Evidence map›Paper›PMID 39578788›Full record

ArticleBMC psychiatry2024

Suicide-related risk among patients using branded and generic fluoxetine: a propensity score-matched, new-user design in Taiwan.

Cong-Wei Zheng, Yu-Chieh Huang, Yuan-Liang Wen, Hui-Wen Yang, Sheng-Yin To, Li-Ting Kao

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Article in BMC psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Cong-Wei ZhengDepartment of Pharmacy, Taichung Armed Forces General Hospital, Taichung, Taiwan.
Yu-Chieh Huang *Department of Psychiatry, Tri-Service General Hospital, Taipei, Taiwan.
Yuan-Liang WenSchool of Pharmacy, National Defense Medical Center, Taipei, Taiwan.
Hui-Wen YangSchool of Pharmacy, National Defense Medical Center, Taipei, Taiwan.
Sheng-Yin ToSchool of Pharmacy, National Defense Medical Center, Taipei, Taiwan.
Li-Ting Kao *School of Pharmacy, National Defense Medical Center, Taipei, Taiwan. kaoliting@office365.ndmctsgh.edu.tw.

Funding

Medical Affairs Bureau, Taiwan MND-MAB-C10-111038Tri-Service General Hospital TSGH-E-113292
6 · The paper itself

Abstract

backgroundTo date, the clinical equivalence between branded and generic medications remains debate and may sometimes be a reason why psychiatrists are hesitant to prescribe generic medications. Depression is recognized to exacerbate suicide risk globally and selective serotonin reuptake inhibitors, such as fluoxetine are common treatment options. Therefore, this study aimed to explores differences in suicidal risks between users of branded and generic fluoxetine in Taiwan.

methodsThis cohort study used Taiwan Longitudinal Health Insurance Database, encompassing 2 million individuals covered by National Health Insurance (NHI) program. The full cohort consisted of 32,298 fluoxetine new users. Then, 7,380 branded and 7,380 propensity score matched (PSM) generic fluoxetine new users were identified. The study further utilized Cox proportional hazards models to assess risk of 5-year suicidal ideation, suicide mortality, and all-cause mortality.

resultsThe study revealed that the adjusted hazard ratios (HRs) for suicidal ideation, suicide mortality and all-cause mortality in branded users were 0.766 (95% CI, 0.497 - 1.181), 0.660 (95% CI, 0.447 - 0.975), and 0.942 (95% CI, 0.849 - 1.045), respectively, when compared with matched generic fluoxetine users. Stratified and sensitivity analyses showed the lower risk of suicide mortality in specific subgroups, such as male (adjusted HRs = 0.536, 95% CI = 0.306-0.939) and young branded users (adjusted HRs = 0.549, 95% CI = 0.334-0.904).

conclusionThis study observed trends in the prevention effects of suicide-related risks. However, only suicide mortality was statistically significant, especially in males and those aged < 40 years. These insights may assist clinicians and policymakers in decision-making. CLINICAL TRIAL NUMBER: NA (This study is a cohort study utilizing the national health insurance database, not a clinical trial).

Indexed as

Drugs, GenericFluoxetinePropensity ScoreSuicideAdolescentAdultAgedCohort StudiesFemaleHumansMaleMiddle AgedProportional Hazards ModelsSelective Serotonin Reuptake InhibitorsSuicidal IdeationTaiwanDrugs, GenericFluoxetineSelective Serotonin Reuptake InhibitorsBrandedDepressionFluoxetineGenericSelective serotonin reuptake inhibitorsSuicide

Identifiers

PMID39578788
PMCPMC11583744

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.