Safety & Adverse Event Reporting – Jenner Pharmaceuticals

What Is an Adverse Event?

An adverse event is any unwanted or unexpected reaction experienced after taking a medicine. This may include:

Side effects.
Allergic reactions.
Lack of expected effect.
Medication errors.
Product quality concerns.
Not all adverse events are serious, but all reports are important.

Who Can Report an Adverse Event

Adverse events may be reported by:
Patients or caregivers.
Doctors, pharmacists, and nurses.
Other healthcare professionals.
You do not need to be certain that the medicine caused the event in order to report it.

When Should You Report

You experience a reaction you were not expecting.
A side effect becomes bothersome or severe.
A medicine does not appear to work as expected.
There is a concern about product quality.
In medical emergencies, seek immediate medical attention before reporting.

How to Report an Adverse Event

Reports can be submitted through the following channels:

Online Reporting

Complete the adverse event reporting form available on this website.

What Happens After You Report

All reports are reviewed by qualified pharmacovigilance personnel.

Information is handled confidentially.

Reports are evaluated and, where required, shared with regulatory authorities in accordance with local regulations.

Reporting an adverse event does not replace medical care or advice.

Data Privacy & Confidentiality

Information collected through adverse event reporting is used solely for safety monitoring purposes and handled in accordance with applicable data protection laws.