Construct and concurrent validity of a patient-reported adverse drug event questionnaire: a cross-sectional study (Q34571228)

3 August 2017

title

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

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3 August 2017

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Sieta T de Vries

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3 August 2017

Flora M Haaijer-Ruskamp

series ordinal

2

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3 August 2017

Dick de Zeeuw

series ordinal

3

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3 August 2017

Petra Denig

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4

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3 August 2017

publication date

13 August 2014

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Health and Quality of Life Outcomes

3 August 2017

published in

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3 August 2017

volume

12

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3 August 2017

page(s)

103

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Standards of medical care in diabetes--2013

3 August 2017

cites work

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7 July 2018

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7 July 2018

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7 July 2018

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Information deficits in the summary of product characteristics preclude an optimal management of drug interactions: a comparison with evidence from the literature

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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Sensitivity and specificity and their confidence intervals cannot exceed 100%.

7 July 2018

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Diagnostic tests 2: Predictive values

7 July 2018

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7 July 2018

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How well do patient reports reflect adverse drug reactions reported by rheumatologists? Agreement of physician- and patient-reported adverse events in patients with rheumatoid arthritis observed in the German biologics register

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Consumers' reports of suspected adverse drug reactions volunteered to a consumer magazine

21 January 2018

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Impact of adverse drug reaction and predictivity of quality of life status in tuberculosis

21 January 2018

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Determinants of quality of life in type 2 diabetes population: the inclusion of personality.

21 January 2018

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Challenges using online surveys in a Danish population of people with type 2 diabetes

21 January 2018

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Medication Adherence Affects Treatment Modifications in Patients With Type 2 Diabetes

21 January 2018

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A qualitative study to explore how patients identify and assess symptoms as adverse drug reactions

21 January 2018

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12 December 2020

Development and Initial Validation of a Patient-Reported Adverse Drug Event Questionnaire

1 reference

12 December 2020

Adverse event detection in drug development: recommendations and obligations beyond phase 3

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12 December 2020

Estimating clinically significant differences in quality of life outcomes

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12 December 2020

Representativeness of diabetes patients participating in a web-based adverse drug reaction monitoring system

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12 December 2020

What is sufficient evidence for the reliability and validity of patient-reported outcome measures?

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12 December 2020

10.1186/S12955-014-0103-6

Identifiers

DOI

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Dimensions Publication ID

3 August 2017

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3 August 2017

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