Publication:
Metamizole-associated adverse events: a systematic review and meta-analysis.

cris.virtualsource.author-orcid717d493b-96db-4872-8921-e96206509da3
cris.virtualsource.author-orcidcf0b2f7b-e021-4f70-af89-b4cb88c805a2
datacite.rightsopen.access
dc.contributor.authorKötter, Thomas
dc.contributor.authorDa Costa, Bruno
dc.contributor.authorFässler, Margrit
dc.contributor.authorBlozik, Eva
dc.contributor.authorLinde, Klaus
dc.contributor.authorJüni, Peter
dc.contributor.authorReichenbach, Stephan
dc.contributor.authorScherer, Martin
dc.date.accessioned2024-10-23T18:29:31Z
dc.date.available2024-10-23T18:29:31Z
dc.date.issued2015
dc.description.abstractBACKGROUND Metamizole is used to treat pain in many parts of the world. Information on the safety profile of metamizole is scarce; no conclusive summary of the literature exists. OBJECTIVE To determine whether metamizole is clinically safe compared to placebo and other analgesics. METHODS We searched CENTRAL, MEDLINE, EMBASE, CINAHL, and several clinical trial registries. We screened the reference lists of included trials and previous systematic reviews. We included randomized controlled trials that compared the effects of metamizole, administered to adults in any form and for any indication, to other analgesics or to placebo. Two authors extracted data regarding trial design and size, indications for pain medication, patient characteristics, treatment regimens, and methodological characteristics. Adverse events (AEs), serious adverse events (SAEs), and dropouts were assessed. We conducted separate meta-analyses for each metamizole comparator, using standard inverse-variance random effects meta-analysis to pool the estimates across trials, reported as risk ratios (RRs). We calculated the DerSimonian and Laird variance estimate T2 to measure heterogeneity between trials. The pre-specified primary end point was any AE during the trial period. RESULTS Of the 696 potentially eligible trials, 79 trials including almost 4000 patients with short-term metamizole use of less than two weeks met our inclusion criteria. Fewer AEs were reported for metamizole compared to opioids, RR = 0.79 (confidence interval 0.79 to 0.96). We found no differences between metamizole and placebo, paracetamol and NSAIDs. Only a few SAEs were reported, with no difference between metamizole and other analgesics. No agranulocytosis or deaths were reported. Our results were limited by the mediocre overall quality of the reports. CONCLUSION For short-term use in the hospital setting, metamizole seems to be a safe choice when compared to other widely used analgesics. High-quality, adequately sized trials assessing the intermediate- and long-term safety of metamizole are needed.
dc.description.noteKötter and da Costa contributed equally to this work.
dc.description.numberOfPages18
dc.description.sponsorshipBerner Institut für Hausarztmedizin (BIHAM)
dc.description.sponsorshipInstitut für Sozial- und Präventivmedizin (ISPM)
dc.identifier.doi10.7892/boris.68976
dc.identifier.pmid25875821
dc.identifier.publisherDOI10.1371/journal.pone.0122918
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/133399
dc.language.isoen
dc.publisherPublic Library of Science
dc.relation.ispartofPLoS ONE
dc.relation.issn1932-6203
dc.relation.organizationDCD5A442BECFE17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BDB9E17DE0405C82790C4DE2
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.subject.ddc300 - Social sciences, sociology & anthropology::360 - Social problems & social services
dc.titleMetamizole-associated adverse events: a systematic review and meta-analysis.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue4
oaire.citation.startPagee0122918
oaire.citation.volume10
oairecerif.author.affiliationBerner Institut für Hausarztmedizin (BIHAM)
oairecerif.author.affiliationInstitut für Sozial- und Präventivmedizin (ISPM)
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unibe.description.ispublishedpub
unibe.eprints.legacyId68976
unibe.journal.abbrevTitlePLOS ONE
unibe.refereedtrue
unibe.subtype.articlejournal

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