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HOME / PHARMACOVIGILANCE

Patient safety is our priority.

ADVERSE EVENT / SIDE EFFECT REPORTING

A robust approach to medicine safety

Pharmacovigilance is the science of understanding, monitoring and assessing possible medicine-related problems that may occur with consumption or application.

Who can report?

Anyone can report an adverse event or suspected side effect associated with a medicine.

What should be reported?

  • All suspected adverse events or side effects
  • Overdose or accidental use
  • Medication errors
  • Abuse and misuse
  • Pregnancy or breastfeeding exposure
  • Drug interactions
  • Occupational exposure
  • Lack of efficacy
  • Unexpected clinical benefit
  • Use in an unapproved indication

Adverse Drug Reaction Reporting Form

Download the form, complete the available details and share it with our pharmacovigilance team.

RESPONSIBLE REPORTING

How we manage safety information

Neeupure Pharma Pvt. Ltd., as a responsible marketer of pharmaceutical products, has designed a complaint-handling system integrated with its quality system to manage reports swiftly and effectively in accordance with applicable guidelines.

We understand the importance of monitoring drug safety and strive to support safe and rational use of medicines. Please provide as much information as possible; however, do not delay reporting if all details are not available.

Contact Our Team