JUST
发表于 2025-3-30 11:28:06
http://reply.papertrans.cn/43/4241/424071/424071_51.png
Choreography
发表于 2025-3-30 15:28:19
Ben Rogersclopidogrel, and prasugrel; and platelet glycoprotein IIb/IIIa receptor antagonists such as abciximab, tirofiban, and eptifibatide are reviewed in this chapter. Aspirin is more commonly associated with cutaneous reactions due to its use as a nonsteroidal antiinflammatory drug.
掺和
发表于 2025-3-30 17:54:55
James H. Fetzereported one to cause adverse cutaneous reactions. Amiodarone is a lipid soluble agent which accumulates in peripheral tissues including the adipose tissue, and the skin is one of the excretion ways of the drug. It has a very long half-life, up to 6 months, so it is stated that toxic side effects may
Conserve
发表于 2025-3-30 23:37:31
Clark Glymouramil, gallopamil), dihydropyridines (nifedipine, nicardipine, nisoldipine, nimodipine, nitradipine, nilvadipine, nitrendipine, benidipine, felodipine, amlodipine, barnidipine, cilnidipine, efonidipine, manidipine, lacidipine, isradipine, lercanidipine, aranidipine, azelnidipine, pranidipine, clevidi
Nebulous
发表于 2025-3-31 02:25:53
http://reply.papertrans.cn/43/4241/424071/424071_55.png
灯泡
发表于 2025-3-31 06:57:36
http://reply.papertrans.cn/43/4241/424071/424071_56.png
RAG
发表于 2025-3-31 11:41:24
J. Alberto Coffaions because they are the most difficult to deal with. It starts with a general description of the major targets for ADRs followed by a description of what are presently believed to be mediators and biochemical pathways involved in idiosyncratic drug reactions. There is also a description of several
狂热语言
发表于 2025-3-31 16:47:57
http://reply.papertrans.cn/43/4241/424071/424071_58.png
繁殖
发表于 2025-3-31 19:00:53
http://reply.papertrans.cn/43/4241/424071/424071_59.png
pericardium
发表于 2025-3-31 23:50:42
O. Costa de Beauregardctions can be categorized into a number of sites that include the cell membrane-bound receptors, the second messenger system, ionic channels, ionic pumps, and intracellular organelles. Additionally, interference with the neuronal input to the heart can also present a global site where adverse drug e