Zobrazeno 1 - 10
of 45
pro vyhledávání: '"D P Benziger"'
Publikováno v:
Clinical nephrology. 75(1)
The purpose of this study was to characterize the pharmacokinetics and tolerability of daptomycin in subjects undergoing hemodialysis (HD) or continuous ambulatory peritoneal dialysis (CAPD).16 noninfected adults on stable dialysis regimens were enro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5ad7061cf58ec206a68a932554dfab6c
https://pubmed.ncbi.nlm.nih.gov/21176752
https://pubmed.ncbi.nlm.nih.gov/21176752
Autor:
D E, Katz, K C, Lindfield, J N, Steenbergen, D P, Benziger, K J, Blackerby, A G, Knapp, W J, Martone
Publikováno v:
International journal of clinical practice. 62(9)
Methicillin-susceptible and -resistant (MRSA) Staphylococcus aureus are significant causes of complicated skin and skin structure infections (cSSSI). The bactericidal antibiotic daptomycin is approved for gram-positive cSSSI at 4 mg/kg/day for 7-14 d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9ce4ccf8bdd9b5ecb874633785ddcfe5
https://pubmed.ncbi.nlm.nih.gov/18793374
https://pubmed.ncbi.nlm.nih.gov/18793374
Autor:
Paul J. Fielder, Andrew R. Hoffman, Le Dao, David M. Cook, J. D. Reimann, D. P. Benziger, Kathleen Ford, Beverly M. K. Biller, A. Illeperuma, Kenneth M. Attie, Mary Lee Vance, Lawrence S. Phillips, Sandra L. Blethen
Publikováno v:
The Journal of clinical endocrinology and metabolism. 87(10)
Long-term GH replacement therapy is indicated for children with growth failure due to GH deficiency (GHD). We evaluated the feasibility of administering a long-acting GH preparation [Nutropin Depot (somatropin, rDNA origin) for injectable suspension]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::574cc213c618bcaf21a977deb5d2ae30
https://pubmed.ncbi.nlm.nih.gov/12364427
https://pubmed.ncbi.nlm.nih.gov/12364427
Autor:
D P Benziger, J A Johnson
Publikováno v:
Antimicrobial Agents and Chemotherapy. 27:774-781
Sprague-Dawley rats received [14C]amifloxacin mesylate either orally or intravenously at 20 mg (base equivalent) per kg. Blood radioactivity peaked at 0.5 h after oral administration and was equivalent to 7.54 micrograms/ml for males and 6.73 microgr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2663c1a4a9e4e4b55ab78bd6dde45dfa
https://doi.org/10.1128/aac.27.5.774
https://doi.org/10.1128/aac.27.5.774
Autor:
D P Benziger, J Edelson
Publikováno v:
Antimicrobial Agents and Chemotherapy. 22:475-481
[14C]arildone was administered both topically and intravaginally to mice 5 times a day for 7 days to simulate conditions of clinical usage. Urinary and fecal excretion of radioactivity indicated that arildone was extensively absorbed by both routes o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aba7221eb5b28bbf49aad33dd789e0e2
https://doi.org/10.1128/aac.22.3.475
https://doi.org/10.1128/aac.22.3.475
Publikováno v:
Archives internationales de pharmacodynamie et de therapie. 258(1)
The disposition of quinfamide 1-(dichloroacetyl)-6-(2-furoyloxy)-1, 2, 3, 4-tetrahydroquinoline, an enteric anti-amoebic agent, was studied in the rat. A peak blood level equivalent to 2.3 micrograms/ml of quinfamide was observed at 7 hr following a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b8b2c2d6d193b94ae5c34e14f262f78c
https://pubmed.ncbi.nlm.nih.gov/7138144
https://pubmed.ncbi.nlm.nih.gov/7138144
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 5(3)
Radioactivity from orally administered single doses of cyclindole-14C was excreted primarily in the urine of the rat (99%/48 hr), monkey (80%/120 hr), and dog (70%/144 hr). Approximately 38-58% of a daily dose of cyclindole was recovered from 24-hr h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::05187e56cce6ec71e229dc98e8bf27f0
https://pubmed.ncbi.nlm.nih.gov/17521
https://pubmed.ncbi.nlm.nih.gov/17521
Publikováno v:
Clinical pharmacology and therapeutics. 40(6)
Ten healthy male subjects were phenotyped with isoniazid for their acetylator status and then received intravenous amrinone at a dose of 75 mg during a period of 10 minutes. Blood samples were drawn at specified times during a 24-hour period after do
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3991789ad2465506f0bd31f931c552ef
https://pubmed.ncbi.nlm.nih.gov/3780123
https://pubmed.ncbi.nlm.nih.gov/3780123
Publikováno v:
The Journal of infectious diseases. 154(4)
liver, serum (ng/ml), and muscle, respectively at 0.5-1.0 hr after medication. The picornaviruses, a group of small, single-stranded RNA viruses, are the causative agents of several disease states. Among the picornaviridae are two groups that cause d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4273a8174386809571d289d023e71ba7
https://pubmed.ncbi.nlm.nih.gov/3745975
https://pubmed.ncbi.nlm.nih.gov/3745975
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 9(6)
Peak levels of radioactivity in blood occurred 1.0 hr after oral administration of 3H-sulfinalol hydrochloride to rats, dogs, and monkeys. The plasma decay curve for intact sulfinalol in the dog was biphasic, with apparent first-order half-lives of 0
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7546e28d577244428c02febb83d2ebcb
https://pubmed.ncbi.nlm.nih.gov/6120804
https://pubmed.ncbi.nlm.nih.gov/6120804