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 patientsafety@naxparlab.com
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.