Report a side effect or adverse event

Patient safety depends on every event being reported — even if you're not sure it's related to the medicine. Please share as much detail as you can. Your information is kept confidential and reported to the regulator as required under Indian law.

Reporter details

I am a

Your name

Phone

Patient details (de-identified)

Patient initials (optional)

Age / age range

Sex

Product & event

Saneveda product

Batch number (from pack)

Date the event started

Describe what happened

Outcome

I consent to Saneveda Healthcare processing this information for pharmacovigilance purposes in line with Indian regulations and the company's Privacy Policy.

Thank you — your report has been received.

You'll get an acknowledgement email with a reference number within 1 working day. Our pharmacovigilance officer will follow up within 3 working days.

This form is a V1 placeholder and does not yet send data to a server. For urgent reports, please call or email the pharmacovigilance officer.

Pharmacovigilance Officer

For urgent safety reports, contact our PV officer directly.

+91 8884 739 956
PV hours: 9 am – 6 pm IST, Mon–Sat

pv@sanevedahealthcare.in

You can also report to the regulator

Adverse events can be reported directly to the Pharmacovigilance Programme of India (PvPI), run by the Indian Pharmacopoeia Commission (IPC) under CDSCO, via the national toll-free helpline 1800-180-3024 (Mon–Fri, 9 am–5:30 pm IST), by email to pvpi.ipc@gov.in, or through the “ADR PvPI” mobile app (Android). Forms and details are at ipc.gov.in.

An adverse event is any undesirable experience associated with the use of a medicine — whether or not it is considered related to the medicine. When in doubt, please report it.