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Efficacy and safety of generic paroxetine tablets in centralized drug procurement: a real-world study

Published on Jan. 15, 2023Total Views: 805 times Total Downloads: 281 times Download Mobile

Author: Fei JIA 1, 2 Yan-Nan ZANG 1, 2 Meng-Xi NIU 1, 2 Shan-Shan LIU 1, 2 Hong-Yan ZHUANG 1, 2 guowe@ccmu.edu.cn Wei GUO 1, 2

Affiliation: 1. Beijing Anding Hospital, Capital Medical University, The National Clinical Research Center for Mental Disorders & Beijing Key Laboratory of Mental Disorders, Beijing 100088, China 2. Advanced Innovation Center for Human Brain Protection, Capital Medical University, Beijing 100069, China

Keywords: Drug centralized procurement Paroxetine Efficacy Safety Real-world study

DOI: 10.19960/j.issn.1005-0698.202301003

Reference: Fei JIA, Yan-Nan ZANG, Meng-Xi NIU, Shan-Shan LIU, Hong-Yan ZHUANG, Wei GUO.Efficacy and safety of generic paroxetine tablets in centralized drug procurement: a real-world study[J].Yaowu Liuxingbingxue Zazhi,2023, 32(1): 18-24.DOI: 10.19960/j.issn.1005-0698.202301003.[Article in Chinese]

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Abstract

Objective  To compare the the efficacy and safety of paroxetine tablet in the treatment of depressive disorder with centralized procurement of generic drug (LeYou®) and branded drug (Seroxat®). To evaluate the effects of drug centralized procurement policy on doctors’ prescribing behavior and patients’ treatment expenses, and to provide a basis for promoting the rational use of the generic drugs.

Methods  To extract the outpatient data of patients who were prescribed paroxetine tablets in the first half year after the implementation of the drug centralized procurement policy and in the same period of the previous year from Hospital Information System (HIS) of a Grade 3A psychiatric hospital. The relevant data were divided into generic drug and branded drug groups and analyzed by Propensity Score Match (PSM). The dosage, blood concentration, abnormal incidence of common adverse reaction, dressing change rate and drug cost of the generic drug and branded drug in clinical use were compared.

Results  There was no signifi-cant difference in drug dosage and blood concentration between the generic drug group and the branded drug group (P>0.05). There was no significant difference in the incidence of adverse drug reactions such as abnormal liver and kidney function, blood glucose increase, dyslipidemia and prolactin elevation between the generic drug group and the branded drug group (P>0.05). In the test period, the replace drug rate of the branded drug to the generic drug was 5.52%, and that of the reference period was 2.87%. In the two periods, about 0.59% and 0.48% of the patients changed to the branded research drug, respectively. The generic drug cost of patients in the test period was 310.38 yuan per time and the total drug cost was 1 052.77 yuan, which were significantly lower than the generic drug cost and the total drug cost in the reference period (P<0.01).

Conclusion  No significant difference was found in safety and efficacy between the generic drug of paroxetine tablet and the branded drug, and the generic drug had great economic advantages.

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References

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