Bestel Lab

Pharmacovigilance & Patient Safety

Committed to Your Well-being

At Bestel Laboratories Private Limited, patient safety is our highest priority. Our Pharmacovigilance department is dedicated to the continuous monitoring, assessment, and prevention of adverse effects or any other drug-related problems. By maintaining a rigorous safety surveillance system, we ensure that the benefits of our medicines continue to outweigh the risks across all therapeutic segments—from Gynaecology to Neurology.

If you have experienced a side effect or adverse reaction related to any Bestel Laboratories product, we encourage you to report it to us immediately. Your feedback helps us improve patient safety for everyone.

How to Report: You can report safety information through any of the following channels:

Email

safety@bestellaboratories.com

Phone/Helpline

+91-2692319243

Postal Address

Pharmacovigilance Department, Bestel Laboratories Pvt. Ltd., Anand, Gujarat, India.

Note to Patients: Please consult your healthcare provider or physician for medical advice regarding side effects. Our Pharmacovigilance team cannot provide medical treatment or individual prescriptions.

Information Needed for Reporting

To help our safety team investigate thoroughly, please try to provide the following details when you contact us:

  1. Patient Details:(Initials, age, or gender).
  2. Product Name:The name of the Bestel medication used.
  3. Description of the Event:A brief explanation of the side effect experienced.
  4. Reporter Details:Your name and contact information (for follow-up purposes).

Frequently Asked Questions (FAQ)

What is Pharmacovigilance?

It is the science and activities relating to the detection, assessment, understanding, and prevention of adverse effects or any other medicine-related problems.

Why should I report a side effect?

Reporting side effects helps us identify rare reactions that may not have been seen in early clinical trials, making medicines safer for all patients in the future.

Is my data private?

Yes. All personal information shared for pharmacovigilance purposes is kept strictly confidential and used only for safety evaluation in accordance with data privacy laws.

Adverse Event / Side Effect Reporting Form

    Date of Event Onset
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