Adverse Events Reporting Procedure

10.10: Adverse Events Reporting System: All potential adverse events will be assessed and reviewed for reportable Adverse Events. A tally of Adverse Event Reports and Reviews will be made public. After the review process if it is determined that in fact an Adverse Event has happened, non-PHI and details regarding the Adverse Event will be made public.

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.

10.11:  Adverse Event Liability: FHCi Patron Research Registrants accept the responsibilities and liabilities of their relationship within their HPx Practitioner’s Private practice which is outside of the jurisdiction of FHCi.

However, FHCi stands by the safety, efficacy, and reliability of HPx Programs and Homeopathic Protocols it develops. In addition, operates in transparency for any possible Adverse Event. Accordingly, in order to serve the public in transparency, if a Patron believes they or their children have adversely reacted to an HPx program or Homeopathic protocol in such a way that there may have been an Adverse Event then:

All Adverse events will be logged and made public on the website, withholding PHI (Personal Health Information) of the family Member and child in question and the name of the HP Supervisor.  Reported Adverse Events