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- W1997799955 abstract "US Food and Drug Administration (FDA) monitoring of the continued safety of marketed medical products depends greatly on spontaneous reporting of serious adverse events by health professionals. Despite its inherent limitations, the national postmarketing surveillance system provides vital information of clinical importance." @default.
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- W1997799955 date "1998-01-01" @default.
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- W1997799955 title "Limitations and strengths of spontaneous reports data" @default.
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- W1997799955 doi "https://doi.org/10.1016/s0149-2918(98)80007-6" @default.
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