Drug Safety Journals
Pharmacovigilance is defined because the science and activities concerned with the detection, assessment, understanding and prevention of adverse reactions to medicines (i.e.
adverse drug reactions or ADRs). The last word goal of this activity is to enhance the safe and rational use of medicines, there by improving patient care and public health. Drug safety and
pharmacovigilance remains a dynamic clinical and science .
Pharmacovigilance is defined by the World
Health Organization (WHO) as ’the science and activities concerning the detection, assessment, understanding and prevention of adverse effects or the other drug-related problem’; it plays an important role in ensuring that doctors, along side the patient, have enough
information to form a choice when it involves choosing a drug for treatment. However, despite all their benefits, evidence continues to urge those bigger adverse reactions to medicines which are common, yet often preventable, explanation for illness, disability and even death. In some countries,
adverse drug reactions (ADRs) rank among the highest 10 leading causes of mortality. In order to stop or to scale back harm to patients and thus improve public health, mechanisms for evaluating and monitoring the security of medicines in clinical use are vital.
Pharmacovigilance programs within the next 10 years, describe in short the potential implications of such trends on the
evolution of the science.
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