20 CSR 2220-2.170
Procedure for Impaired Pharmacist
PURPOSE: This rule establishes an efficient and timely process
for the disposition of information and tentative board action
concerning impaired pharmacists to the attorney general’s
office for purposes of preparing a complaint and streamlines
the procedure utilized in interviewing pharmacists who are
chemically impaired.
(1) The executive director shall receive information concerning
the impairment of licensees and coordinate any investigations
that seek to substantiate information concerning a possible
impairment.
(2) Investigations by board inspectors or division investigators
concerning chemically impaired licensees will be collected and
reviewed by the executive director. Cases will be divided into
two (2) categories.
(A) Category A. Chemically impaired licensees where
additional information is evident that known distribution of
AND INSURANCE
controlled substances or legend drugs to other individuals has
taken place.
(B) Category B. Chemical impairment of a licensee where
controlled substances, legend drugs or alcohol have been
acquired for personal use only.
(3) Cases which fall into Category A will be referred to the board
for appropriate action.
(4) Cases which fall within Category B will be subject to
administrative review as a preliminary action to facilitate any
corrective actions deemed necessary by the board.
(5) The following shall constitute office procedures involving
Category B cases:
(A) Normal procedures for completing field investigations
and assimilating other pertinent information will be followed;
(B) If the director believes that a case falls into Category B of
this policy, s/he shall consult with the president of the board
concerning the appropriateness of an administrative review;
(C) If approval by the president is given, the director shall take
actions necessary to set up a meeting with the licensee who is
the subject of the investigation. In addition, other individuals
such as legal counsel for the board may be asked to attend,
along with any staff member, as necessary;
(D) A statement concerning due process procedures and
the rights of the licensee will be read at the beginning of
the review meeting. A complete record of the administrative
review meeting shall be maintained by the board office. Notice
that the president of the board has been notified and that s/he
has given approval for an administrative fact-finding meeting
shall be entered into the record;
(E) A format during the fact-finding meeting will be followed
that allows the licensee to provide a statement of his/her own as
well as a question/answer period allowed to discuss the aspects
of the case centering on the chemical impairment issues or on
any related concerns about the individual’s ability to practice
pharmacy;
(F) After the fact-finding meeting is concluded, a summary
will be provided to each member of the board within the
appropriate agenda, along with recommendations from the
director as to any action to be taken. In addition, the president
will be contacted and provided any follow-up information
that could warrant changes in administrative procedures.
The president, by executive order, may initiate an affidavit to
the board attorney of an intent to file a complaint with the
Administrative Hearing Commission. Once an order is executed,
the information on the case shall be forwarded to the attorney
for necessary legal preparation; and
(G) The entire board shall consider the case in closed session
as to whether or not to file a complaint against the licensee
and consider the recommendations made as to terms. Once the
board authorizes a complaint, the attorney for the board shall
assure that the appropriate filings take place.
(6) When an impaired pharmacist is disciplined by the board
and a term of the discipline is that s/he participate in a chemical
dependence treatment program, the impaired pharmacist shall
select a program which meets the following guidelines:
(A) Persons who are involved in the treatment or counseling
of a Missouri board-licensed pharmacist must submit written
documentation of their credentials and qualifications to
provide treatment or counseling;
(B) A written agreement or contract must be provided and
executed between the counselor(s) and the licensee, outlining
the responsibilities of each party for a successful treatment and
monitoring program. The agreement must include a provision
for sharing information concerning all aspects of therapy
between the treatment facility or counselors, or both, and the
Missouri Board of Pharmacy;
(C) An initial evaluation report must be completed and
provided to the board outlining the licensee’s present state
of impairment, the recommended course(s) of treatment,
the beginning date of treatment and an assessment of future
prospects for recovery;
(D) A copy of the proposed treatment plan must be provided
to the board and must include a provision outlining the method
of referral to an appropriate after-care program;
(E) The counselor(s) must provide progress reports to the
board as follows:
1. Inpatient therapy—monthly reports;
2. Outpatient therapy—quarterly reports; and
3. After-care programs—semiannual reports;
(F) The treatment program must include randomized and
witnessed body fluid testing and analysis, with any drug
presence not supported by a valid prescription to be reported
to the Missouri Board of Pharmacy;
(G) The treatment program must include a provision for
reporting any violation of the treatment contract or agreement
by the licensee to the board; and
(H) All reports outlined in this protocol must be provided in
writing to the board for a counselor or treatment facility, or
both, to be approved for the treatment of a licensee undergoing
disciplinary board action.
AUTHORITY: sections 338.140, RSMo Supp. 1989 and 338.240,
RSMo 1986.* This rule originally filed as 4 CSR 220-2.170. Original
rule filed Oct. 1, 1987, effective Jan. 14, 1988. Amended: Filed Nov.
15, 1988, effective March 11, 1989. Moved to 20 CSR 2220-2.170,
effective Aug. 28, 2006.
*Original authority: 338.140, RSMo 1939, amended 1981, 1989 and 338.240, RSMo
1951.