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Adverse Event Reporting

Precise Group has a strong commitment towards manufacturing quality products. The safety of pharmaceutical product may not be distinct, post effects of drug when used in combination of other drugs are generally unknown and safety concerned in different groups can be different as in young children, elderly patient, pregnant women. Therefore to monitor the safety of its product when the product is available for clinical practice, Precise Group has moral and regulatory responsibility to conduct Pharmacovigilance activities.

Precise Group has a pharmacovigilance system to safeguard patient health through efficient and timely identification, collection, assessment, and communication of medicine-related adverse events.


What is Pharmacovigilance


Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of side effects or any other possible drug related problems.

Aim of Pharmacovigilance:

The specific aims of Pharmacovigilance are to

  • Improve patient care and safety

  • Contribute to the assessment of benefit-risk ratio of medicines, encourage safe, effective and rational use of medicines

  • Promote understanding, education and clinical training in pharmacovigilance and its effective communication to the public.

An adverse event is any untoward medical occurrence in a patient following administration of a pharmaceutical product and which does not necessarily have a causal relationship with the administered product. If you wish to report a suspected adverse reaction/side effect occurred with our drug, you can do so by choosing any of the following options:

  • Complete and submit the ADR Reporting form online available on this website

  • If you would like to send us information by post or email, please download the form here and mail to the address mentioned in footer.

  • If you use email please write reporting adverse event in the email header and send to

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