Zobrazeno 1 - 10
of 140
pro vyhledávání: '"G S, AVERY"'
Publikováno v:
American journal of botany. 33(7)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::98077adcbba785827f62ec1ad65b4aa7
https://pubmed.ncbi.nlm.nih.gov/20280150
https://pubmed.ncbi.nlm.nih.gov/20280150
Publikováno v:
Drugs. 7:337-343
Fluocinonide (fluocinolone acetonide acetate) 0.05 % in FAPG base2 is a new fluorinated topical corticosteroid incorporated into a specially formulated non-aqueous synthetic base for use in psoriasis, eczema and other inflammatory dermatoses. In doub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c0c87c298a9790e33f27cd005075e86
https://doi.org/10.2165/00003495-197407050-00004
https://doi.org/10.2165/00003495-197407050-00004
Publikováno v:
Drugs. 22:423-460
Synopsis: Cefoperazone1 new ‘third generation’ semisynthetic injectable cephalosporin. It has a broad spectrum of antibacterial activity which includes Pseudomonas aeruginosa (unlike older cephalosporins), along with the Enterobacteriaceae and ot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08f7478349a69f604e1acf79a7dfcb16
https://doi.org/10.2165/00003495-198122060-00002
https://doi.org/10.2165/00003495-198122060-00002
Publikováno v:
Drugs. 14:163-197
Synopsis: Prazosin1 is a peripheral vasodilator antihypertensive agent derived from quinazoline. Animal studies suggest that its hypotensive effect results from relaxation of peripheral arterioles as a consequence of blockade of post-synaptic α-adre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea9b84299e4143e30cac5e59ea7674dd
https://doi.org/10.2165/00003495-197714030-00002
https://doi.org/10.2165/00003495-197714030-00002
Publikováno v:
Drugs. 19:161-180
Colestipol1 is an anion exchange resin with bile acid sequestering properties resembling those of cholestyramine, another lipid-lowering binding resin. In daily doses of 15 to 30g colestipol reduces total plasma cholesterol concentrations (primarily
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31e3143e8dd5b8ca826cd38bf395b623
https://doi.org/10.2165/00003495-198019030-00001
https://doi.org/10.2165/00003495-198019030-00001
Publikováno v:
Drugs. 27:210-231
Oxatomide is an orally active H1-histamine receptor antagonist which, as appears to occur with some other antihistamines, also inhibits mast cell degranulation. Oxatomide has demonstrated response rates similar to those with other more established me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::800340560f292b490fef5d6d7e85c322
https://doi.org/10.2165/00003495-198427030-00003
https://doi.org/10.2165/00003495-198427030-00003
Publikováno v:
Drugs. 17:1-37
Cefoxitin is a beta-lactam antibiotic derived from cephamycin C, a naturally occurring substance produced by Streptomyces lactamdurans. Its resistance to destruction by beta-lactamases results in a broad spectrum of antibacterial activity which inclu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aeee04fca22d4c1628e5c77ac1f52c52
https://doi.org/10.2165/00003495-197917010-00001
https://doi.org/10.2165/00003495-197917010-00001
Publikováno v:
Drugs. 7:283-296
Therapeutic trials of intranasal sodium cromoglycate have shown it to be of value in some patients with seasonal or perennial allergic rhinitis and in some with perennial rhinitis of unknown cause. Its use usually enables a reduction in antihistamine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc845b3a5b378f8b861f787ec7f780b5
https://doi.org/10.2165/00003495-197407030-00003
https://doi.org/10.2165/00003495-197407030-00003
Autor:
G. S. Avery
Publikováno v:
Drugs. 14:132-146
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf872f98a66673f014c2d9a79ae4b233
https://doi.org/10.2165/00003495-197714020-00006
https://doi.org/10.2165/00003495-197714020-00006
Publikováno v:
Drugs. 24:267-303
Ranitidine is a new histamine H2-receptor antagonist which, unlike cimetidine, does not contain an imidazole group. On a weight basis, ranitidine is 4 to 10 times more potent than cimetidine in inhibiting stimulated gastric acid secretion in humans.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ecc639880259aa0526682bb1f6c4371
https://doi.org/10.2165/00003495-198224040-00002
https://doi.org/10.2165/00003495-198224040-00002