During the clinical trials of an investigational drug, timely evaluation of safety data is crucial to the ongoing assessment of risk to trial subjects. It is also important to inform…

Pharmaceutical legislation provides a legal framework, to ensure the availability of acceptably safe, effective enhancement and high-quality medicines to patients. Within this framework, marketing authorization holders (MAHs) are requested to…

Pharmacovigilance is an essential component of pharmaceutical safety [1]. The United Journal of Pharmacovigilance opens a new space for the dissemination of scientific data in this area of research, based…

Pharmacovigilance plays a major role before and after the drug development process. In this article, a detailed explanation of the pharmacovigilance actives and the benefit-risk evaluation has been discussed. Every…

It is well known that prescription drugs can result in a myriad of ADRs, including psychiatric ADRs. Psychiatric effects of drugs can impact sensorium, attention, concentration, memory, and higher cognitive…