Construct and concurrent validity of a patient-reported adverse drug event questionnaire: a cross-sectional study-Reference-Cited by-同舟云学术

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Construct and concurrent validity of a patient-reported adverse drug event questionnaire: a cross-sectional study

Published:2014-08-13 Issue:1 Volume:12 Page:
ISSN:1477-7525
Container-title:Health and Quality of Life Outcomes
language:en
Short-container-title:Health Qual Life Outcomes

Author:

de Vries Sieta T,Haaijer-Ruskamp Flora M,de Zeeuw Dick,Denig Petra

Publisher

Springer Science and Business Media LLC

Subject

Public Health, Environmental and Occupational Health,General Medicine

Link

https://link.springer.com/content/pdf/10.1186/s12955-014-0103-6.pdf

Reference45 articles.

1. Suvarna V: Phase IV of drug development. Perspect Clin Res 2010, 1: 57–60.

2. Berlin JA, Glasser SC, Ellenberg SS: Adverse event detection in drug development: recommendations and obligations beyond phase 3. Am J Public Health 2008, 98: 1366–1371. 10.2105/AJPH.2007.124537

3. Walshe K: Adverse events in health care: issues in measurement. Qual Health Care 2000, 9: 47–52. 10.1136/qhc.9.1.47

4. Basch E, Iasonos A, McDonough T, Barz A, Culkin A, Kris MG, Scher HI, Schrag D: Patient versus clinician symptom reporting using the national cancer institute common terminology criteria for adverse events: results of a questionnaire-based study. Lancet Oncol 2006, 7: 903–909. 10.1016/S1470-2045(06)70910-X

5. Blenkinsopp A, Wilkie P, Wang M, Routledge PA: Patient reporting of suspected adverse drug reactions: a review of published literature and international experience. Br J Clin Pharmacol 2007, 63: 148–156. 10.1111/j.1365-2125.2006.02746.x

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