State Budget Office
Office of Regulatory Reinvention
111 S. Capitol Avenue; 8th Floor, Romney Building,
Lansing, MI 48933
Phone: (517) 335-8658 FAX: (517) 335-9512
REQUEST FOR RULEMAKING (RFR)
Under the Administrative Procedures Act (APA), 1969 PA 306, the agency that has the statutory authority
to promulgate rules must electronically file a RFR with the Office of Regulatory Reinvention (ORR)
before initiating any changes or additions to the rules. Submit copy to the ORR at orr@michigan.gov.
1. Agency Information
Agency name: Health and Human Services
Division/Bureau/Office: Bureau of Epidemiology and Population Health
517-284-4910
2. Rule Set Information
Title of proposed rule set: REPORTING OF POISONINGS DUE TO THE USE OF
PRESCRIPTION OR ILLICIT DRUGS
Rule number(s) or range of numbers: New Rule Set- Mich Admin Code R 325.76 to R 325.100.
Included in agency’s annual regulatory plan as rule to be processed in current year? Yes
3. Estimated timetable for completion, or statutory deadline, if applicable:
Six Months
4. Describe the general purpose of these rules, including any problem(s) the changes are intended to
address:
With the dramatic increase in the rise of overdoses and deaths caused by prescription medications
and illicit “street” drugs, tracking the information is difficult as there is no requirement that health
professionals and health facilities report this information. Without the information, the State is
unable to proportionately leverage resources to each county to combat the overdoes/death epidemic
occurring in this State. See latest statistics provided by Sparrow Hospital at
5. Cite the specific rule promulgation authority (i.e. agency director, commission, board, etc.,
listing all applicable statutory references. If the rule(s) are mandated by any applicable
constitutional or statutory provision, please explain.
By authority conferred on the department of health and human services by section 8 of 1978 PA
312; sections 2221, 2226, 2233, and 5111 of 1978 PA 368; and Executive Reorganization Order
No. 2015-1, being MCL 325.78, MCL 333.2221, MCL 333.2226, MCL 333.2233, MCL 333.5111,
and MCL 400.227.
6. Describe the extent to which the rule(s) conflict with, duplicate, or exceed similar regulations,
compliance requirements, or other standards adopted at the state, regional, or federal level.
Include applicable public act and statutory references.
The proposed rules do not conflict with, duplicate, or exceed similar regulations,
compliance requirements, or other standards adopted at the state, regional, or federal level.
7. Is the subject matter of the rule(s) currently contained in any guideline, manual, handbook,
instructional bulletin, form with instructions, or operational memo?
Revised: January 4, 2018
MCL 24.239