https://doi.org/10.36719/2663-4619/112/111-118
Sakit Atakishiyev
Azerbaijan State Agrarian University
https://orcid.org/0009-0009-8261-8245
sakit.atakishiyev@adau.edu.az
Aybaniz Taghizadeh
Azerbaijan State Agrarian University
https://orcid.org/0009-0005-7277-662X
aybaniz.tagizada@adau.edu.az
Oktay Aliyev
Azerbaijan State Agrarian University
https://orcid.org/0009-0003-9281-8976
oktay.aliyev@adau.edu.az
Aytakin Mammadova
Azerbaijan State Agrarian University
https://orcid.org/0000-0001-5834-2546
aytakin.mammadova@adau.edu.az
General Information About Pharmacovigilance
Abstract
Pharmacovigilance is a systematic process that ensures the monitoring of the safety and efficacy of medicines. It is of great importance to ensure the public's access to safe and effective medicines, as well as to ensure that manufacturers make decisions based on scientific and ethical principles when developing and marketing pharmaceutical products. Pharmacovigilance is a set of scientific and regulatory activities that monitor the safe use of medicines and detect, evaluate, analyze, and prevent their potential risks. The implementation of pharmacovigilance systems is of great importance in ensuring the safety of medicines and protecting public health. This field includes the investigation of side effects and other possible pharmacological problems associated with the use of medicines.
Keywords: pharmacovigilance, drug, risk, side effect, safety