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For researchers and clinicians following this issue, this is the central question in the upcoming FDA decision: is dysesthesia frequent and debilitating enough to justify a special mention in the indications, or even a 12 mg dose reserved for specific patients

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Access this article Similar content being viewed by others Data availability The datasets generated and/or analyzed during the current study are available from the corresponding author on reasonable request

Penninckx MJ

Suggested metrics include: Percent reduction in calendar days to ATO decision Labor hours saved per control family Evidence re use rate across systems False positive versus true positive control failure detection Single monolithic solution or multiple micro apps