Adverse event reporting in oncology clinical trials - lost in translation?
Author:
Funder
none
Publisher
Informa UK Limited
Subject
Pharmacology (medical),General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1080/14740338.2016.1175429
Reference18 articles.
1. Patient versus clinician symptom reporting using the National Cancer Institute Common Terminology Criteria for Adverse Events: results of a questionnaire-based study
2. Reporting of serious adverse events during cancer clinical trials to the institutional review board: An evaluation by theResearch onAdverseDrug eventsAndReports (RADAR) project
3. Completeness of Safety Reporting in Randomized Trials
4. Symptomatic Toxicities Experienced During Anticancer Treatment: Agreement Between Patient and Physician Reporting in Three Randomized Trials
5. How Accurate Is Clinician Reporting of Chemotherapy Adverse Effects? A Comparison With Patient-Reported Symptoms From the Quality-of-Life Questionnaire C30
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