Below are detailed descriptions of reportable adverse events, grouped by state or federal agency. Answer the question that appears beneath EACH description. When you're finished, click View Reporting Instructions to move to the next page.
Please note that this section does not yet include reporting requirements for serious adverse drug events (SADEs) under M.G.L. c. 111, § 51H. DPH is expected to promulgate regulations to further specify reporting requirements related to SADEs. Updates will be posted here after they are available.