A real-world disproportionality analysis of FDA Adverse Event Reporting System (FAERS) events for baricitinib. Issue 11 (1st November 2020)
- Record Type:
- Journal Article
- Title:
- A real-world disproportionality analysis of FDA Adverse Event Reporting System (FAERS) events for baricitinib. Issue 11 (1st November 2020)
- Main Title:
- A real-world disproportionality analysis of FDA Adverse Event Reporting System (FAERS) events for baricitinib
- Authors:
- Peng, Ling
Xiao, Kui
Ottaviani, Silvia
Stebbing, Justin
Wang, Ying-Jie - Abstract:
- ABSTRACT: Background: Baricitinib is approved for the treatment of rheumatoid arthritis (RA). The authors retrospectively investigated adverse events (AEs) by data-mining a self-reporting database to better understand toxicities, especially since it has been used during the coronavirus disease 2019 (COVID-19) pandemic. Methods: A reporting odds ratio (ROR) was used to detect the risk signals from the data in the US Food and Drug Administration (FDA) adverse event reporting system database (FAERS). The definition relied on system organ class (SOCs) and preferred terms (PTs) by the Medical Dictionary for Regulatory Activities (MedDRA). Results: The search retrieved 1, 598 baricitinib-associated cases within the reporting period: 86 PTs with significant disproportionality were retained. Infections including 'herpes zoster, ' 'oral herpes, ' and 'herpes virus infection' were found at a similar rate to those reported in trials, and such events were rare. Reports emerged for several thrombotic adverse events, while these events were also rare. Unexpected safety signals as opportunistic infections were detected. Serious outcomes as death and life-threatening outcomes accounted for 9.76% of the reported cases. Conclusions: The incidence of these AEs does not appear above the background expected. These data are consistent with routine clinical observations and suggest the importance of pharmacovigilance.
- Is Part Of:
- Expert opinion on drug safety. Volume 19:Issue 11(2020)
- Journal:
- Expert opinion on drug safety
- Issue:
- Volume 19:Issue 11(2020)
- Issue Display:
- Volume 19, Issue 11 (2020)
- Year:
- 2020
- Volume:
- 19
- Issue:
- 11
- Issue Sort Value:
- 2020-0019-0011-0000
- Page Start:
- 1505
- Page End:
- 1511
- Publication Date:
- 2020-11-01
- Subjects:
- Baricitinib -- JAK inhibitor -- pharmacovigilance -- FAERS -- adverse event
Drugs -- Side effects -- Periodicals
Drugs -- Toxicology -- Periodicals
Chemotherapy -- Periodicals
615.704 - Journal URLs:
- http://informahealthcare.com/journal/eds ↗
http://informahealthcare.com ↗
http://ninetta.ashley-pub.com/vl=3523218/cl=72/nw=1/rpsv/journal/journal3_home.htm ↗ - DOI:
- 10.1080/14740338.2020.1799975 ↗
- Languages:
- English
- ISSNs:
- 1474-0338
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3842.002945
British Library DSC - BLDSS-3PM
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- 22647.xml