2022
DOI: 10.1016/j.heliyon.2022.e11782
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Severe ARDS due to Ruxolitinib discontinuation syndrome: case presentation and literature review

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Cited by 2 publications
(1 citation statement)
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“…433 Several studies have also reported that the rapid discontinuation of ruxolitinib administration induced life-threatening withdrawal symptoms, which may be attributed to robust changes in the activities of inflammatory cytokines. [434][435][436][437][438][439][440][441][442] The preferentially selective JAK3 and JAK1 inhibitor tofacitinib was the first JAK inhibitor approved for patients with RA that had poor responses to conventional drugs like methotrexate. 443,444 Several studies showed that tofacitinib was consistently more efficacious and safer compared with other DMARDs in patients with RA.…”
Section: (Covid-19mentioning
confidence: 99%
“…433 Several studies have also reported that the rapid discontinuation of ruxolitinib administration induced life-threatening withdrawal symptoms, which may be attributed to robust changes in the activities of inflammatory cytokines. [434][435][436][437][438][439][440][441][442] The preferentially selective JAK3 and JAK1 inhibitor tofacitinib was the first JAK inhibitor approved for patients with RA that had poor responses to conventional drugs like methotrexate. 443,444 Several studies showed that tofacitinib was consistently more efficacious and safer compared with other DMARDs in patients with RA.…”
Section: (Covid-19mentioning
confidence: 99%