对乙酰氨基酚
上市后监督
医学
他达拉非
不利影响
风险分析(工程)
药理学
毒理
外科
生物
勃起功能障碍
作者
K. Blum,W. Anthony Hawkins,Tanja Bernier,Claudia Sehner,Eva Zeller,Markus Schwind,Thomas D. Pfister,Martín Kohan,Osahon Osadolor,Milica Glogovac,Gregor Tuschl,David G. Dolan,Ester Lovšin Barle
标识
DOI:10.1016/j.yrtph.2020.104692
摘要
In the pharmaceutical industry, cleaning criteria are required for multipurpose manufacturing facilities. These Health Based Exposure Limits (HBELs), also called permitted daily exposures (PDEs) values, are derived from toxicological and pharmacological evaluation of the active pharmaceutical ingredients (APIs). The purpose of this publication is to show an example of how authors from different companies evaluate a generic drug, paracetamol, and discuss different approaches and relevance of the nonclinical studies for deriving PDEs. PDE limits of 25 mg/day for the oral route, and 20 mg/day for the intravenous (i.v.) and inhalation (inhal.) routes, respectively, were established herein. However, it has been already recognised that there are acceptable differences in the PDE calculations, which may be based on data accessibility, company-specific science-policy decisions or expert judgments. These differences can cause up to a 3-fold lower or higher values. If unnecessarily high factors are applied, this would result in a very conservative PDE value and unneeded additional cleaning and higher manufacturing costs. The PDE values presented are considered to be protective against adverse and pharmacological effects observed in clinical trials and in this case, a very long postmarketing period of paracetamol.
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