Abstract: Objective To improve the quality of adverse drug reactions reporting via the rapid reporting system, and to promote pharmaceutical care. Methods After the construction of an ADR reporting system, adverse drug reactions in our hospital were retrospectively analyzed in terms of quantity and quality and clinical pharmaceutical safety service. Results After application of the ADR reporting system, the total number of standard reports of ADRs increased from 112 in 2014 to 641 in 2018. The first pass yield was increased from 17.48% in 2014 to 80.87% in 2018. About 99.69% of ADR reports in 2018 were qualified, compared with 78.32% in 2014. The timeliness (<3 d) of reporting of ADRs increased from 0.89% in 2014 to 53.82% in 2018. Conclusion The ADR reporting system in our hospital can contribute to the efficiency of reports, ensure the quality of reports and enhance supervision of drug safety.

Key words: adverse drug reactions, informationalized system, pharmaceutical care, drug safety