Literature DB >> 18207263

The risk we bear: the effects of review speed and industry user fees on new drug safety.

Mary K Olson1.   

Abstract

Drug review speed has increased substantially in the 1990s, largely due to industry-funded user fees. Following several drug withdrawals, however, new questions have emerged about the effects of this change on drug safety. This article examines the impact of review speed and user fees on counts of serious adverse reactions among drugs approved in 1990-2001. The analysis controls for the influence of drug utilization, patient conditions, drug novelty, black box warnings, foreign drug launch, US launch lags, patient age, and gender on drug reactions. Results show that drugs receiving faster reviews are associated with increased counts of serious adverse drug reactions. Other results show that novel drugs, drugs with black box warnings, drugs first launched abroad, and drugs with shorter US launch lags also have increased adverse drug reactions. Although any increase in risks must be weighed against benefits, the results show a trade-off between review speed and drug safety.

Entities:  

Mesh:

Year:  2007        PMID: 18207263     DOI: 10.1016/j.jhealeco.2007.10.007

Source DB:  PubMed          Journal:  J Health Econ        ISSN: 0167-6296            Impact factor:   3.883


  9 in total

1.  Cost recovery by Health Canada and drug safety: a time-series analysis.

Authors:  Joel Lexchin
Journal:  CMAJ Open       Date:  2018-10-18

2.  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

3.  Assessment of the impact of scheduled postmarketing safety summary analyses on regulatory actions.

Authors:  S Sekine; E E Pinnow; E Wu; R Kurtzig; M Hall; G J Dal Pan
Journal:  Clin Pharmacol Ther       Date:  2016-03-31       Impact factor: 6.875

4.  Enhancing prescription drug innovation and adoption.

Authors:  G Caleb Alexander; Alec B O'Connor; Randall S Stafford
Journal:  Ann Intern Med       Date:  2011-06-21       Impact factor: 25.391

Review 5.  A systematic review and critical assessment of incentive strategies for discovery and development of novel antibiotics.

Authors:  Matthew J Renwick; David M Brogan; Elias Mossialos
Journal:  J Antibiot (Tokyo)       Date:  2015-10-14       Impact factor: 2.649

6.  Trends in utilization of FDA expedited drug development and approval programs, 1987-2014: cohort study.

Authors:  Aaron S Kesselheim; Bo Wang; Jessica M Franklin; Jonathan J Darrow
Journal:  BMJ       Date:  2015-09-23

7.  Safety related label changes for new drugs after approval in the US through expedited regulatory pathways: retrospective cohort study.

Authors:  Sana R Mostaghim; Joshua J Gagne; Aaron S Kesselheim
Journal:  BMJ       Date:  2017-09-07

8.  Analysis of Safety-Related Regulatory Actions for New Drugs in Japan by Nature of Identified Risks.

Authors:  Makoto Fujikawa; Shunsuke Ono
Journal:  Pharmaceut Med       Date:  2017-07-13

9.  Unpacking the effects of adverse regulatory events: Evidence from pharmaceutical relabeling.

Authors:  Matthew J Higgins; Xin Yan; Chirantan Chatterjee
Journal:  Res Policy       Date:  2020-09-12
  9 in total

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