Pharmacovigilance Policy

NIXI LABORATORIES PVT. LTD.

At Nixi Laboratories Pvt. Ltd., the safety of our patients and healthcare professionals (HCPs) is of the utmost importance. We are committed to ensuring that our products meet the highest standards of quality, efficacy, and safety. To maintain transparency and safeguard public health, we have developed a robust Pharmacovigilance system to monitor, assess, and respond to adverse events associated with our products.

What is Pharmacovigilance?

Pharmacovigilance (PV) refers to the science and activities related to detecting, assessing, understanding, and preventing adverse effects or any other drug-related problems. It plays a crucial role in ensuring that Nixi Laboratories Pvt. Ltd. products are safe for use by continuously monitoring and evaluating any reported issues.

Reporting Adverse Events

We encourage all healthcare professionals and patients to report any adverse events or side effects they may experience while using Nixi Laboratories Pvt. Ltd. products. Your reports contribute to improving the safety of medications and help us take immediate action to prevent further risks.

Who Can Report?

• Healthcare Professionals (Doctors, Nurses, Pharmacists, etc.)
• Patients and Caregivers
• Hospital Authorities

What to Report?

Please report any of the following related to Nixi Laboratories Pvt. Ltd. products:

• Side effects or unexpected adverse reactions
• Lack of expected drug efficacy
• Medication errors
• Drug interactions
• Any other unusual effects related to product use

How to Report an Adverse Event?

You can report any adverse events related to Nixi Laboratories Pvt. Ltd. products through the following methods:

• 1. Email

Send your report directly to our Pharmacovigilance Department at: pv@nixilaboratories.com

Kindly include the following details:

• Product name
• Batch number (if available)
• Description of the event
• Patient details (age, gender, etc.)
• Contact details (for follow-up, if needed)

• 2. Contact Number

For immediate reporting or to speak to our Pharmacovigilance experts, call our toll-free numbers: 7807888710, 9816143310

• 3. Postal Mail

You may also send your adverse event report to:


NIXI LABORATORIES PVT. LTD.
Pharmacovigilance Department
VPO: Mouza Ogli, Sadhaura Road , Kala Amb
District Sirmour, H.P.

Why Your Report Matters

Your contribution is vital for improving drug safety and ensuring better outcomes for all patients. Every report helps us enhance our understanding of product safety profiles and take necessary actions to protect public health.

National ADR Reporting

For more detailed information about adverse drug reactions (ADRs) and to report ADRs using official forms, you may also visit the Pharmacovigilance Programme of India (PvPI) website. The PvPI provides access to downloadable ADR reporting forms for both healthcare professionals and patients.
Visit: https://www.ipc.gov.in/PvPI/adr.html

Together, let us ensure patient safety and continuous monitoring of medication effects for a safer healthcare system.