Get the free REPORT OF ADVERSE EVENTS FOLLOWING IMMUNIZATION (AEFI)

This report is intended for documenting any adverse events that occur following vaccination, especially those that meet specific criteria such as being serious, requiring urgent medical attention,

How to fill out report of adverse events

How to fill out REPORT OF ADVERSE EVENTS FOLLOWING IMMUNIZATION (AEFI)

1. Begin by collecting all necessary information about the patient, including name, age, and contact details.
2. Fill in the date of immunization and the vaccine received.
3. Record the date when the adverse event occurred.
4. Describe the adverse event in detail, including symptoms experienced.
5. Include any relevant medical history or pre-existing conditions of the patient.
6. Document any other medications or vaccines the patient may have received around the same time.
7. Provide information about the healthcare provider or facility reporting the event.
8. Sign and date the report to confirm that the information provided is accurate.

Who needs REPORT OF ADVERSE EVENTS FOLLOWING IMMUNIZATION (AEFI)?

1. Healthcare professionals administering vaccines.
2. Patients or caregivers who experience or witness an adverse event following immunization.
3. Public health officials monitoring vaccine safety.
4. Research institutions studying vaccine-related effects.

People Also Ask about

What are the types of AEFI for reporting?

Types of AEFI for Reporting For purpose of reporting, AEFIs can be minor, severe and serious. Common, self-limiting reactions, usually occur within a few hours of injection and resolve after short period of time and pose little danger. Examples: pain, swelling at injection site, fever, irritability, malaise etc.

What are the types of AEFI for reporting?

Types of AEFI for Reporting For purpose of reporting, AEFIs can be minor, severe and serious. Common, self-limiting reactions, usually occur within a few hours of injection and resolve after short period of time and pose little danger. Examples: pain, swelling at injection site, fever, irritability, malaise etc.

What is considered an adverse reaction to a vaccine?

An adverse event is an untoward event that occurs after a vaccination that might be caused by the vaccine product or vaccination process. These events range from common, minor, local reactions to rare, severe, allergic reactions (e.g., anaphylaxis).

What is AEFI reporting?

‎If your patient experiences an adverse event Health care providers including physicians and pharmacists are required by law to report Adverse Events Following Immunization (AEFI) to monitor vaccine safety.

What does AEFI stand for?

An adverse event following immunization (AEFI) is defined as any untoward medical occurrence following immunization which does not necessarily have a causal relationship to the vaccine.

What to do if someone has a reaction to a vaccine?

If you have any concerns about potential side effects of vaccines, talk to your doctor or nurse. In general, most children who have had a reaction to a vaccination can be safely re-vaccinated. Speak to your doctor for further advice.

What are the adverse events of immunizations?

Pain, redness, or swelling where the shot was given, mild fever, headache, feeling tired, and nausea, vomiting, diarrhea, or stomachache sometimes happen after Td vaccination.

For pdfFiller’s FAQs

What is REPORT OF ADVERSE EVENTS FOLLOWING IMMUNIZATION (AEFI)?

The Report of Adverse Events Following Immunization (AEFI) is a documentation process used to record any unexpected or harmful reactions that occur after vaccination. It helps in monitoring vaccine safety and efficacy.

Who is required to file REPORT OF ADVERSE EVENTS FOLLOWING IMMUNIZATION (AEFI)?

Healthcare providers, including doctors and nurses, as well as individuals receiving the vaccine, parents, or guardians of minors, are typically required to file reports of adverse events following immunization.

How to fill out REPORT OF ADVERSE EVENTS FOLLOWING IMMUNIZATION (AEFI)?

To fill out the AEFI report, obtain the appropriate form from the local health authority or government website, complete it with details regarding the adverse event, vaccination details, patient demographics, and any other pertinent medical information, and submit it to the designated health authority.

What is the purpose of REPORT OF ADVERSE EVENTS FOLLOWING IMMUNIZATION (AEFI)?

The purpose of the AEFI report is to ensure the ongoing safety of vaccines by systematically tracking and analyzing adverse events, thus helping public health authorities make informed decisions regarding vaccine use and safety.

What information must be reported on REPORT OF ADVERSE EVENTS FOLLOWING IMMUNIZATION (AEFI)?

The information required on an AEFI report typically includes the patient's demographic data, details about the vaccine administered, description of the adverse event, timing of the event relative to vaccination, and any other relevant medical history or interventions.