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 ?

Please download the AER form from here, fill it with the required details and send it to :
Pharmacovigilance Dept. (V.P – QA and Regulatory Affairs)
Naxpar Pharma Pvt. Ltd.
104, Bldg. No.8,
Jogani Industrial Estate,
Chunabhatti, Sion,
Mumbai – 400022
Download AER Form

Or scan and email it to

Contact :
Kindly call +91-1795-248666 and request to connect to “Pharmacovigilance Dept.” and you will be routed to the concerned person with whom you can share your experience.