[{"@context":"http:\/\/schema.org\/","@type":"BlogPosting","@id":"https:\/\/wiki.edu.vn\/all2en\/wiki32\/doxylamine-wikipedia\/#BlogPosting","mainEntityOfPage":"https:\/\/wiki.edu.vn\/all2en\/wiki32\/doxylamine-wikipedia\/","headline":"DOXYLAMINE \u2014 Wikipedia","name":"DOXYLAMINE \u2014 Wikipedia","description":"before-content-x4 A wikipedia article, free l’encyclop\u00e9i. Doxylamine Enantiomer r from doxylamine (left) and S-Doxylamine (right) Identification UICPA name ( RS","datePublished":"2018-07-27","dateModified":"2018-07-27","author":{"@type":"Person","@id":"https:\/\/wiki.edu.vn\/all2en\/wiki32\/author\/lordneo\/#Person","name":"lordneo","url":"https:\/\/wiki.edu.vn\/all2en\/wiki32\/author\/lordneo\/","image":{"@type":"ImageObject","@id":"https:\/\/secure.gravatar.com\/avatar\/44a4cee54c4c053e967fe3e7d054edd4?s=96&d=mm&r=g","url":"https:\/\/secure.gravatar.com\/avatar\/44a4cee54c4c053e967fe3e7d054edd4?s=96&d=mm&r=g","height":96,"width":96}},"publisher":{"@type":"Organization","name":"Enzyklop\u00e4die","logo":{"@type":"ImageObject","@id":"https:\/\/wiki.edu.vn\/wiki4\/wp-content\/uploads\/2023\/08\/download.jpg","url":"https:\/\/wiki.edu.vn\/wiki4\/wp-content\/uploads\/2023\/08\/download.jpg","width":600,"height":60}},"image":{"@type":"ImageObject","@id":"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/a\/ac\/%28%C2%B1%29-Doxylamine_Enantiomers_Structural_Formulae.png\/280px-%28%C2%B1%29-Doxylamine_Enantiomers_Structural_Formulae.png","url":"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/a\/ac\/%28%C2%B1%29-Doxylamine_Enantiomers_Structural_Formulae.png\/280px-%28%C2%B1%29-Doxylamine_Enantiomers_Structural_Formulae.png","height":"184","width":"280"},"url":"https:\/\/wiki.edu.vn\/all2en\/wiki32\/doxylamine-wikipedia\/","wordCount":2435,"articleBody":" (adsbygoogle = window.adsbygoogle || []).push({});before-content-x4A wikipedia article, free l’encyclop\u00e9i. Doxylamine Enantiomer r from doxylamine (left) and S-Doxylamine (right) Identification UICPA name ( RS )- N , N -Dimethyl-2- (1-phenyl-1-pyridin-2-yl-ethoxy) -Tethanamine N O CAS 469-21-6 (Racemic) 76210-49-6 (+) 76210-47-4 ( -) N O Echa 100.006.742 N O THIS 207-414-2 Code ATC R06 AA09 DrugBank DB00366 Pubchem 3162 SMILES Inches Inches: 3D view INCHI = 1\/C17H22N2O\/C1-17 (20-14-13-19 (2) 3,15-9-5-4-6-10-15) 16-11-7-8-18-16\/ H4-12H, 13-14h2,1-3h3 Chemicals Formula C 17 H 22 N 2 O [Isomers] Molar mass [ first ] 270.369 4 \u00b1 0.015 8 g\/mol C\u00a075,52\u00a0%, H\u00a08,2\u00a0%, N\u00a010,36\u00a0%, O\u00a05,92\u00a0%, Physical properties T\u00b0 fusion 25 \u00b0C [ 2 ] Ecotoxicology DL 50 470 mg \u00b7 kg -first (mouse, oral) 62 mg \u00b7 kg -first (mouse, i.v.) 460 mg \u00b7 kg -first (mouse, s.c.) [ 2 ] Pharmacokinetic data Half-life of \u00e9lim. 10h Excretion (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4essentially urinary Therapeutic considerations Therapeutic class Antihistamine h first for systemic use \u2022 sedative Car driving prohibited (level 3) Psychotropic character Category sedative Way of consuming Oral (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4Risk of dependence Weak IS units and CNTP , unless otherwise stated. modifier The doxylamine is an antihistamine h first (Histamine H1 receptor\u00a0 (in) ) first generation; It is used for the treatment of allergies, light