Adverse event log template
[DOC File]ADVERSE EVENT LOG - UNC Research
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Mar 13, 2019 · ADVERSE EVENT. Make a separate entry for: All new adverse events. All AEs with increased severity. All AEs with changes in study drug relationship. All medical conditions present at study drug initiation which have worsened ( if AE meets definition of serious* Grade / Intensity. Asymptomatic. Mild Moderate. Severe Start Date End Date
[DOCX File]qualitycompliance.research.utah.edu
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ADVERSE EVENT LOG. Study: _____ Participant. ID: Participant. Initials: _____ _____ _____ IRB. Number: _____ PI
[DOC File]Has the subject experienced any adverse events
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Adverse Event Log. Has the subject experienced any adverse events? YES NO (Complete at End of Study) Record all Adverse Events that occur during the study period (may be. defined as ‘from signing consent to conclusion of study participation’. Elicit adverse event information by asking open-ended questions, e.g.
[DOC File]Adverse Event Summary Page
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Adverse Event Start Date Stop Date Staff Initials/PI Initials / / / / / / / 15-Apr-13. Title: Adverse Event Summary Page Author: knechtej Last modified by: Kathleen Wessman Created Date: 4/10/2013 6:49:00 PM Company: LHSC Other titles: Adverse Event Summary Page ...
[DOC File]SITE VISIT LOG
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ADVERSE EVENT LOG _____ Page 1 of 1. This template document has been freely provided by The Global Health Network. Please adapt it as necessary for your work, and reference The Global Health Network when possible when using this template. www.theglobalhealthnetwork.org.
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