Pharmacovigilance or drug safety in lay man language. Pharmacovigilance is the science that connects to the detection, collection, monitoring, assessment, and prevention of the negative effects of pharmaceutical products. Pharmaceutical vigilance mainly involves the evaluation of information and facts provided by the health care providers. Pharmacovigilance excessively focuses on the adverse reactions of drugs, defined as the response to an unintended and noxious drug. It also includes the inefficiency of the drug. Errors like abuse and overdose of the medication and drug exposure during pregnancy despite the lack of an adverse effect are considered to result in an adverse drug reaction.
These stages include:
Pharmacovigilance Detection Process:
Pharmacovigilance Assessment Process:
Closure of the case:Best Clinical Research Course.
Understanding and Analysing the Drug safety profile:
Prevention of the negative effects:
Collaboration in the field of pharmacovigilance forms the foundation of the WHO program for international drug monitoring. These reports are generally analyzed locally and could lead to action within the country itself. The WHO program membership of any country helps them keep up with similar researches and reports that are made worldwide. When there are multiple reports of a particular drug, this process may lead to a detection of a signal which could be hazardous to the human body.
Ecopharmocovigilance: pharmacovigilance courses