Drug Safety – Adverse Event Reporting
Tanishka Pharmaceuticals is committed to ensuring the safety and effectiveness of all its products. If you wish to report an adverse event associated with any of our manufactured products, please complete the Adverse Event Reporting Form and email it to our Quality Assurance team.
Report an Adverse Event
What is an Adverse Event?
An adverse event is any undesirable experience associated with the use of a medicinal product in a patient. It is commonly referred to as a side effect.
Why Should I Report an Adverse Event?
Reporting adverse events helps us collect important safety information and improve the safe use of medicines. Your report may assist in identifying:
- Rare adverse effects
- Unexpected or previously unknown adverse effects
- Drug–drug and drug–food interactions
- Unknown risk factors
- Long-term safety concerns
This information plays a vital role in protecting public health by helping identify, assess and manage medicine-related risks effectively.
What Should Be Reported?
Please report any suspected adverse event or side effect occurring after the administration of any product manufactured by Tanishka Pharmaceuticals.
Where Should I Report It?
Email your completed report to:
qc.tanishkapharma@gmail.com
qatanishka@gmail.com
Confidentiality
The identity of the patient and reporter will be treated with the strictest confidence and protected to the fullest extent permitted by law. Tanishka Pharmaceuticals will not disclose the reporter’s identity in response to public requests.