We also collected information regarding notices of FDA regulatory actions readily available for the Federal Register22 as well as therapeutic class through the WHO Anatomical Therapeutic Chemical Classification System23 (Supplemental Table S1). We labeled the medication using the anatomical principal group. We chose the therapeutic subgroup for sys
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Additional quantitative analyses were not demanded, since we only regarded as success from correctly executed (Cochrane) opinions. The goal was to focus on specific outcomes such as the proportion of members with no less than fifty% pain reduction, all?cause or adverse event discontinuations, or significant adverse occasions, also to explore how th
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