Pharmacovigilance

Pharmacovigilance at Bistra

At Bistra, we place patient safety and medication effectiveness at the heart of everything we do. Our Pharmacovigilance system is dedicated to monitoring and evaluating the safety of all our pharmaceutical or food or cosmetic products as per local regulatory meeting regulatory compliance. Your feedback is invaluable in helping us identify any potential risks and ensuring the highest standards of patient care.

Why Report Adverse Drug Reactions (ADRs)?

Protect Others: Reporting any unexpected side effects helps us identify safety concerns early.
Improve Products: Your input supports ongoing evaluation and optimization of our medicines.
Enhance Knowledge: Aggregated data allows our experts and healthcare authorities to better understand how drugs behave in real‑world use.

How to Report an Adverse Drug Reaction

If you or someone you care for experiences an adverse effect or any safety concern related to one of our products, please let us know.

Download the ADR Reporting Form
Click the button below to download our standardized Adverse Drug Reaction form:

In addition to reporting directly to Bistra Scientific, you can also contact one of Nepal’s 19 designated Regional Pharmacovigilance Centres to report any Adverse Drug Reactions (ADRs) or medication safety issues.

These centres work in collaboration with the Department of Drug Administration (DDA), Nepal to strengthen drug safety and ensure patient well-being nationwide.