Evidence map›Paper›PMID 40610517›Full record

ArticleScientific reports2025

Factors associated with the completeness of information provided in adverse drug reaction reports of physicians, pharmacists and consumers from Germany.

Diana Dubrall, Patrick Christ, Severin Domgörgen, Matthias Schmid, Bernhardt Sachs

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Diana DubrallInstitute for Medical Biometry, Informatics and Epidemiology, University Hospital Bonn, Venusberg-Campus 1, 53127, Bonn, Germany. Diana.Dubrall@bfarm.de.ORCID http://orcid.org/0000-0002-8763-051X
Patrick ChristInstitute for Medical Biometry, Informatics and Epidemiology, University Hospital Bonn, Venusberg-Campus 1, 53127, Bonn, Germany.ORCID http://orcid.org/0000-0003-3197-5639
Severin DomgörgenInstitute for Medical Biometry, Informatics and Epidemiology, University Hospital Bonn, Venusberg-Campus 1, 53127, Bonn, Germany.
Matthias SchmidInstitute for Medical Biometry, Informatics and Epidemiology, University Hospital Bonn, Venusberg-Campus 1, 53127, Bonn, Germany.ORCID http://orcid.org/0000-0002-0788-0317
Bernhardt SachsResearch Division, Federal Institute for Drugs and Medical Devices (BfArM), Kurt-Georg-Kiesinger-Allee 3, 53175, Bonn, Germany.ORCID http://orcid.org/0000-0001-8260-0891

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to identify factors associated with the completeness of spontaneous reports of adverse drug reactions (ADR) from different reporter types. We analysed 69,976 spontaneous ADR reports from physicians, 42,396 from pharmacists and 121,144 from consumers. The adjusted vigiGrade completeness score for ADR reports from EudraVigilance was used to evaluate the completeness of information provided in the structured format of each ADR report. Mean values of the vigiGrade completeness scores were calculated for various factors such as age, sex, receive year, seriousness and causal relationship. For all three reporters, the completeness of the ADR reports referring to older patients and children/ adolescents was lower than for middle-aged patients. Furthermore, generally poorly documented reports often included more than one suspected/interacting drug or no information on the patients' sex. Additionally, ADR reports with an at least possible causal relationship were more completely documented than those with a not assessable causal relationship in a subset of 479 ADR individually assessed reports. Differences between the reporters were only observed regarding seriousness criteria and receive year. The missing of certain information parameters in ADR reports from all three reporter types may serve as indicators for a poorer overall completeness of documentation.

Indexed as

Adverse Drug Reaction Reporting SystemsDrug-Related Side Effects and Adverse ReactionsPharmacistsPhysiciansAdolescentAdultAgedChildFemaleGermanyHumansMaleMiddle AgedPharmacovigilanceYoung AdultAdverse drug reactionsCompleteness of documentationReporter typesSpontaneous reporting databaseSpontaneous reports

Identifiers

PMID40610517
PMCPMC12229551

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.