Naxpar Group is strongly committed to manufacturing and providing quality products. However all pharmacologically effective drugs have their benefits and their risks. Naxpar Group would like to hear from you incase of any comprehensive adverse reactions if any.
Based on your submission, it will help in continuous monitoring of the safety of a drug throughout the duration of its use which will help to ensure that its risks and benefits are acceptable.
What is an Adverse Event ?
Adverse Event is defined as an undesirable medical condition that can be symptoms, signs or any abnormal results of an investigation. Adverse Events are not necessarily caused by the medication – the event just needs to have occurred after taking a medication in question.
What to report ?
Customers, Patients, Users or Healthcare Professionals can report any adverse experience noticed or diagnosed after consumption / application of products manufactured by the Naxpar Group.
Where to report ?
Option 1
Please download the AER form from here or by clicking the “Download AER Form” button below.
fill the form with the relevant details and post/courier it to :
Pharmacovigilance Dept. (Q.A / Q.C) c/o Naxpar Pharma Pvt. Ltd.
182, Vill. Gurumajra, Kishanpura,
Tehsil Baddi, Dist. Solan,
H.P – 174101
Download AER Form
Option 2
Scan and Email the AER Form to patientsafety@naxparlab.com
Option 3
Contact via Telephone Call :
Kindly call +91-1795-352600 and ask to be forwarded to “Pharmacovigilance Dept.” and you will be routed to the concerned person with whom you can share your experience or feedback.