Spending on postapproval drug safety.


Autoria(s): Ridley, DB; Kramer, JM; Tilson, HH; Grabowski, HG; Schulman, KA
Data(s)

01/03/2006

Formato

429 - 436

Identificador

http://www.ncbi.nlm.nih.gov/pubmed/16522583

25/2/429

Health Aff (Millwood), 2006, 25 (2), pp. 429 - 436

http://hdl.handle.net/10161/6397

1544-5208

Relação

Health Aff (Millwood)

10.1377/hlthaff.25.2.429

Tipo

Journal Article

Cobertura

United States

Resumo

Withdrawals of high-profile pharmaceuticals have focused attention on post-approval safety surveillance. There have been no systematic assessments of spending on postapproval safety. We surveyed drug manufacturers regarding safety efforts. Mean spending on postapproval safety per company in 2003 was 56 million dollars (0.3 percent of sales). Assuming a constant safety-to-sales ratio, we estimated that total spending on postapproval safety by the top twenty drug manufacturers was 800 million dollars in 2003. We also examined, using regression analysis, the relationship between the number of safety personnel and the number of initial adverse-event reports. This study offers information for the debate on proposed changes to safety surveillance.

Idioma(s)

ENG

Palavras-Chave #Costs and Cost Analysis #Drug Approval #Drug Industry #Humans #Product Surveillance, Postmarketing #Regression Analysis #Safety #United States