Commentary on "secondary use of electronic health record data: Spontaneous triggered adverse drug event reporting" by linder et al.
Summary of "Commentary on "secondary use of electronic health record data: Spontaneous triggered adverse drug event reporting" by linder et al."
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US Food and Drug Administration, Silver Spring, MD, USA.
This article was published in the following journal.
Name: Pharmacoepidemiology and drug safety
Medical and Biotech [MESH] Definitions
Systematic gathering of data for a particular purpose from various sources, including questionnaires, interviews, observation, existing records, and electronic devices. The process is usually preliminary to statistical analysis of the data.
Medical Record Administrators
Individuals professionally qualified in the management of patients' records. Duties may include planning, designing, and managing systems for patient administrative and clinical data, as well as patient medical records. The concept includes medical record technicians.
The use of electronic equipment to observe or record physiologic processes while the patient undergoes normal daily activities.
Detailed account or statement or formal record of data resulting from empirical inquiry.
National Practitioner Data Bank
A databank established by the Health Care Quality Improvement Act of 1986 authorizing the Department of Health and Human Services to collect and release information on the professional competence and conduct of physicians, dentists, nurses, and other health care practitioners. The data include adverse actions on physicians' malpractice, licensure, hospital privileges, concealing of pertinent information, and the like.
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