Merck
CN

FDA-approved drug labeling for the study of drug-induced liver injury.

Drug discovery today (2011-06-01)
Minjun Chen, Vikrant Vijay, Qiang Shi, Zhichao Liu, Hong Fang, Weida Tong
摘要

Drug-induced liver injury (DILI) is a leading cause of drugs failing during clinical trials and being withdrawn from the market. Comparative analysis of drugs based on their DILI potential is an effective approach to discover key DILI mechanisms and risk factors. However, assessing the DILI potential of a drug is a challenge with no existing consensus methods. We proposed a systematic classification scheme using FDA-approved drug labeling to assess the DILI potential of drugs, which yielded a benchmark dataset with 287 drugs representing a wide range of therapeutic categories and daily dosage amounts. The method is transparent and reproducible with a potential to serve as a common practice to study the DILI of marketed drugs for supporting drug discovery and biomarker development.

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泰莫西芬, ≥99%
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地塞米松, powder, BioReagent, suitable for cell culture, ≥97%
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D -甘露醇, ≥98% (GC)
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烟酸, ≥98%
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利福平, ≥95% (HPLC), powder or crystals
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乙醇胺, ≥98%
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乙醇胺, ACS reagent, ≥99.0%
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β-雌二醇, ≥98%
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烟酸, ≥99.5% (HPLC)
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D -甘露醇, ACS reagent
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叶酸, ≥97%
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羟基脲, 98%, powder
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3,3′,5-三碘代-L-甲状腺原氨酸, ≥95% (HPLC), powder
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吲哚美辛, 98.5-100.5% (in accordance with EP)
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