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DM defined medium; dermatomyositis; Descemet's membrane; dextromaltose; dextromethorphan; diabetes mell...
PE Edinburgh Pharmacopoeia; pancreatic extract; paper electrophoresis; partial epilepsy; pelvic examina...
PHE periodic health examination; phenylephrine
syr. syrupus; syrup
MSU maple sugar urine; maple syrup urine; medical studies unit; mid-stream urine; monosodium urate; myoc...
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Dex Dextromethorphan
HFCS High-Fructose Corn Syrup
MSUD Maple Syrup Urine Disease
PE Phenylephrine
PHE Phenylephrine
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phenylephrine <chemical> An alpha-adrenergic agonist used as a mydriatic, nasal decongestant, and cardiotonic agent.
Pharmacological action: adrenergic alpha-agonists, cardiotonic agent, mydriatics, nasal decongestants, sympathomimetic, vasoconstrictor agents.
Chemical name: Benzenemethanol, 3-hydroxy-alpha-((methylamino)methyl)-, (R)-
(12 Dec 1998)
phenylephrine hydrochloride <drug> An alpha 1 adrenergic agonist.
(15 Oct 1997)
pyrilamine <chemical> A histamine h1 antagonist. It has mild hypnotic properties and some local anaesthetic action and is used for allergies (including skin eruptions) both parenterally and locally. It is a common ingredient of cold remedies.
Pharmacological action: anti-allergic agents, histamine h1 antagonists.
Chemical name: 1,2-Ethanediamine, N-((4-methoxyphenyl)methyl)-N',N'-dimethyl-N-2-pyridinyl-
(12 Dec 1998)
pyrilamine maleate 2-[(2-dimethylaminoethyl) (p-methoxybenzyl)amino]pyridine maleate;an antihistaminic.
Synonym: mepyramine maleate.
(05 Mar 2000)
dextromethorphan <chemical> The d-isomer of the codeine analog of levorphanol. It acts on the medullary cough centre to suppress cough but does not have the addictive, analgesic, and sedative effects of codeine and does not produce respiratory depression at usual doses.
Pharmacological action: antitussive agents.
Chemical name: Morphinan, 3-methoxy-17-methyl-, (9alpha,13alpha,14alpha)-
(12 Dec 1998)
dextromethorphan hydrobromide Hydrobromide of d-racemethorphan; d-3-methoxy-N-methylmorphinan hydrobromide;a synthetic morphine derivative used as an antitussive agent. It has weak central depressant action, and appears to have little addiction liability.
(05 Mar 2000)
dextromethorphan O-demethylase <enzyme> Cytochrome p450iid6 is the specific cytochrome used for the enzymatic reaction
Registry number: EC 1.-
(26 Jun 1999)
maple syrup urine See: maple syrup urine disease.
(05 Mar 2000)
maple syrup urine disease Hereditary disease due to deficiency of an enzyme involved in amino acid metabolism, characterised by urine that smells like maple syrup.
(12 Dec 1998)
syrup 1. A thick and viscid liquid made from the juice of fruits, herbs, etc, boiled with sugar.
2. A thick and viscid saccharine solution of superior quality (as sugarhouse sirup or molasses, maple sirup); specifically, in pharmacy and often in cookery, a saturated solution of sugar and water (simple sirup), or such a solution flavored or medicated. "Lucent sirups tinct with cinnamon." (Keats) Mixing sirup. See the Note under Dextrose.
Origin: F. Sirop (cf. It. Siroppo, Sp. Jarabe, jarope, LL. Siruppus, syrupus), fr. Ar. Sharab a drink, wine, coffee, sirup. Cf. Sherbet.
Source: Websters Dictionary
(01 Mar 1998)
disease, maple syrup urine Hereditary disease due to deficiency of an enzyme involved in amino acid metabolism, characterised by urine that smells like maple syrup.
(12 Dec 1998)
ipecac syrup A sweetened liquid medicinal preparation containing powdered ipecac extract, which contains the alkaloids emetine and cephaline; used as an emetic in certain cases of poisoning and (at lower doses) as an expectorant.
(05 Mar 2000)
ipecac (syrup) <chemical> A syrup made from the dried rhizomes of two different species, c. Ipecacuanha and c. Acuminata of cephaelis (or uragoga) of the rubiaciae; they contain emetine, cephaeline, psychotrine and other isoquinolines. Ipecac syrup is used widely as an emetic acting both locally on the gastric mucosa and centrally on the chemoreceptor trigger zone. It may also be used as an expectorant.
Pharmacological action: emetics, expectorants.
Chemical name: Ipecac
(12 Dec 1998)
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