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Drug-induced liver injury following the use of tocilizumab or sarilumab in patients with coronavirus disease 2019.
Gao, Qian; Yin, Xuedong; Tan, Boyu; Wang, Junshi; Chen, Jiayan; Zhao, Bin; Yang, Qiaoling; Li, Zhiling.
  • Gao Q; Department of Pharmacy, Shanghai Children's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200062, China.
  • Yin X; School of Medicine, Shanghai Jiao Tong University, Shanghai, 200125, China.
  • Tan B; Department of Pharmacy, Shanghai Children's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200062, China.
  • Wang J; School of Medicine, Shanghai Jiao Tong University, Shanghai, 200125, China.
  • Chen J; Department of Pharmacy, Shanghai Children's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200062, China.
  • Zhao B; Macau University of Science and Technology, Macau, China.
  • Yang Q; School of Nursing and Health, Shanghai Zhongqiao Vocational and Technical University, Shanghai, 201514, China.
  • Li Z; Department of Pharmacy, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, 100730, China.
BMC Infect Dis ; 22(1): 929, 2022 Dec 12.
Article in English | MEDLINE | ID: covidwho-2162307
ABSTRACT
BACKGROUNDS Interleukin-6 (IL-6) blockers including tocilizumab and sarilumab were approved by the U.S. Food and Drug Administration (FDA) in June 2021 for the treatment of patients with moderate to severe COVID-19. The use of sarilumab or tocilizumab in COVID-19 patients has been related to a reduction in mortality compared to standard care. Recent evidence has emerged concerning drug-induced liver injury (DILI) after sarilumab or tocilizumab applications in COVID-19 patients.

AIMS:

The study aimed to estimate DILI associated with sarilumab or tocilizumab in treating moderate to severe patients infected with SARS-Cov-2.

METHODS:

We conducted a retrospective pharmacovigilance study by data mining of the FDA's adverse event reporting systems (FAERS) database from the first quarter of 2004 to the fourth quarter of 2021 in confirmed COVID-19 patients. We analyzed DILI cases associated with tocilizumab or sarilumab in treating COVID-19 patients from the FAERS during this period. Disproportionality analysis and Bayesian analysis of COVID-19 patients were utilized for case analysis, and we also next compared the onset time and fatality rates of DILI following tocilizumab or sarilumab.

RESULTS:

A total of 275 cases of TCZ or SAR-related DILI reports were extracted. A total of 192 AEs cases were related to tocilizumab (TCZ), and 83 were related to sarilumab (SAR). In patients treated with TCZ, most were < 75 years old (51.57%), with more male than female (46.35% vs. 13.02%). The correlation between IL-6 receptor antagonists and DILI was stronger in SAR (ROR = 12.94; 95%CI 9.6-17.44) than in TCZ (ROR = 1.33; 95%CI 1.14-1.55). The onset time of DILI was different between TCZ and SAR, and a significant difference was observed in TCZ than SAR (P < 0.0001). A significant difference was observed in the mortality rate of TCZ and SAR (P = 0.0009). DILI associated with COVID-19 patients treated with TCZ appeared to have earlier onset-time (1(0-46) day) VS. SAR (3.5(0-27) day).

CONCLUSION:

This study shows strict monitor ought to be paid for TCZ or SAR when used for COVID-19 patients with poor liver function.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Chemical and Drug Induced Liver Injury / COVID-19 Type of study: Observational study / Prognostic study / Reviews Limits: Aged / Female / Humans / Male Language: English Journal: BMC Infect Dis Journal subject: Communicable Diseases Year: 2022 Document Type: Article Affiliation country: S12879-022-07896-0

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Chemical and Drug Induced Liver Injury / COVID-19 Type of study: Observational study / Prognostic study / Reviews Limits: Aged / Female / Humans / Male Language: English Journal: BMC Infect Dis Journal subject: Communicable Diseases Year: 2022 Document Type: Article Affiliation country: S12879-022-07896-0