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For providers, this matters because: - Malpractice insurers may not cover adverse events arising from administration of unapproved drugs - State medical boards can take disciplinary action against physicians administering unapproved substances outside a registered clinical trial - There's no FDA-reviewed safety and efficacy data to rely on as a legal defense if something goes wrong For patients, this matters because the protections you'd normally have β an FDA-reviewed safety profile, a pharmacovigilance system, standardized manufacturing requirements β don't apply to unapproved compounds
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