç¿ëÀ¸·Î º¸°íµÈ ºÎÀÛ¿ë
ÀÛ¿°¨, °¡·Á¿òÁõ, Àڱذ¨, °ÇÁ¶, ¸ð³¶¿°, ´Ù¸ðÁõ, ¿©µå¸§¾ç¹ßÁø,»ö¼ÒÄ§ÂøºÎ ÀüÁõ,±¸°ÁÖÀ§ ÇǺο°, ¾Ë·¯Áö¼º Á¢Ã˼ºÇǺο°, ÇǺÎħ¿°, ÀÌÂ÷°¨¿°, ¼±Á¶Áõ ¹× ÇÑÁø
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| Off-label Usage |
[Á¶È¸]
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| Related FDA Approved Drug |
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µå·°ÀÎÆ÷ ÀǾàǰ ¿ä¾à/»ó¼¼Á¤º¸
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 FDA : Cµî±Þ
(betamethasone topical )
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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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| DUR (ÀǾàǰ»ç¿ëÆò°¡) |
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| Mechanism of Action |
Betamethasone¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Betamethasone is a glucocorticoid receptor agonist. The antiinflammatory actions of corticosteroids are thought to involve lipocortins, phospholipase A2 inhibitory proteins which, through inhibition arachidonic acid, control the biosynthesis of prostaglandins and leukotrienes. The immune system is suppressed by corticosteroids due to a decrease in the function of the lymphatic system, a reduction in immunoglobulin and complement concentrations, the precipitation of lymphocytopenia, and interference with antigen-antibody binding. Betamethasone binds to plasma transcortin, and it becomes active when it is not bound to transcortin.
Clotrimazole¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Clotrimazole interacts with yeast 14-¥á demethylase, a cytochrome P-450 enzyme that converts lanosterol to ergosterol, an essential component of the membrane. In this way, clotrimazole inhibits ergosterol synthesis, resulting in increased cellular permeability. Clotrimazole may also inhibit endogenous respiration, interact with membrane phospholipids, inhibit the transformation of yeasts to mycelial forms and the uptake of purine, impair triglyceride and/or phospholipid biosynthesis, and inhibit the movement of calcium and potassium ions across the cell membrane by blocking the ion transport pathway known as the Gardos channel.
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| Pharmacology |
Betamethasone¿¡ ´ëÇÑ Pharmacology Á¤º¸ Betamethasone and its derivatives, betamethasone sodium phosphate and betamethasone acetate, are synthetic glucocorticoids. Used for its antiinflammatory or immunosuppressive properties, betamethasone is combined with a mineralocorticoid to manage adrenal insufficiency and is used in the form of betamethasone benzoate, betamethasone dipropionate, or betamethasone valerate for the treatment of inflammation due to corticosteroid-responsive dermatoses. Betamethasone and clotrimazole are used together to treat cutaneous tinea infections.
Clotrimazole¿¡ ´ëÇÑ Pharmacology Á¤º¸ Clotrimazole, an imidazole derivative with a broad spectrum of antimycotic activity, inhibits biosynthesis of the sterol ergostol, an important component of fungal cell membranes. Its action leads to increased membrane permeability and apparent disruption of enzyme systems bound to the membrane. Betamethasone and clotrimazole are used together to treat cutaneous tinea infections. In studies in fungal cultures, the minimum fungicidal concentration of clotrimazole caused leakage of intracellular phosphorous compounds into the ambient medium with concomitant breakdown of cellular nucleic acids, and accelerated potassium etflux. Both of these events began rapidly and extensively after addition of the drug to the cultures. The primary action of clotrimazole is against dividing and growing organisms.
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| Metabolism |
Betamethasone¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 3A4 (CYP3A4)
Clotrimazole¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 11A1 (CYP11A1)Cytochrome P450 1A2 (CYP1A2)Cytochrome P450 2D6 (CYP2D6)
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| Protein Binding |
Betamethasone¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 64%
Clotrimazole¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 90%
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| Half-life |
Betamethasone¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 5.6 hours
Clotrimazole¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 2 hours
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| Absorption |
Betamethasone¿¡ ´ëÇÑ Absorption Á¤º¸ Minimal if applied topically.
Clotrimazole¿¡ ´ëÇÑ Absorption Á¤º¸ Poorly and erratically absorbed orally, minimal vaginal or topical absorption.
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| Pharmacokinetics |
Betamethasone dipropionateÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- ´Ü¹é°áÇÕ : 64%
- ´ë»ç : ´ëºÎºÐ °£¿¡¼ ´ë»çµÈ´Ù.
- ¹Ý°¨±â : 6.5½Ã°£
- ÃÖ´ëÈ¿°ú ¹ßÇö½Ã°£ : Á¤¸ÆÁÖ»ç : 10¡36ºÐ À̳»
- ¼Ò½Ç : Åõ¿©·®ÀÇ 5% ¹Ì¸¸ÀÌ ¹Ìº¯Èü·Î ½Å¹è¼³
ClotrimazoleÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- Èí¼ö : ¿Ü¿ë : Á¤»ó ÇǺθ¦ ÅëÇØ¼´Â °ÅÀÇ Èí¼öµÇÁö ¾Ê´Â´Ù.
- Ç÷ÁßÃÖ°í³óµµ µµ´Þ½Ã°£ :
- Troches : Ÿ¾× ³óµµ : 3½Ã°£ À̳»
- Áú Å©¸² : Áú³» ³óµµ : 8-24 ½Ã°£ À̳»
- ÁúÁ¤ : Áú³» ³óµµ : 1-2 ÀÏ À̳»
- ¼Ò½Ç : ´ë»çü·Î ´ãÁó¹è¼³
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| Biotransformation |
Betamethasone¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic
Clotrimazole¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic (metabolized to inactive metabolites)
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| Toxicity |
Betamethasone¿¡ ´ëÇÑ Toxicity Á¤º¸ Symptoms of overdose include burning, itching, irritation, dryness, folliculitis, hypertrichosis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, maceration of the skin, secondary infection, skin atrophy, striae, and miliaria.
