UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
F F F- F0 FA FB FC FD FE FF FG FH FI FJ FK FL FM FN FO FP FR FS FT FU FX FY
FE2 FE5 FEA FEB FEC FED FEE FEI FEL FEM FEN FEP FER FES FET FEV FEW FEX

Fexofenadine HCl

[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) C0771752
Fexofenadine 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

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