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The data collector did not participate in the injection procedure, and a single investigator completed all statistical analyses

National Natural Science Foundation of China (Ref No

[DOI] [PMC free article] [PubMed] [Google Scholar] 68.Guan R, Yuan L, Li J, Wang J, Li Z, Cai Z, et al

In addition to the safety communication, FDA is requiring that 1) new warnings about the risk of respiratory depression be added to the prescribing information of the gabapentinoids, and 2) drug manufacturers conduct clinical trials to further evaluate abuse potential of the gabapentinoids, particularly in combination with opioids, because misuse and abuse of these products together is increasing, and co-use may increase the risk of respiratory depression