Clotrimazole¿¡ ´ëÇÑ Toxicity Á¤º¸ Symptoms of overdose include erythema, stinging, blistering, peeling, edema, pruritus, urticaria, burning, and general irritation of the skin, and cramps.
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| Drug Interactions |
Betamethasone¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Ambenonium The corticosteroid decreases the effect of anticholinesterasesEdrophonium The corticosteroid decreases the effect of anticholinesterasesPyridostigmine The corticosteroid decreases the effect of anticholinesterasesAnisindione The corticosteroid alters the anticoagulant effectDicumarol The corticosteroid alters the anticoagulant effectAcenocoumarol The corticosteroid alters the anticoagulant effectWarfarin The corticosteroid alters the anticoagulant effectAspirin The corticosteroid decreases the effect of salicylatesBismuth Subsalicylate The corticosteroid decreases the effect of salicylatesAmobarbital The barbiturate decreases the effect of the corticosteroid Aprobarbital The barbiturate decreases the effect of the corticosteroidButalbital The barbiturate decreases the effect of the corticosteroidButabarbital The barbiturate decreases the effect of the corticosteroidButethal The barbiturate decreases the effect of the corticosteroidDihydroquinidine barbiturate The barbiturate decreases the effect of the corticosteroidHeptabarbital The barbiturate decreases the effect of the corticosteroidHexobarbital The barbiturate decreases the effect of the corticosteroidMethohexital The barbiturate decreases the effect of the corticosteroidMethylphenobarbital The barbiturate decreases the effect of the corticosteroidPentobarbital The barbiturate decreases the effect of the corticosteroidPhenobarbital The barbiturate decreases the effect of the corticosteroidPrimidone The barbiturate decreases the effect of the corticosteroidQuinidine barbiturate The barbiturate decreases the effect of the corticosteroidSecobarbital The barbiturate decreases the effect of the corticosteroidTalbutal The barbiturate decreases the effect of the corticosteroidEthotoin The enzyme inducer decreases the effect of the corticosteroidFosphenytoin The enzyme inducer decreases the effect of the corticosteroidMephenytoin The enzyme inducer decreases the effect of the corticosteroidPhenytoin The enzyme inducer decreases the effect of the corticosteroidRifampin The enzyme inducer decreases the effect of the corticosteroidMidodrine Increased arterial pressureSalicylate-magnesium The corticosteroid decreases the effect of salicylatesSalicylate-sodium The corticosteroid decreases the effect of salicylatesSalsalate The corticosteroid decreases the effect of salicylatesTrisalicylate-choline The corticosteroid decreases the effect of salicylates
Clotrimazole¿¡ ´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 |
Betamethasone¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take with food to reduce irritation.
Clotrimazole¿¡ ´ëÇÑ Food Interaction Á¤º¸ Not Available
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| Drug Target |
[Drug Target]
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| Description |
Betamethasone¿¡ ´ëÇÑ Description Á¤º¸ A glucocorticoid given orally, parenterally, by local injection, by inhalation, or applied topically in the management of various disorders in which corticosteroids are indicated. Its lack of mineralocorticoid properties makes betamethasone particularly suitable for treating cerebral edema and congenital adrenal hyperplasia. (From Martindale, The Extra Pharmacopoeia, 30th ed, p724)
Clotrimazole¿¡ ´ëÇÑ Description Á¤º¸ An imidazole derivative with a broad spectrum of antimycotic activity. It inhibits biosynthesis of the sterol ergostol, an important component of fungal cell membranes. Its action leads to increased membrane permeability and apparent disruption of enzyme systems bound to the membrane. [PubChem]
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| Dosage Form |
Betamethasone¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Cream TopicalEnema TopicalLotion TopicalOintment Topical
Clotrimazole¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Cream IntravaginalCream Topical
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| Drug Category |
Betamethasone¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Asthmatic AgentsAnti-inflammatory AgentsAnti-inflammatory, steroidalCorticosteroidGlucocorticoidsImmunosuppressive Agents
Clotrimazole¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Infective Agents, LocalAntifungal AgentsGrowth Inhibitors
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| Smiles String Canonical |
Betamethasone¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC1CC2C3CCC4=CC(=O)C=CC4(C)C3(F)C(O)CC2(C)C1(O)C(=O)CO
Clotrimazole¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ ClC1=CC=CC=C1C(N1C=CN=C1)(C1=CC=CC=C1)C1=CC=CC=C1
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| Smiles String Isomeric |
Betamethasone¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(O)C(=O)CO
Clotrimazole¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ ClC1=CC=CC=C1C(N1C=CN=C1)(C1=CC=CC=C1)C1=CC=CC=C1
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| InChI Identifier |
Betamethasone¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C22H29FO5/c1-12-8-16-15-5-4-13-9-14(25)6-7-19(13,2)21(15,23)17(26)10-20(16,3)22(12,28)18(27)11-24/h6-7,9,12,15-17,24,26,28H,4-5,8,10-11H2,1-3H3/t12-,15-,16-,17-,19-,20-,21-,22-/m0/s1
Clotrimazole¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C22H17ClN2/c23-21-14-8-7-13-20(21)22(25-16-15-24-17-25,18-9-3-1-4-10-18)19-11-5-2-6-12-19/h1-17H
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| Chemical IUPAC Name |
Betamethasone¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-3-one
Clotrimazole¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 1-[(2-chlorophenyl)-di(phenyl)methyl]imidazole
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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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