
- Disposal method: SRP:最有利的行动方案是使用具有较低职业暴露或环境污染内在倾向的替代化学品产品。回收任何未使用材料的部分以获得批准的用途,或将其返回给制造商或供应商。化学品的最终处置必须考虑:材料对空气质量的影响;在土壤或水中的潜在迁移;对动物、水生和植物生命的影响;以及符合环境和公共卫生法规。
- Regulatory information: 新西兰EPA化学品清单状态:2(5H)-呋喃酮,4-4-(甲基磺酰基)苯基-3-苯基-:没有单独批准,但可在适当的团体标准下使用
- Hepatotoxicity: 可能性评分:C(可能是引起明显肝损伤的罕见原因)。
- Special Reports: Ahuja N 等人;罗非昔布:关于理化性质、药物制剂、药效学和药代动力学方面的更新;J Pharm Pharmacol 55 (7): 859-94 (2003)
- Human toxicity extract: /病例报告/ 血管性水肿是罗非昔布(一种环氧化酶-2(COX-2)抑制剂)的公认副作用。但尚未记录到因服用该药后出血性肺水肿导致的死亡。本文报告了一名60岁男性的病例,他在服用两次12.5mg罗非昔布后,出现血管性水肿和出血性肺水肿而死亡。
- Hazard categories and classifications: 急性毒性 4级 (100%)
- Non-human toxic extract: /实验室动物:发育或生殖毒性/罗非昔布在大鼠和兔子中分别以口服剂量≥10和≥75 mg/kg/天时,导致着床前和着床后损失以及降低胚胎/胎儿存活率。这些变化是由于抑制前列腺素合成所致,并非女性生殖功能永久性改变的结果。在≥5 mg/kg/天剂量下,大鼠产后幼崽死亡率增加。在给予罗非昔布单剂量的怀孕大鼠研究中,所有使用剂量均观察到与治疗相关的动脉导管直径减小。与其他已知抑制前列腺素合成的药物类似。
- Antidote and first aid: 在过量情况下,从胃肠道中移除未吸收的药物,监测患者,并根据需要提供支持治疗。血液透析不会将其移除。
- Drug Induced Liver Injury: 参考文献:DOI:10.1016/j.drudis.2019.09.022
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Research chemical ≥98. 0%; 100mg
Research chemical ≥98. 0%; 100mg; supplied for laboratory research, analysis, inspection, and scientific procurement use; specifications: ≥98. 0%; 100mg.




