The Adverse Event Following Immunization has been created
Adverse Event Following Immunization

MINISTRY OF HEALTH

National Vaccines and Immunization Program

Adverse Event Following Immunization Reporting Form

Adverse Event Following Immunization
Adverse Event Following Immunization

Tip: Fields marked with * are mandatory

Form ID: new
Important Unique Form ID
Initial (Initial Report: new)

PATIENT DETAILS

-- clear!

If selected, year is mandatory.

--OR--

(static, mass, outreach)

(If patient is a child)

(self or nearest contact)



TYPE OF Adverse Event Following Immunization

:

(Signs & Symptoms)

(including timeline of occurrence)


Suspected Vaccine(s)

(e.g. BCG, DPT-Hib-HeB) (e.g. Dose 1, 2) Route of vaccination
(i.m.,s.c., i.d.)
Manufacturer's Name Expiry date #

Including history of similar reaction or other allergies, concomitant medication/vaccine,concomitant illness, other cases,pregnacy status and other relevant information


clear!
clear!

Action Taken:

(specify)

Specimen collected for investigation (specify type(s) of specimen)


clear!
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# File Text Description
Is the person submitting different from reporter? 
  




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