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Quality of Reporting of Bioequivalence Trials Comparing Generic to Brand Name Drugs: A Methodological Systematic Review

Overview of attention for article published in PLOS ONE, August 2011
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Title
Quality of Reporting of Bioequivalence Trials Comparing Generic to Brand Name Drugs: A Methodological Systematic Review
Published in
PLOS ONE, August 2011
DOI 10.1371/journal.pone.0023611
Pubmed ID
Authors

Amélie van der Meersch, Agnès Dechartres, Philippe Ravaud

Abstract

Generic drugs are used by millions of patients for economic reasons, so their evaluation must be highly transparent.

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The data shown below were collected from the profiles of 9 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 57 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 2 4%
India 1 2%
Unknown 54 95%

Demographic breakdown

Readers by professional status Count As %
Researcher 9 16%
Student > Master 8 14%
Student > Bachelor 8 14%
Other 6 11%
Professor 4 7%
Other 16 28%
Unknown 6 11%
Readers by discipline Count As %
Medicine and Dentistry 27 47%
Pharmacology, Toxicology and Pharmaceutical Science 6 11%
Agricultural and Biological Sciences 6 11%
Social Sciences 2 4%
Business, Management and Accounting 1 2%
Other 5 9%
Unknown 10 18%