What is an Adverse Event (AE)

An adverse event (AE) is any unintended medical occurrence in a patient or clinical trial participant who has been given a pharmaceutical product, supplement, medical device, or treatment-regardless of whether it is causally related to that product or treatment.

Malaysia

Adverse Event Reporting
Product Inquiry / Complaint

Singapore

Adverse Event Reporting
Product Inquiry / Complaint

Adverse Event Report & Product Feedback Form

Pharm-D is committed to ensuring the safety and quality of our products. If you have experienced an adverse event, have a product-related enquiry, or wish to report a complaint, please complete the form below.

  • Healthcare professionals
  • Patients or caregivers
  • Distributors and partners

Your report helps us monitor product performance and take appropriate action where necessary.


    What Happens Next?

    Once submitted, our Regulatory/ Quality/ Pharmacovigilance team will review your report. You may be contacted for additional information. We aim to respond within 3 working days.


      What Happens Next?

      Once submitted, our Regulatory/ Quality/ Pharmacovigilance team will review your report. You may be contacted for additional information. We aim to respond within 3 working days.