[The hydrochloride salt form of fexofenadine, a carboxylated metabolic derivative of terfenadine and third generation selective histamine H1-receptor antagonist with antihistaminic and non-sedative effects. Fexofenadine competitively binds peripheral H1-receptors, thereby stabilizing an inactive conformation of the receptor. Consequently histamine binding and activity as a result of mast-cell degranulation followed by the release of multiple inflammatory mediators, such as interleukins, prostaglandin and leukotriene precursors, is blocked, thereby preventing the triggering of pro-inflammatory pathways. ( NCI )]
UMLS (NCI) C0771752Fexofenadine Hydrochloride
FEXOFENADINE HYDROCHLORIDE PREPARATION
- Organic Chemical
- Pharmacologic Substance
Relation/PAR: FEXOFENADINE
Relation/CHD: FEXOFENADINE HYDROCHLORIDE 60 MG
FEXOFENADINE HYDROCHLORIDE 180 MG
FEXOFENADINE HYDROCHLORIDE 30 MG