Definition: An adverse event is defined as a death, life - threatening adverse drug or device experience, inpatient hospitalization or prolongation of existing hospitalization, a persistent disability/incapacity, or a congenital anomaly/birth defect.
Symptom presentation must have occurred within 1 week of HP x dosing be considered for review in our Adverse Events reporting process.
Patrons have three months to report an event. HPx Practitioners will interview and confirm the details of the Patrons Report and submit their own Practitioner Report. Both Reports will be reviewed and summarized by the FHCi Adverse Events Review Committee. Once reviewed they will be submitted to the FHCi Board for final review to either be a Published Adverse Event, or to be archived, within 60 days of original submission.