Reporting Adverse Event and Quality Defect

A service that allows you to report adverse events, medication errors, and product quality defects of BPharma Products.

What is Pharmacovigilance ?

Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other medicine/vaccine related problem.

What is Adverse Event ?

Defined as a response to a medicinal product, which is noxious and unintended.

What is Quality Defect ?

Defined as any difference in the appearance, physical-chemical, microbiological and pharmaceutical-technological properties of the actual situation of medicinal product and information from marketing authorization.

Why do we report Adverse Event ?

BPharma maintains active surveillance to ensure the safety of our patients and that our products have a complete safe profile. Your information will allow us to take the necessary action to increase the safety of the BPharma produ

If you experienced adverse event or found a quality defect while using any of our products, please fill the below report form.

By providing any side effects related to BPharma products, you help us to ensure the safety of our products and our patients. Your information will enable us to fulfill its reporting responsibility to health authorities and to undertake necessary investigations.

Adverse Drug Reaction (ADR) Reporting Form

Patient Information

Product Information

Description of the Adverse Event

Reporter Details (Only for Health Care Providers)