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Altiva (Fexofenadine)
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Fexofenadine

Altiva is a hydrochloride salt form of Altiva, a carboxylated metabolic derivative of terfenadine and third generation selective histamine H1-receptor antagonist with antihistaminic and non-sedative effects. Altiva 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.

Other names for this medication:
Fexofenadine, Aerodan, Allerfex, Allerstat, Altiva, Axodin, Drusa, Feksine, Fenadex, Fenadin, Fenax, Fenixa, Fexidine, Fexo, Fexodine, Fexofast, Fexofen, Fexofenadin, Fexofenadina, Fexotabs, Histafree, Histaloc, Nefoxef, Rinolast, Telfast, Telfexo, Xergic,

Similar Products:
Almac, Fenax, Ledion, Lenar, Neptor, Rispone, Cyclomed, Ataraxone, Clindacin, Wymox, Eusaprim, Tolep, Mopral, Endoxan, Finpecia, Benicar, Euradal, Lequin, Duprost, Talavir, Topzole, Harnalidge, Tersen, Torva, Trimesulfin, Zoton, Antirobe, Lanex, Klindan, Ibuprofen, Normatens, Piramil,

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Cell division and differentiation in avian embryos: techniques for study of early neurogenesis and myogenesis. Despite the advances in our understanding of aging-associated behavioral decline, relatively little is known about how aging affects neural circuits that regulate specific behaviors, particularly the expression of genes in specific neural circuits during aging. Parallel first-order and Michaelis-Menten elimination kinetics of ethanol.

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6-keto-prostaglandin F1 alpha (6-keto-PGF1 alpha), thromboxane B2(TXB2)content, plasminogen activator (PA), plasminogen activator inhibitor (PAI) activity in cultured medium and cyclic adenosine monophosphate (cAMP) level in EC were measured with radioimmunoassay (RIA), chromogenic substrates methods, in order to assess the effect and mechanism of captopril (CP) on antithrombus function of EC. This is achieved, in part, through the opposing cytokines produced by T helper 1 (Th1) and Th2 cells. Problematic use of alcohol, tobacco, and other drugs, including prescription medications, contributes to increased risk for injury, illness, suffering, and premature death across the lifespan. Compared with the DMSO treatment, propofol produced a significant inhibition of WDR neuronal activity evoked by both noxious heat (45, 47, 49 or 53 degrees C, 15 s) and mechanical (pinch, 10 s) stimuli applied to their cutaneous receptive fields (cRF) on the ipsilateral hind paw skin.

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Synthesis of BILN 2061, an HCV NS3 protease inhibitor with proven antiviral effect in humans. Our experience with a variety of surgical procedures for venous obstruction is described. This paper describes a novel, combined isolation of a cysteine proteinase (called trypanopain-Tb) and a serine oligopeptidase (which we call oligopeptidase-Tb) from Trypanosoma brucei brucei, as well as a comparison of the activities of these two enzymes against several host regulatory molecules. This may be of importance for host-parasite relationship and immune response. We report a patient with discoid lupus erythematosus (DLE) and associated allergic contact dermatitis (ACD) in the eyelids.

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NFATc1 activates the acetylcholinesterase promoter in rat muscle. Over the last decade, cytomegalovirus (CMV) has been suggested to promote the development of glioblastoma multiforme (GBM). Metabolic disturbances often present in pregnancy complicated by insulin-dependent diabetes mellitus may have important effect on birthweight. Identification of a novel vga(E) gene variant that confers resistance to pleuromutilins, lincosamides and streptogramin A antibiotics in staphylococci of porcine origin. The inverses of the variances of the genotype-by-environment BLUPs were used as weights.

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