All abortion providers must report each procedure as defined in KRS 311.720 to the Department for Public Health, Vital Statistics Branch. Reports must be received within 15 days of the end of the month in which the abortion occurs.
If the abortion occurs in an institution, the head of the institution must file this report. If the abortion was performed outside an institution, the attending physician must file the report. The report must provide all information cited in KRS 311.782.
Institution heads and physicians must report each prescription issued for RU-486, cytotec, pitocin, mifeprex, misoprostol and other drugs or combinations of drugs for which the primary indication is induction of abortion as defined in KRS 311.720. This report must occur within 15 days of the end of the month in which the prescription was issued.
The name of the person completing the report and the reporting institution are not subject to disclosure under KRS 61.870 to 61.884.
By Sept. 30 of each year, the Vital Statistics Branch will issue a public report on all data collected that calendar year per KRS 213.101, subsections (1) and (2).