Selected article for: "arbidol group and statistical difference"
Author: Chang Chen; Jianying Huang; Zhenshun Cheng; Jianyuan Wu; Song Chen; Yongxi Zhang; Bo Chen; Mengxin Lu; Yongwen Luo; Jingyi Zhang; Ping Yin; Xinghuan Wang
Title: Favipiravir versus Arbidol for COVID-19: A Randomized Clinical Trial
  • Document date: 2020_3_20
    • ID: 14he8n3u_32
    Snippet: During this trial, we detected 37 incidences of antiviral-associated adverse effects (AE) in the Favipiravir group and 28 incidences in the Arbidol group. All observed AE incidences were level 1. Favipiravir was associated with increased serum uric acid (3 (2.50%) in Arbidol group vs 16 (13.79%) in Favipiravir group, P=0.0014). No statistical difference was observed for the frequency of abnormal ALT/AST, psychiatric symptom reactions or digestive.....
    Document: During this trial, we detected 37 incidences of antiviral-associated adverse effects (AE) in the Favipiravir group and 28 incidences in the Arbidol group. All observed AE incidences were level 1. Favipiravir was associated with increased serum uric acid (3 (2.50%) in Arbidol group vs 16 (13.79%) in Favipiravir group, P=0.0014). No statistical difference was observed for the frequency of abnormal ALT/AST, psychiatric symptom reactions or digestive tract reactions ( Table 4 ). Most of these adverse reactions disappeared by the time patients being discharged.

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