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Letters |

Time for Action on Drug Safety

Deborah Shatin, PhD; Jacqueline S. Gardner, PhD; Andy Stergachis, PhD
JAMA. 1999;281(4):319-322. doi:10-1001/pubs.JAMA-ISSN-0098-7484-281-4-jbk0127.
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To the Editor: The Commentary by Mr Moore and colleagues1 on the need for better postmarketing drug surveillance raises important issues. We agree with the need for a "more active and effective safety program for marketed drugs." With an estimated 2 million hospital patients experiencing serious adverse drug reactions (ADRs) and 100,000 having fatal ADRs in 1994,2 and with increasing numbers of new drug approvals, the ability of the government to protect the public health is increasingly challenged. This is particularly salient since approximately 48% of the currently available prescribed drugs came on the market after 1990 with an accelerating rate of new drug approvals.3

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