Pharmacovigilance Department

The objective of pharmacovigilance is to safeguard public health by ensuring the safety, efficacy, and quality of medicinal products. The pharmacovigilance system is aimed at the early detection of adverse drug reactions and the minimization of associated risks.

Tasks of the Pharmacovigilance Department

  • Conducting pharmacovigilance activities.
  • Ensuring the evaluation of pharmacovigilance system documentation at the stage of medicinal product registration and renewal of the registration certificate.
  • Ensuring the assessment of Periodic Safety Update Reports (PSURs) during the post-registration period of medicinal products in accordance with the legislation of the Republic of Uzbekistan.
  • Entering all cases of adverse drug reactions related to medicinal products, reported by healthcare institutions, pharmacies, and organizations manufacturing, distributing or using medicinal products, into the pharmacovigilance database via email farmakonadzor@ssv.uz, pharmcompv@gmail.com and through the Telegram bot @uzpharmcontrolbot.
  • Monitoring adverse drug reactions and developing specific measures for their prevention or mitigation, including recommendations for withdrawal from medical practice.
  • Collecting all reports on adverse effects associated with medicinal product use, assessing them based on follow-up data, ensuring proper evaluation of report quality, and verifying the accuracy, reliability, and completeness of data for clinical assessment.

See also other products:


See also:


See also other state duties:


See also:


See also departments:




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