Open Access Articles- Top Results for Pheniramine


Systematic (IUPAC) name
Clinical data
AHFS/ International Drug Names
MedlinePlus a606008
  • AU: A
  • US: C (Risk not ruled out)
Oral ; injection (intramuscular or slow intravenous); topical (ophthalmic/nasal solution)
Pharmacokinetic data
Metabolism Hepatic hydroxylation, demethylation and glucuronidation
Excretion Renal
86-21-5 7pxY
D04AA16 R06AB05
PubChem CID 4761
DrugBank DB01620 7pxY
ChemSpider 4597 7pxY
UNII 134FM9ZZ6M 7pxY
KEGG D08355 7pxY
Chemical data
Formula C16H20N2
240.343 g/mol
 14pxY (what is this?)  (verify)

Pheniramine (INN, trade name Avil, among others) 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 also commonly found in eyedrops used for the treatment of allergic conjunctivitis.

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 chlorphenamine, 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

Pheniramine may cause drowsiness, bradycardia and over-dosage may lead to sleep disorders. Overdose may lead to seizures, especially in combination with alcohol. People combining with cortisol in the long term should avoid pheniramine as it may cause lowered levels of adrenaline (epinephrine) which may lead to loss of consciousness.

See also


External links

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