
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
| Name | Designation | Contact No. |
|---|---|---|
| Dr. Alok Kumar | Technical Director | 9958881747 |
| Mr. Prashant Yadav | Q.A. Manager | 8894001755 |
| Mr. Charan Singh | Sr. Executive | 8688040004 |

