Abstract

Side effects are more frequent and severe, or simply appear by just talking about them. But not the informed consent is to be challenged, rather the form of giving risk information. Nocebo effects mainly originate from induced negative expectations, not from the information itself. Concerns about legal consequences of an incomplete list of risks do not release from the responsibility to guide and help the patient to an understanding and a balanced decision.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.