[Post-licensure safety surveillance for influenza A(H1N1) pandemic vaccines: first results]

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Alexis Jacquet1, Shéhérazade Ouaret, Carmen Kreft-Jaïs

  • 1Département de pharmacovigilance, Agence française de sécurité sanitaire des produits de santé, 93000 Saint-Denis. alexis.jacquet@afssaps.sante.fr

La Revue Du Praticien
|March 24, 2011
PubMed
Abstract

No abstract available in PubMed .

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Pharmacovigilance01:19

Pharmacovigilance

Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a drug is widely used over an extended period.
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
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Influenza

Influenza is an acute, highly communicable viral disease that affects the respiratory tract and is responsible for seasonal epidemics worldwide. Influenza A is the most prevalent type associated with widespread outbreaks and is subtyped based on two surface glycoproteins: hemagglutinin (H) and neuraminidase (N), as in H1N1. These glycoproteins are essential for viral infectivity, transmission, and immune recognition. Transmission occurs primarily through respiratory droplets and contaminated...
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