Pharmaceutical Adverse Event Reporting Checklist

Ensure accurate and compliant adverse event reporting with our Pharmaceutical Adverse Event Reporting Checklist. Streamline your processes, minimize risk, and maintain regulatory adherence-because patient safety is paramount.

This Template was installed 5 times.

Event Identification & Initial Assessment

1 of 10

Gather initial information about the adverse event and determine its potential severity.

Date of Event Occurrence

Time of Event Occurrence

Brief Summary of the Event

Initial Severity Assessment

Patient Age (years)

Reporting Source

Patient Information Verification

2 of 10

Confirm patient identity and relevant medical history.

Patient Full Name

Date of Birth (YYYY-MM-DD)

Patient Medical Record Number

Gender

Relevant Medical History (Brief Summary)

Patient Contact Method Preference

Product Information Confirmation

3 of 10

Verify the specific pharmaceutical product involved and lot number.

Drug Name

Lot Number

Expiration Date (YYMMDD)

Quantity Administered

Dosage Form

Product Packaging Photo (if available)

Event Description and Timeline

4 of 10

Document detailed information about the event, including onset, duration, and resolution (if applicable).

Detailed Description of Adverse Event

Date of Event Onset

Time of Event Onset

Date of Event Resolution (if applicable)

Time of Event Resolution (if applicable)

Duration of Event (in hours/minutes)

Sequence of Events Leading Up to the Adverse Reaction

Severity of Event (e.g., Mild, Moderate, Severe)

Medical Intervention & Outcome

5 of 10

Record any medical interventions performed and the patient's response.

Describe the medical interventions performed (e.g., medications, procedures).

Dosage of medication administered (if applicable).

Date of intervention.

Time of intervention.

Describe the patient's immediate response to the intervention.

Overall Outcome of Intervention

Describe any long-term effects or sequelae observed.

Physician/Healthcare Provider Confirmation

6 of 10

Obtain confirmation and supporting documentation from the treating physician or healthcare provider.

Physician/Healthcare Provider Signature

Date of Confirmation

Physician/Healthcare Provider Name

Physician/Healthcare Provider Credentials

Summary of Physician Assessment (e.g., Causality Assessment, Severity)

Causality Assessment (e.g., Definite, Probable, Possible, Unlikely, Not Related)

Severity Score (if applicable, per internal scoring system)

Regulatory Reporting Requirements

7 of 10

Determine applicable reporting requirements (e.g., FDA, EMA).

Reporting Jurisdiction

Reporting Form Type

Specific Regulatory Guidelines Applied

Reporting Deadline (Days)

Submission Date

Supporting Documentation (Regulatory)

Internal Reporting and Documentation

8 of 10

Complete necessary internal forms and enter data into relevant systems.

Case/Incident ID

Date of Internal Report

Summary of Adverse Event (for internal records)

Severity Assessment (Internal)

Affected Departments

Supporting Internal Documents (e.g., lab reports)

Internal Notes/Comments

Review and Approval

9 of 10

Ensure accuracy and completeness of the report before submission.

Reviewer Signature

Review Date

Review Outcome

Reviewer Comments (if applicable)

Revision Count (if applicable)

Submission and Tracking

10 of 10

Submit the report to the appropriate regulatory agency and track its status.

Submission Date

Submission Time

Submission Method

Tracking Number (if applicable)

Confirmation Code (if applicable)

Notes on Submission (e.g., communication with agency)

Submission Status

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