Pharmacovigilance

Pharmacovigilance - Pharmacovigilance is the scientific and systematic process of monitoring, assessing, detecting, and preventing adverse effects or any other drug-related problems, primarily focusing on the safety of pharmaceutical products after they have been released on the market. It aims to enhance patient care and safety in relation to the use of medicines and to support public health programs by providing reliable, balanced information for the effective assessment of the risk-benefit profile of medicinal products.

Class Information

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Identification

IRI: https://folio.openlegalstandard.org/RDTRvcsDvO0p9ngadut1B5j
Label (rdfs): Pharmacovigilance
Preferred Label: None
Alternative Labels: Drug Safety Monitoring, Post-Market Surveillance
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Definition and Examples

Definition: Pharmacovigilance is the scientific and systematic process of monitoring, assessing, detecting, and preventing adverse effects or any other drug-related problems, primarily focusing on the safety of pharmaceutical products after they have been released on the market. It aims to enhance patient care and safety in relation to the use of medicines and to support public health programs by providing reliable, balanced information for the effective assessment of the risk-benefit profile of medicinal products.
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Class Relationships

Sub Class Of: Health Regulatory Events
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Additional Information

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Deprecated: False

Metadata

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