| ¿µ¹® | oral administration | ÇÑ±Û | °æ±¸º¹¿ë |
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| ¿µ¹® | oral cavity | ÇÑ±Û | ±¸° |
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| ¿µ¹® | oral cavity | ÇÑ±Û | ÀÔ¾È |
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| ¼³¸í | ÀÔÀ» ¹ú¿©¼ ÀÔ¼Ó¿¡¼ º¼ ¼ö ÀÖ´Â °ø°£À¸·Î ÀÔõÀå, Æíµµ, ¸ñÁ¥À» º¼ ¼ö ÀÖ´Ù. |
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| CPM | central pontine myelinosis; chlorpheniramine maleate; continuous passive motion; critical path metho... |
|---|---|
| ORS | olfactory reference syndrome; oral rehydration solution; oral surgery, oral surgeon; Orthopaedic Res... |
| BPM | beats per minute; biperidyl mustard; breaths per minute; brompheniramine maleate |
| EM | early memory; ejection murmur; electromagnetic; electron micrograph; electron microscopy, electron m... |
| LHM | lysuride hydrogen maleate |
| CPM | Chlorpheniramine maleate |
|---|---|
| DEM | Diethyl maleate |
| COPV | Canine oral papillomavirus |
| COC | Combined oral contraceptive |
| ORS | G)-oral rehydration solution |
naso-oral
| chlorpheniramine maleate | (±)-2-[p-Chloro-alpha-[2-(dimethylamino)ethyl]benzyl]pyridine maleate;an antihistamine. (05 Mar 2000) |
|---|---|
| chlorpheniramine | <chemical> A histamine h1 antagonist used in allergic reactions, hay fever, rhinitis, urticaria, and asthma. It has also been used in veterinary applications. One of the most widely used of the classical antihistaminics, it generally causes less drowsiness and sedation than promethazine. Pharmacological action: anti-allergic agents, antipruritics, histamine h1 antagonists. Chemical name: 2-Pyridinepropanamine, gamma-(4-chlorophenyl)-N,N-dimethyl- (12 Dec 1998) |
| acetophenazine maleate | 2-Acetyl-103-[4-(2-hydroxyethyl)piperazinyl]propylphenothiazine dimaleate;a phenothiazine tranquilliser. (05 Mar 2000) |
| azatadine maleate | An antihistamine with anticholinergic and antiserotonin properties. Chemical name: 6,11-Dihydro-11-(1-methyl-4-piperidylidene)-5H-benzo[5,6]cyclohepta[1,2-b]pyridine dimaleate. (05 Mar 2000) |
| brompheniramine maleate | 2-[p-Bromo-alpha-(2-dimethylaminoethyl)benzyl]pyridine maleate;a potent antihistaminic agent. (05 Mar 2000) |
| carbinoxamine maleate | Paracarbinoxamine maleate 2-[p-chloro-alpha-(2-dimethylaminoethoxy)benzyl]pyridine maleate; an antihistaminic agent. (05 Mar 2000) |
| maleate | <chemical> The ion from maleic acid, often used in biological buffers. (18 Nov 1997) |
| maleate isomerase | <enzyme> Converts maleate to fumarate; amino acid sequence sourced from from alcaligenes faecalis. Registry number: EC 5.2.1.1 Synonym: maleate cis-trans-isomerase (26 Jun 1999) |
| carphenazine maleate | 110-(3-[4-(2-Hydroxyethyl)-1-piperazinyl]propyl)phenothia zine-2-yl-1-propanone bis(hydrogen maleate);a phenothiazine tranquilliser of the piperazine group. Functionally classified as an antipsychotic agent, it is used in the treatment of chronic and acute schizophrenia; also possesses antiemetic, adrenolytic, anticholinergic, and dopamine-blocking actions. (05 Mar 2000) |
| perhexiline maleate | 2-(2,2-Dicyclohexylethyl)piperidine maleate;a coronary vasodilator and diuretic. (05 Mar 2000) |
| mepyramine maleate | 2-[(2-dimethylaminoethyl) (p-methoxybenzyl)amino]pyridine maleate;an antihistaminic. Synonym: mepyramine maleate. (05 Mar 2000) |
| methylergometrine maleate | D-Lysergic acid-dl-hydroxybutylamide-2 maleate;a partially synthesised derivative of lysergic acid with oxytocic action, used to prevent or treat postpartum uterine atony and haemorrhage. Synonym: methylergometrine maleate. (05 Mar 2000) |
| methylergonovine maleate | D-Lysergic acid-dl-hydroxybutylamide-2 maleate;a partially synthesised derivative of lysergic acid with oxytocic action, used to prevent or treat postpartum uterine atony and haemorrhage. Synonym: methylergometrine maleate. (05 Mar 2000) |
| methysergide maleate | N-[1-(Hydroxymethyl)propyl]-1-methyl-d-lysergamide bimaleate;a serotonin antagonist, weakly adrenolytic, chemically related to methylergonovine; used in the prophylactic treatment of vascular headache (migraine); untoward effects are common. (05 Mar 2000) |
| pheniramine maleate | 1-phenyl-1-(2-pyridyl)-3-dimethylaminopropane maleate;an antihistaminic. Synonym: prophenpyridamine maleate. (05 Mar 2000) |
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