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Pheniramine

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Pheniramine
Clinical data
Pregnancy
category
  • A
Routes of
administration
Oral
ATC code
Pharmacokinetic data
MetabolismHepatic hydroxylation, demethylation and glucuronidation
ExcretionRenal
Identifiers
  • N,N-dimethyl-3-phenyl-3-pyridin-2-yl-propan-1-amine
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.001.506 Edit this at Wikidata
Chemical and physical data
FormulaC16H20N2
Molar mass240.343 g/mol g·mol−1
3D model (JSmol)
  • n1ccccc1C(c2ccccc2)CCN(C)C
  • InChI=1S/C16H20N2/c1-18(2)13-11-15(14-8-4-3-5-9-14)16-10-6-7-12-17-16/h3-10,12,15H,11,13H2,1-2H3 checkY
  • Key:IJHNSHDBIRRJRN-UHFFFAOYSA-N checkY
  (verify)

Pheniramine (Avil) is an antihistamine with anticholinergic properties used to treat allergic conditions such as hay fever or urticaria. It has relatively strong sedative effects, and may sometimes be used off-label as an over-the-counter sleeping pill in a similar manner to other sedating antihistamines such as diphenhydramine.

Pheniramine is generally sold in combination with other medications, rather than as a stand-alone drug, although some formulations are available containing pheniramine by itself. As an example, Neo Citran contains pheniramine.

Chemical relatives

Derivatives of pheniramine include chlorpheniramine, dexchlorpheniramine, dexbrompheniramine, deschlorpheniramine, triprolidine, and brompheniramine. Two other halogenated derivatives, iodopheniramine and fluorpheniramine, are currently in use for research on combination therapies for malaria and some cancers. The halogenation of pheniramine increases its potency by 20-fold.

Side effects

Avil may cause drowsiness, and over-dosage may lead to sleep disorders. Overdose may lead to seizures, especially in combination with alcohol. Those with cartisol for long term should avoid avil as it may cause loss of adreline which may lead to losing consciousness.

References