نتایج جستجو برای: drug safety evaluation
تعداد نتایج: 1576394 فیلتر نتایج به سال:
BACKGROUND The promotion of patient safety and drug safety through promotion of pharmacist's drug safety practice was among the most important aims of China's health delivery system reform, but regional inequity in pharmacist's drug safety practice was still serious in China. METHODS The 2011 national patient safety and medication error baseline survey was carried out for the first time in Ch...
Addressing safety concerns such as drug-induced kidney injury (DIKI) early in the drug pharmaceutical development process ensures both patient safety and efficient clinical development. We describe a unique adjunct to standard safety assessment wherein the metabolite profile of treated animals is compared with the MetaMap Tox metabolomics database in order to predict the potential for a wide va...
Literature reports of suspected adverse drug reactions (ADRs) associated with medicinal products for human use are not just an integral part of signal detection activities, but are also an important source of information for professionals involved in patient management. Therefore, it is with great pleasure that Adis (Springer) announces the launch of Drug Safety Case Reports, a new peerreviewed...
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Drug safety monitoring is important in children. Young age, polypharmacy, prolonged hospitaliza-tion, being critically ill and use of unlicensed and off-label drugs have been identified as risk factors which predispose a child to experience an adverse drug reaction. In our country, the HIV/AIDS epidemic, setting up of intensive care units, increasing availability of imaging studies, and the int...
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Amendment s the FEMA Expert Panel enters its fifth decade, it continues to conduct a comprehensive program of safety evaluation of flavoring substances under the authority of Section 201(s) of the Federal Food, Drug, and Cosmetic Act, a provision commonly known as the GRAS (“generally recognized as safe”) provision. Expert Panel activities primarily involve the evaluation of new flavoring subst...
Concern over the presence of veterinary drug residues in food has been increasing world wide. Because of this concern the Food and Drug Administration's Center for Veterinary Medicine (CVM) has been involved on an international basis in efforts to develop food safety standards for veterinary drugs. The major thrust of the Codex Committee on Residues of Veterinary Drugs in Foods (CC/RVDF) has be...
This review summarizes gender differences (GDs) in drug response. Although GDs have been described both in pharmacodynamics and pharmacokinetics, their role in clinical practice is not yet completely elucidated. The evidence that women have been less enrolled in clinical trials and that a gender-specific analysis usually is not included in the evaluation of results, contributes largely to this ...
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