Summary of Original Version

Create a new section of KRS 217.005 to 217.215 to require that any person who administers an unapproved drug, devise, or biologic that has been approved for emergency use by the secretary of the United States Food and Drug Administration provides information to the individual receiving the unapproved drug, devise, or biologic; prohibit any person from requiring an individual to have an unapproved drug, devise, or biologic administered to him or her; EMERGENCY.