Pragmatic pharmacoeconomic analyses by using post-market adverse drug reaction reports: an illustration using infliximab, adalimumab, and the Canada vigilance adverse reaction database
Abstract Background The prediction of the real-world cost of adverse drug reactions (ADRs) has historically relied on the data from randomized controlled trials (RCT). However, trial conditions do not always reflect the real-world applications of pharmaceutical products; hence, they may not accurate...
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Main Authors: | Tuhin Maity (Author), Christopher Longo (Author) |
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Format: | Book |
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BMC,
2021-11-01T00:00:00Z.
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Online Access: | Connect to this object online. |
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