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Titlebook: Drug Allergy; Clinical Aspects, Di Brian A. Baldo,Nghia H. Pham Book 2021Latest edition Springer Nature Switzerland AG 2021 drug allergies.

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發(fā)表于 2025-3-25 06:10:33 | 只看該作者
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發(fā)表于 2025-3-25 10:12:28 | 只看該作者
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發(fā)表于 2025-3-25 13:39:15 | 只看該作者
Scope of this Book: Adverse Reactions to Drugs and Drug Allergy,esignated type B reactions, are made up of immune-mediated and non-immune sensitivities. The former group includes hypersensitivity responses, while the non-immune reactions are divided into so-called pseudoallergies, idiosyncratic reactions, and intolerances. Reactions designated as type A are pred
24#
發(fā)表于 2025-3-25 19:31:34 | 只看該作者
Classification and Descriptions of Allergic Reactions to Drugs, and the allergic signs and symptoms are triggered by cross-linking of mast cell-bound IgE which leads to mast cell degranulation and release of inflammatory mediators. Drugs well-known to cause type I reactions include β-lactams, neuromuscular blockers, and some NSAIDs. Anaphylactoid reactions may
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發(fā)表于 2025-3-25 22:10:19 | 只看該作者
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28#
發(fā)表于 2025-3-26 10:28:59 | 只看該作者
Other Antimicrobial Drugs, most commonly occurring adverse effect caused by vancomycin is red man syndrome. Immediate allergic reactions to the structurally related teicoplanin are being increasingly reported. Neomycin consistently ranks in the top 10% of the most common causes of allergic contact dermatitis, while the incid
29#
發(fā)表于 2025-3-26 14:33:48 | 只看該作者
Drugs and Other Agents Used in Anesthesia and Surgery,f reactions and an incidence of 1 in 1000 to 20,000. In some recent surveys, antibiotics appear to have replaced NMBDs as the prime offender. Reactions to NMBDs are mediated by IgE antibodies with specificity for tertiary and quaternary ammonium ions, but adjoining structures may also be recognized.
30#
發(fā)表于 2025-3-26 17:10:55 | 只看該作者
Opioid Analgesic Drugs,lief. These drugs show common structural features, bind specifically to opioid receptors, and possess morphine-like pharmacological action. Tramadol and tapentadol differ from other opioid analgesics in their monoaminergic activities as well as their weak affinity for the μ opioid receptor. Meperidi
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