Dexbrompheniramine

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Dexbrompheniramine
Dexbrompheniramine.svg
Clinical data
Trade names Drixoril, Conex, Dixaphedrine
AHFS/Drugs.com Multum Consumer Information
Routes of
administration
Oral
ATC code
Legal status
Legal status
Pharmacokinetic data
Elimination half-life 25 hours
Identifiers
  • (3S)-3-(4-bromophenyl)-N,N-dimethyl-3-pyridin-2-yl-propan-1-amine
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard 100.004.595 OOjs UI icon edit-ltr-progressive.svg
Chemical and physical data
Formula C16H19BrN2
Molar mass 319.246 g·mol−1
3D model (JSmol)
  • Brc1ccc(cc1)[C@@H](c2ncccc2)CCN(C)C
  • InChI=1S/C16H19BrN2/c1-19(2)12-10-15(16-5-3-4-11-18-16)13-6-8-14(17)9-7-13/h3-9,11,15H,10,12H2,1-2H3/t15-/m0/s1 Yes check.svgY
  • Key:ZDIGNSYAACHWNL-HNNXBMFYSA-N Yes check.svgY
 X mark.svgNYes check.svgY  (what is this?)    (verify)

Dexbrompheniramine is an antihistamine with anticholinergic properties [1] used to treat allergic conditions such as hay fever or urticaria. It is the pharmacologically active dextrorotatory isomer of brompheniramine. It was formerly marketed in combination with pseudoephedrine under the name Drixoral in the US and Canada. It is an alkylamine antihistamine.

Contents

Dexbrompheniramine is a first generation antihistamine that reduces the effects of the neurotransmitter histamine in the body; sneezing, itching, watery eyes, and runny nose.

Interactions

MAO inhibitors within 14 days. MAO inhibitors include isocarboxazid, linezolid, phenelzine, rasagiline, selegiline, and tranylcypromine.

Potassium

Drinking alcohol can increase side effects of dexbrompheniramine.

Related Research Articles

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References

  1. Löfkvist T (1978). "A comparative evaluation of oral decongestants in the treatment of vasomotor rhinitis". The Journal of International Medical Research. 6 (1): 56–60. doi:10.1177/030006057800600110. PMID   627306. S2CID   39205584.