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This deficiency of strong evidence of patient benefits is exemplified in the case of certified infectious disease products and solutions (QIDP). The FDA can approve a new antibiotic with no added clinical benefit for an “unmet health care want” with no proof demonstrating extra Positive aspects for those sufferers, since the antibiotic may be p

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We also gathered information about notices of FDA regulatory actions readily available in the Federal Register22 and the therapeutic course from your WHO Anatomical Therapeutic Chemical Classification System23 (Supplemental Table S1). We labeled the prescription drugs using the anatomical key group. We chose the therapeutic subgroup for systemic an

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