insomnia as well as nausea induced by pregnancy [ 3 ] (considered outside the AMM in France). Today first -generation antihistamines are no longer used in first intention to treat allergies, they are preferred to antihistamines of second and third generation specific hints of receptors first peripherals thus eliminating the sedative effect generally unwanted when processing allergies. This is why doxylamine is only indicated in treatment of occasional insomnia. Doxylamine, with significant sedative properties, reduces the sleeping time and avoids night awakenings. Its anti-emotional properties also allow it to be prescribed as anti-nausea. It is used in pyridoxin\/doxylamine combination to treat nausea and vomiting of pregnancy [ 4 ] . (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4A treatment based on doxylamine does not require any prescription, however an extension of treatment beyond five days requires the advice of a doctor. The intake of doxylamine alters the level of vigilance and increases the risk of falling. It makes you unfit for domestic and professional work, as well as to the driving of any vehicle. Doxylamine is classified “A” in terms of its fetal safety by the reference guide Briggs on fetal and neonatal risk [ 5 ] . Although it is customary to say that doxylamine causes no dependence or addiction, it can be nuanced [ 6 ] . Antihistamines h first , or reverse agonist of H receptors first (in) , reduce the effects of histamine. First generation antihistamines are not specific to peripheral receptors, they therefore also act on H receptors first of the central nervous system. \u2191 Molar mass calculated after ‘ Atomic weights of the elements 2007 \u00bb , on www.chem.qmul.ac.uk . \u2191 a et b (in) ‘ Doxylamine \u00bb , on Chedplus , consulted on July 29, 2009 \u2191 ‘ https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/pmc4030125\/ \u00bb , on lecrat.fr (consulted the November 26, 2017 ) \u2191 (in) Svetlana Madjunk , Caroline Maltepe you gideon Koren , ‘ The Delayed-Release Combination of Doxylamine and Pyridoxine (Diclegis\u00ae\/Diclectin\u00ae) for the Treatment of Nausea and Vomiting of Pregnancy \u00bb , Pediatric Drugs , vol. 16, n O 3, first erJune 2014 , p. 199\u2013211 (ISSN\u00a0 1174-5878And 1179-2019, DOI\u00a0 10.1007\/s40272-014-0065-5, read online , consulted the January 16, 2018 ) \u2191 (in) Briggs GG, Freeman RK, Yaffe SJ. Drugs in Pregnancy and Lactation: A Reference Guide to Fetal and Neonatal Risk , 8th edition. 2008. Published by: Lippincott Williams & Wilkins. \u2191 “Dependence is set up (…) with many users. This poses several problems. First, the effectiveness of sedative antihistamines was evaluated in the short term and nothing guarantees their effectiveness beyond a few days or a few weeks, “said Professor Anne Roussin. [Drugs without a prescription, user manual] on Slate.fr of November 12, 2013 (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4"},{"@context":"http:\/\/schema.org\/","@type":"BreadcrumbList","itemListElement":[{"@type":"ListItem","position":1,"item":{"@id":"https:\/\/wiki.edu.vn\/all2en\/wiki32\/#breadcrumbitem","name":"Enzyklop\u00e4die"}},{"@type":"ListItem","position":2,"item":{"@id":"https:\/\/wiki.edu.vn\/all2en\/wiki32\/doxylamine-wikipedia\/#breadcrumbitem","name":"DOXYLAMINE \u2014 Wikipedia"}}]}]