The reporting for adverse reactions has been streamlined to include a standard form for licensees to utilize when reporting adverse reactions to the agency. The form can be found here.
The administrative rules require adverse reactions to be reported to the agency and additionally in the statewide monitoring system. Please refer to this bulletin, which provides step by step instructions for how to enter the information.
For medical provisioning centers, the same bulletin instructions can be utilized with one modification – in the receipt number spot, the patient number will be recorded instead.