Adverse Drug Reaction (ADR) Reporting

Dedication to Patient Safety

Pharmacovigilance at Supernova is a proactive and essential process focused on the continuous oversight of our medications once they are in clinical use. By systematically tracking and analyzing unexpected side effects, we strive to ensure that all treatments prioritize patient health and minimize potential risks. This rigorous safety monitoring is fundamental to our mission of promoting the responsible use of pharmaceutical solutions worldwide.

The Supernova Commitment

At Supernova, we are deeply committed to our drug safety responsibilities. We encourage healthcare professionals, patients, and all concerned parties to report any complications or adverse events associated with the administration of our products. These insights allow our team to perform ongoing assessments of the benefit-risk ratio, ensuring that every Supernova drug continues to meet the highest standards of safety and efficacy.

Reporting and Support

If you encounter a suspected adverse reaction or a safety-related issue, please report it immediately to help us maintain the highest level of care. You can submit your report officially through our digital system by using the Adverse Drug Event Reporting Form:

You may also contact our dedicated safety and quality assurance team directly via the representatives listed below:

Dr. Alok Kumar

Technical Director

9958881747

Mr. Prashant Yadav

Q.A. Manager

8894001755

Mr. Charan Singh

Sr. Executive

8688040004

NameDesignationContact No.
Dr. Alok KumarTechnical Director9958881747
Mr. Prashant YadavQ.A. Manager8894001755
Mr. Charan SinghSr. Executive8688040004