Evidence map›Paper›PMID 32978702›Full record

ArticleDrug safety2020

Sex Differences in Reported Adverse Drug Reactions to COVID-19 Drugs in a Global Database of Individual Case Safety Reports.

Alem Zekarias, Sarah Watson, Sara Hedfors Vidlin, Birgitta Grundmark

Abstract read
In one paragraph

Article in Drug safety, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Alem ZekariasUppsala Monitoring Centre, Uppsala, Sweden. alem.zekarias@who-umc.org.ORCID http://orcid.org/0000-0003-0297-8881
Sarah WatsonUppsala Monitoring Centre, Uppsala, Sweden.ORCID http://orcid.org/0000-0001-9660-5968
Sara Hedfors VidlinUppsala Monitoring Centre, Uppsala, Sweden.ORCID http://orcid.org/0000-0003-1619-3751
Birgitta GrundmarkUppsala Monitoring Centre, Uppsala, Sweden.ORCID http://orcid.org/0000-0002-2799-9374

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionIn late 2019, a new coronavirus-severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-was discovered in Wuhan, China, and the World Health Organization later declared coronavirus disease 2019 (COVID-19) a pandemic. Numerous drugs have been repurposed and investigated for therapeutic effectiveness in the disease, including those from "Solidarity," an international clinical trial (azithromycin, chloroquine, hydroxychloroquine, the fixed combination lopinavir/ritonavir, and remdesivir).

objectiveOur objective was to evaluate adverse drug reaction (ADR) reporting for drugs when used in the treatment of COVID-19 compared with use for other indications, specifically focussing on sex differences.

methodWe extracted reports on COVID-19-specific treatments from the global ADR database, VigiBase, using an algorithm developed to identify reports that listed COVID-19 as the indication. The Solidarity trial drugs were included, as were any drugs reported ≥ 100 times. We performed a descriptive comparison of reports for the same drugs used in non-COVID-19 indications. The data lock point date was 7 June 2020.

resultsIn total, 2573 reports were identified for drugs used in the treatment of COVID-19. In order of frequency, the most reported ADRs were electrocardiogram QT-prolonged, diarrhoea, nausea, hepatitis, and vomiting in males and diarrhoea, electrocardiogram QT-prolonged, nausea, vomiting, and upper abdominal pain in females. Other hepatic and kidney-related events were included in the top ten ADRs in males, whereas no hepatic or renal terms were reported for females. COVID-19-related reporting patterns differed from non-pandemic reporting for these drugs.

conclusionReview of a global database of suspected ADR reports revealed sex differences in the reporting patterns for drugs used in the treatment of COVID-19. Patterns of ADR sex differences need further elucidation.

Indexed as

COVID-19 Drug TreatmentAbdominal PainAdenosine MonophosphateAlanineAntibodies, Monoclonal, HumanizedAntiviral AgentsAzithromycinChemical and Drug Induced Liver InjuryChloroquineDatabases, PharmaceuticalDiarrheaDrug CombinationsDrug EruptionsDrug-Related Side Effects and Adverse ReactionsDrug RepositioningFemaleAdenosine MonophosphateAlanineAntibodies, Monoclonal, HumanizedAntiviral AgentsAzithromycinChloroquineDrug CombinationsHydroxychloroquineLopinavirlopinavir-ritonavir drug combinationOseltamivirremdesivirRitonavirtocilizumab

Identifiers

PMID32978702
PMCPMC7518652

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Registered trials

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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.