Adverse Event Reporting

Adverse drug reaction is defined as any response to a drug which is noxious and unintended, and which occurs at doses normally used in human for prophylaxis, diagnosis, or therapy of disease, or for the modification of physiological function.

• 'Any adverse experience / side effect’ experienced after taking/adminstering Pharmazz medicine(s): Consumer, Caregiver, Healthcare professionals can report.
• Besides, these are other scenarios/ situations (cited below as examples) which can be reported to Pharmazz, Pharmacovigilance department for any Pharmazz drug that is in question.
• Pharmazz drug was given to or taking by pregnant patient → Report to Pharmacovigilance department as pregnancy exposure.
• Pharmazz drug didn’t work → Report to Pharmacovigilance department as Lack of efficacy.
• Overdose of Pharmazz drug was given to or taking by patient → Report to Pharmacovigilance department as overdose.
• Pack of Pharmazz drugs that are discoloured, or damaged → Report as Product Complaint.
• Adverse Event is already available within the product package insert – would you still report this? → Report everything to Pharmacovigilance department.
• If an adverse event by Pharmazz drug is reported to you as the company representative, but no trade name is given → Report everything to Pharmacovigilance department.

Any health care professional (Doctors, Dentists, Nurses, Pharmacists etc.)

Non healthcare professional (Patient, caregiver, friend, etc.)

Confidentiality:

The patient's identity is held in strict confidence and protected to the fullest extent. Pharmazz shall not disclose the reporter’s identity in response to a request from the public.