⚕ PharmaNotes — AEFI Report

Report of Adverse Event Following Immunization · Public Health Ontario
Please correct the following:
1 — CLIENT AND REPORTING SOURCE INFORMATION

2 — IMMUNIZATION INFORMATION
Date (yyyy-mm-dd) * Time (HH:MM) Manufacturer / Trade Name * Lot # Lot Exp. Date Dose # Site Route

*Describe in Section 5

3 — ADVERSE EVENT INFORMATION
A. Report only events which cannot be attributed to co-existing conditions.
B. Reactions marked must be diagnosed by a physician or nurse practitioner.
C. Record time to onset (from vaccination) and duration in minutes, hours, or days.
4 — MEDICAL HISTORY

Provide a detailed description of the client's medical history (e.g. immunocompromised, chronic illness, concomitant medications, history of allergies).

*Describe in Section 5

5 — COMMENTS FURTHER DESCRIBING THE ADVERSE EVENT(S)

Provide a detailed description including all signs and symptoms, investigation, treatment, hospitalization details, and description of previous AEFI or immunization error.

6 — HEALTH CARE UTILIZATION & OUTCOME

Outcome to be updated by the Public Health Unit when investigation is complete.