Position and Processing of Adverse Drug Reactions Directly Submitted by Patients to National Regulatory Authorities in Europe
نویسندگان
چکیده
منابع مشابه
Discrepancies in listed adverse drug reactions in pharmaceutical product information supplied by the regulatory authorities in Denmark and the USA
Pharmaceutical product information (PI) supplied by the regulatory authorities serves as a source of information on safe and effective use of drugs. The objectives of this study were to qualitatively and quantitatively compare PIs for selected drugs marketed in both Denmark and the USA with respect to consistency and discrepancy of listed adverse drug reaction (ADR) information. We compared ind...
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Objective: One of the most common causes of death is the adverse drug reactions. The volume and dispersion of information is one of the problems of information systems for registering unwanted adverse drug reactions. This study aims to design a National Minimum Dataset (NMDS) for reporting the unwanted adverse drug reactions. Methods: This descriptive-comparative study was conducted in Mashhad...
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School of Marilia, São Paulo, Brazil; Flow Citometry, and; Dermatology, Medical School of Marilia, Marilia, Brazil. Background: The prevalence of hypersensitivity to nonsteroidal anti-inflammatory drugs (NSAIDs) is high and its in vitro diagnostic is a challenge. The basophil activation test with determination by flow cytometry (FC), of the expression rate of CD63 molecules has been much studie...
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ژورنال
عنوان ژورنال: Journal of Pharmacovigilance
سال: 2014
ISSN: 2329-6887
DOI: 10.4172/2329-6887.1000122