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Authors' Reply to Courtney Suggs and Colleagues’ Comment on: “Mixed Approach Retrospective Analyses of Suicide and Suicidal Ideation for Brand Compared with Generic Central Nervous System Drugs”

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The Original Article was published on 19 September 2018

The Original Article was published on 19 September 2018

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References

  1. Cheng N, Rahman MM, Alatawi Y, Qian J, Peissig PL, Berg RL, et al. Mixed approach retrospective analyses of suicide and suicidal ideation for brand compared with generic central nervous system drugs. Drug Saf. 2018;41(4):363–76.

    Article  CAS  Google Scholar 

  2. Suggs CM, Levin RL, Mosholder AD, Swain RS, Zhao L. Comment on: “Mixed approach retrospective analyses of suicide and suicidal ideation for brand compared with generic central nervous system drugs”. Drug Saf. 2018. https://doi.org/10.1007/s40264-018-0726-3.

    Article  PubMed  Google Scholar 

  3. U.S. Food and Drug Administration. FDA Adverse Events Reporting System (FAERS) Public Dashboard 2018. https://www.fda.gov/aboutfda/workingatfda/fellowshipinternshipgraduatefacultyprograms/pharmacystudentexperientialprogramcder/ucm591384.htm. Accessed 3 Sept 2018.

  4. U.S. Food and Drug Administration. FDA perspective on MedDRA® MedDRA® coding quality in postmarketing Safety Report 2012. https://www.meddra.org/sites/default/files/page/documents_insert/Informal_EU_MedDRA_Usergroup_31Oct2012_x.pdf. Accessed 3 Sept 2018.

  5. Kimura G, Kadoyama K, Brown JB, Nakamura T, Miki I, Nisiguchi K, et al. Antipsychotics-associated serious adverse events in children: an analysis of the FAERS database. Int J Med Sci. 2015;12(2):135–40.

    Article  CAS  Google Scholar 

  6. U.S. Food and Drug Administration. FDA List of Authorized Generic Drugs: U.S. Food Drug Administration. 2015. http://www.fda.gov/drugs/developmentapprovalprocess/howdrugsaredevelopedandapproved/approvalapplications/abbreviatednewdrugapplicationandagenerics/ucm126389.htm. Accessed 3 Sept 2018.

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Correspondence to Richard A. Hansen.

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Funding

No sources of funding were used to prepare this letter. The US FDA supported the study described in the original paper [1]. Views expressed in written materials or publications and by speakers do not necessarily reflect the official policies of the Department of Health and Human Services; nor does any mention of trade names, commercial practices, or organization imply endorsement by the United States Government.

Conflict of interest

In the past 3 years, Richard Hansen has provided expert testimony for Daiichi Sankyo. Ning Cheng, Md. Motiur Rahman, Yasser Alatawi, Jingjing Qian, Peggy L. Peissig, Richard L. Berg, and David Page have no conflicts of interest that are directly relevant to the content of this study.

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Hansen, R.A., Cheng, N., Rahman, M.M. et al. Authors' Reply to Courtney Suggs and Colleagues’ Comment on: “Mixed Approach Retrospective Analyses of Suicide and Suicidal Ideation for Brand Compared with Generic Central Nervous System Drugs”. Drug Saf 41, 1423–1424 (2018). https://doi.org/10.1007/s40264-018-0728-1

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  • DOI: https://doi.org/10.1007/s40264-018-0728-1

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