Giving Information on Medicinal Products to the General Public: In Search of a Definition to Safeguard the Patient

Andrea Faeh

1 Citationer (Scopus)

Abstract

Information on medicinal products is vital for enabling patients to give informed consent to the use of a specific product. Within the European Union (EU) the debate about how much information about prescription-only medicinal products should be made available to patients has gone on for the past five years with no definite conclusion yet. This contribution assesses the current legislation and the ongoing debate in order to identify the challenges and the prospect of new legislation, and consider its potential implications for the scope for advertising and for patient safety.

OriginalsprogEngelsk
TidsskriftEuropean Journal of Health Law
Vol/bind21
Udgave nummer2
Sider (fra-til)176-195
Antal sider20
ISSN0929-0273
DOI
StatusUdgivet - 2014

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