Bulgarian Experience with Adverse Drug Reaction Reports from Patients and Consumers – Retrospective Data-base Study

Background: Since 2012, in compliance with the changes in the European legislation, the Bulgarian Drug Agency (BDA) has been receiving adverse drug reaction (ADR) reports directly from patients as well as from healthcare professionals and marketing authorization holders (MAH). Adverse reaction repor...

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Autors principals: Getova Violeta I., Georgiev Stanislav R., Stoimenova Assena H., Petkova-Georgieva Elina S.
Format: Article
Idioma:English
Publicat: Pensoft Publishers 2018-09-01
Col·lecció:Folia Medica
Matèries:
Accés en línia:http://www.degruyter.com/view/j/folmed.2018.60.issue-3/folmed-2018-0016/folmed-2018-0016.xml?format=INT