“…In our study, the most common TRQ-related ADRs related to the skin and appendages, and the majority ADRs occurred within the first 2 h of TRQ administration, being similar to the results reported in previous studies (Shen et al, 2007;Li et al, 2010;Zhong et al, 2010;Xie et al, 2014;Wang et al, 2016;Wang et al, 2019). However, it is important to note that the incidences of TRQ-related AEs and ADRs seen in our study are higher than those seen in TRQ clinical trials (0.3% vs. 0.1~0.14%) (Shen et al, 2007;Li et al, 2010;Zhong et al, 2010;Xie et al, 2014;Wang et al, 2016), highlighting the importance of post-marketing surveillance. Our study included a broad range of patients, including those with a history of allergy, infants, and the elderly who were excluded from the TRQ clinical trials (Shanghai Kaibao Pharmaceutical Co., LTD, unpublished;Shen et al, 2007).…”