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LIFESPARK Pharma Private Limited

Report a Side Effect or Product Complaint

If a LifeSpark product caused an unexpected effect, or a pack was not as it should be, please tell us. Reports are read by our pharmacovigilance team, not by sales.

  • Acknowledgement · within 48 hours We confirm receipt of every report, with a reference number, within this time.
  • Serious events · within 24 hours A report marked serious is escalated to the pharmacovigilance officer within this time.
  • Substantive reply · within 15 days We come back with the outcome of our assessment, or tell you what is still outstanding.

Report form

Fields marked * are required. Tell us as much as you can remember — an incomplete report is far better than no report.

What are you reporting?
We send your reference number here.
Useful if we need to ask a follow-up question.
Printed on the carton, usually next to the expiry date.
This report goes to the pharmacovigilance team, not to sales.

What happens after you submit

  1. 1

    Logged

    Immediately

    Your report is recorded with a unique reference and routed to pharmacovigilance, not to sales.

  2. 2

    Acknowledged

    Within 48 hours

    We confirm receipt in writing and tell you if we need anything further.

  3. 3

    Assessed

    Ongoing

    We check the batch record and release data, and assess whether the product is likely to be related.

  4. 4

    Answered

    Within 15 days

    You receive the outcome. Where required, the event is also reported to the regulatory authority.

You may also report a suspected adverse drug reaction directly to the national Pharmacovigilance Programme of India, independently of us. Reporting to us does not replace that right, and we would rather you reported an event twice than not at all.