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Report an Adverse Event

Patient Safety Comes First

Report a suspected side effect or product-quality concern involving a Kaizen Pharmaceuticals medicine.

Medical emergency? Contact a healthcare professional or emergency services immediately. Do not wait to submit a report.

Pharmacovigilance

Monitoring Medicine Safety

Pharmacovigilance is the science of detecting, assessing and preventing adverse effects and other medicine-related problems. At Kaizen Pharmaceuticals, we continuously monitor the safety and quality of our medicines throughout their lifecycle.

Every report helps build a clearer picture of how medicines perform in real use and supports safer treatment decisions.

What to Report

If in Doubt, Report It

An adverse event is any unwanted or unexpected medical occurrence after using a medicine. It does not necessarily mean the medicine caused it, so please report even if you are unsure.

Side effects or adverse reactions Serious or unexpected events Overdose or medication errors Use in pregnancy or breastfeeding Misuse, abuse or off-label use Suspected drug interactions Lack of expected effect Accidental or occupational exposure
Anyone Can Report

What We Need From You

Patients, caregivers, healthcare professionals, institutions and partners can all submit a report. Share as much as you can. Incomplete information should never stop you from reporting, and our team may follow up for details.

01

Patient

Initials, age or gender

02

Reporter

Your name and contact details

03

Product

Name or active ingredient

Adverse Event

Report a Suspected Adverse Event

Use our online Adverse Drug Reaction (ADR) form to tell us about the patient, the medicine and what happened.

Product Quality

Report a Product Quality Complaint

For concerns with packaging, labelling, appearance, performance or authenticity, such as a broken seal, damaged tablets or a suspected counterfeit.

Privacy and Confidentiality

Your Information Is Protected

Reports are used only for drug safety, product quality, regulatory reporting and follow-up. Personal information is handled securely and shared only where required, in line with applicable laws and pharmacovigilance requirements.