Literature DB >> 29215916

New and incremental FDA black box warnings from 2008 to 2015.

Michael T Solotke1, Sanket S Dhruva2,3,4, Nicholas S Downing5, Nilay D Shah6, Joseph S Ross2,7,8,9.   

Abstract

BACKGROUND: The boxed warning (also known as 'black box warning [BBW]') is one of the strongest drug safety actions that the U.S. Food & Drug Administration (FDA) can implement, and often warns of serious risks. The objective of this study was to comprehensively characterize BBWs issued for drugs after FDA approval.
METHODS: We identified all post-marketing BBWs from January 2008 through June 2015 listed on FDA's MedWatch and Drug Safety Communications websites. We used each drug's prescribing information to classify its BBW as new, major update to a preexisting BBW, or minor update. We then characterized these BBWs with respect to pre-specified BBW-specific and drug-specific features.
RESULTS: There were 111 BBWs issued to drugs on the US market, of which 29% (n = 32) were new BBWs, 32% (n = 35) were major updates, and 40% (n = 44) were minor updates. New BBWs and major updates were most commonly issued for death (51%) and cardiovascular risk (27%). The new BBWs and major updates impacted 200 drug formulations over the study period, of which 64% were expected to be used chronically and 58% had available alternatives without a BBW.
CONCLUSIONS: New BBWs and incremental updates to existing BBWs are frequently added to drug labels after regulatory approval.

Entities:  

Keywords:  Black box warning; boxed warning; drug labeling; drug safety; food and drug administration

Mesh:

Year:  2017        PMID: 29215916      PMCID: PMC6013049          DOI: 10.1080/14740338.2018.1415323

Source DB:  PubMed          Journal:  Expert Opin Drug Saf        ISSN: 1474-0338            Impact factor:   4.250


  14 in total

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Authors:  Laura Winterfield; Ruth Ann Vleugels; Kelly K Park
Journal:  J Drugs Dermatol       Date:  2015-07       Impact factor: 2.114

2.  Evaluation of FDA safety-related drug label changes in 2010.

Authors:  Jean Lester; George A Neyarapally; Earlene Lipowski; Cheryl Fossum Graham; Marni Hall; Gerald Dal Pan
Journal:  Pharmacoepidemiol Drug Saf       Date:  2013-01-02       Impact factor: 2.890

Review 3.  Impact of FDA drug risk communications on health care utilization and health behaviors: a systematic review.

Authors:  Stacie B Dusetzina; Ashley S Higashi; E Ray Dorsey; Rena Conti; Haiden A Huskamp; Shu Zhu; Craig F Garfield; G Caleb Alexander
Journal:  Med Care       Date:  2012-06       Impact factor: 2.983

4.  Era of faster FDA drug approval has also seen increased black-box warnings and market withdrawals.

Authors:  Cassie Frank; David U Himmelstein; Steffie Woolhandler; David H Bor; Sidney M Wolfe; Orlaith Heymann; Leah Zallman; Karen E Lasser
Journal:  Health Aff (Millwood)       Date:  2014-08       Impact factor: 6.301

5.  Trends in boxed warnings and withdrawals for novel therapeutic drugs, 1996 through 2012.

Authors:  Christine M Cheng; Jaekyu Shin; B Joseph Guglielmo
Journal:  JAMA Intern Med       Date:  2014-10       Impact factor: 21.873

6.  Evaluation of Pre-marketing Factors to Predict Post-marketing Boxed Warnings and Safety Withdrawals.

Authors:  Andreas Schick; Kathleen L Miller; Michael Lanthier; Gerald Dal Pan; Clark Nardinelli
Journal:  Drug Saf       Date:  2017-06       Impact factor: 5.606

7.  Clinical trial evidence supporting FDA approval of novel therapeutic agents, 2005-2012.

Authors:  Nicholas S Downing; Jenerius A Aminawung; Nilay D Shah; Harlan M Krumholz; Joseph S Ross
Journal:  JAMA       Date:  2014 Jan 22-29       Impact factor: 56.272

8.  Adherence to black box warnings for prescription medications in outpatients.

Authors:  Karen E Lasser; Diane L Seger; D Tony Yu; Andrew S Karson; Julie M Fiskio; Andrew C Seger; Nidhi R Shah; Tejal K Gandhi; Jeffrey M Rothschild; David W Bates
Journal:  Arch Intern Med       Date:  2006-02-13

9.  Postmarket Safety Events Among Novel Therapeutics Approved by the US Food and Drug Administration Between 2001 and 2010.

Authors:  Nicholas S Downing; Nilay D Shah; Jenerius A Aminawung; Alison M Pease; Jean-David Zeitoun; Harlan M Krumholz; Joseph S Ross
Journal:  JAMA       Date:  2017-05-09       Impact factor: 56.272

10.  Participation of the elderly, women, and minorities in pivotal trials supporting 2011-2013 U.S. Food and Drug Administration approvals.

Authors:  Nicholas S Downing; Nilay D Shah; Joseph H Neiman; Jenerius A Aminawung; Harlan M Krumholz; Joseph S Ross
Journal:  Trials       Date:  2016-04-14       Impact factor: 2.279

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Authors:  Giulia Callegaro; Steven J Kunnen; Panuwat Trairatphisan; Solène Grosdidier; Marije Niemeijer; Wouter den Hollander; Emre Guney; Janet Piñero Gonzalez; Laura Furlong; Yue W Webster; Julio Saez-Rodriguez; Jeffrey J Sutherland; Jennifer Mollon; James L Stevens; Bob van de Water
Journal:  Arch Toxicol       Date:  2021-10-09       Impact factor: 5.153

7.  Adverse Drug Reactions Associated With Drugs Prescribed in Psychiatry: A Retrospective Descriptive Analysis in a Tertiary Care Hospital.

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8.  Characterization and corroboration of safety signals identified from the US Food and Drug Administration Adverse Event Reporting System, 2008-19: cross sectional study.

Authors:  Meera M Dhodapkar; Xiaoting Shi; Reshma Ramachandran; Evan M Chen; Joshua D Wallach; Joseph S Ross
Journal:  BMJ       Date:  2022-10-05

9.  MitoToxy assay: A novel cell-based method for the assessment of metabolic toxicity in a multiwell plate format using a lactate FRET nanosensor, Laconic.

Authors:  Yasna Contreras-Baeza; Sebastián Ceballo; Robinson Arce-Molina; Pamela Y Sandoval; Karin Alegría; Luis Felipe Barros; Alejandro San Martín
Journal:  PLoS One       Date:  2019-10-31       Impact factor: 3.240

10.  Using an Automated Algorithm to Identify Potential Drug-Induced Liver Injury Cases in a Pharmacovigilance Database.

Authors:  Liliam Pineda Salgado; Ritu Gupta; Michael Jan; Osman Turkoglu; Alvin Estilo; Vinu George; Mirza I Rahman
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