Titlebook: Clinical Nephrotoxins; Renal Injury from Dr M. E. Broe,G. A. Porter,G. A. Verpooten Book 19981st edition Springer Science+Business Media Do

TOXIN

Terminal

critique

Max Dirndorfer,Herbert Fischer,Stephan Sneedtial reports [1–4], observing that phenacetin was present in most abused analgesics, held this substance solely responsible for the development of what was called “phenacetin nephritis”. In the late 1970’s, it became apparent that the abuse of different kinds of analgesic mixtures induced severe ren

Frenetic

Herbert Fischer,Josef Schneebergerhis is in view of the heterogeneity of the populations who consume these agents and the variability in social customs that importantly influence the per capita ingestion of analgesic-anti-inflammatory drugs. Nonetheless, in most general populations, as encountered by family physicians in the develop

凹槽

跳動(dòng)

judiciousness

Business Process Modeling ,izeddividualized care preferred nowadays. This phenomenon was largely due to the recent development of new classes of antihypertensives, which made it possible to adequately lower blood pressure in most patients with only one or two antihypertensive drugs, thus avoiding the need for a combination of mul

個(gè)人長(zhǎng)篇演說(shuō)

浮雕

Albert Fleischmann,Stefan Ra?,Robert SingerPharmacology and clinical pharmacology define the desirable and undesirable effects of drugs and xenobiotics whereas pharmacokinetics defines the various processes that are involved in absorption — distribution — elimination of these agents. Needless to say that the former may strongly influence the latter.

groggy

Andreas Hufgard,Eduard GerhardtThere are two main types of analgesic related renal injury: “(1) classical analgesic nephropathy, and (2) non-steroidal anti-inflammatory drug renal toxicity.” Recently, the association of a chronic interstitial nephritis with the use of 5-aminosalicylic acid in patients with inflammatory bowel disease has been documented by several case reports.