Zobrazeno 1 - 9
of 9
pro vyhledávání: '"L J, Lees"'
Publikováno v:
European Journal of Clinical Microbiology. 2:340-344
Eight volunteers each received lg of probenecid followed immediately by 1.5 g sultamicillin, both given by the oral route. Plasma concentrations of ampicillin and sulbactam were measured using a differential bioassay method. An ampicillin mean peak p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21bacb6336a172bd9409ed8b0265aeb7
https://doi.org/10.1007/bf02019464
https://doi.org/10.1007/bf02019464
Publikováno v:
British Journal of Clinical Pharmacology. 27:851-859
1. Azole antifungal agents such as ketoconazole act by inhibiting cytochrome P-450 mediated sterol synthesis in the fungal cell membrane and thus have the potential to interfere with mammalian steroidogenesis. Fluconazole is a novel orally-effective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d286bea33d86eded5f07fd8c396d536
https://doi.org/10.1111/j.1365-2125.1989.tb03449.x
https://doi.org/10.1111/j.1365-2125.1989.tb03449.x
Publikováno v:
British Journal of Clinical Pharmacology. 14:213-217
1 Plasma and biliary concentrations of amoxycillin and ceftriaxone were measured after bolus intravenous administration (500 mg) in four subjects with normal hepato-biliary and renal function. 2 The mean plasma elimination half-life for ceftriaxone (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6444925ed4861e640366a9dd3c835293
https://doi.org/10.1111/j.1365-2125.1982.tb01964.x
https://doi.org/10.1111/j.1365-2125.1982.tb01964.x
Publikováno v:
Journal of Infectious Diseases. 137:82-86
A double-stranded RNA of fungal origin (BRL 5907) was given intranasally to volunteers. Apart from mild local irritancy of the higher dosage, the compound was well tolerated. A double-blind placebo-controlled trial of a three-day course (5 mg per day
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b23ed0fdf613e0c06ddc93f2ac94173
https://doi.org/10.1093/infdis/137.1.82
https://doi.org/10.1093/infdis/137.1.82
Autor:
L J, Lees, J W, Harding
Publikováno v:
The British journal of clinical practice. 28(10)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4219256d42052330de5e8216f31368a9
https://pubmed.ncbi.nlm.nih.gov/4613369
https://pubmed.ncbi.nlm.nih.gov/4613369
Publikováno v:
Chemotherapy. 24(4)
Talampicillin is an ester of ampicillin which is readily hydrolysed on absorption to release ampicillin. It is well absorbed from the gastro-intestinal tract resulting in a greater bioavailiability of ampicillin than can be achieved with equivalent d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8df8fd8fd0e067198db702ab413cee1
https://pubmed.ncbi.nlm.nih.gov/348415
https://pubmed.ncbi.nlm.nih.gov/348415
Publikováno v:
Antimicrobial agents and chemotherapy. 17(6)
Alafosfalin is a phosphonodipeptide with significant activity as an antibacterial agent and as a potentiator of beta-lactam antibiotics. Studies in humans showed that oral doses of 50 to 2,500 mg were well absorbed, but some metabolic hydrolysis occu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::226ba8e98e5205ad333a722eb853347a
https://pubmed.ncbi.nlm.nih.gov/7406481
https://pubmed.ncbi.nlm.nih.gov/7406481
Autor:
L J, Lees
Publikováno v:
The British journal of clinical practice. 28(10)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3ac5d52a24f0ccb1e54850bb9ab0a350
https://pubmed.ncbi.nlm.nih.gov/4613367
https://pubmed.ncbi.nlm.nih.gov/4613367
Autor:
J W, Harding, L J, Lees
Publikováno v:
The Practitioner. 209(251)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6730fd6cfe3da6a435a5b81e9b93bc33
https://pubmed.ncbi.nlm.nih.gov/4562945
https://pubmed.ncbi.nlm.nih.gov/4562945