Section 460 IAC 6-25-6 - Monitoring of medication side effectsAuthority: IC 12-9-2-3; IC 12-11-1.1-9; IC 12-11-2.1-12
Affected: IC 12-11-1.1; IC 12-11-2.1
Sec. 6.
(a) The provider designated in section 1 of this rule shall design a system to monitor side effects an individual may experience as a result of medication the individual takes.(b) The provider shall:(1) document the system in writing; and(2) distribute the document to all providers working with the individual.(c) The system required in subsection (a) shall contain at least the following elements: (1) Training of direct care staff, employees, and agents concerning:(A) the identification of:(ii) interactions; of all medication administered to an individual; and(B) instruction on medication side effects and interactions.(2) A side effect tracking record that includes:(A) how often the individual should be monitored for side effects of each medication administered to the individual;(B) who shall perform the monitoring; and(C) when monitoring shall be performed.(3) A system for communication among all providers working with an individual regarding the monitoring of medication side effects.(d) All providers working with an individual shall:(2) comply with; the medication side effect monitoring system designed by the provider designated in section 1 of this rule.Division of Disability and Rehabilitative Services; 460 IAC 6-25-6; filed Nov 4, 2002, 12:04 p.m.: 26 IR 781; readopted filed Sep 26, 2008, 11:11 a.m.: 20081015-IR-460080618RFA; Readopted filed 8/11/2014, 11:20 a.m.: 20140910-IR-460140241RFAReadopted filed 11/9/2020, 3:08 p.m.: 20201209-IR-460200501RFA