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Yoshimoto, F
That one data point, that single difference in starting dose , changed the entire side effect profile for a meaningful percentage of trial participants
The PLA provides a presumption that FDA-approved labels are adequate, and although that presumption can be rebutted (defeated) by plaintiffs, the presumption provides pharmaceutical companies greater protection under New Jersey law compared to many other states
Bibcode:2018Natur.554..311W
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