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Comprehensive Evaluation of the Effectiveness and Safety of Placenta-Targeted Drug Delivery Using Three Complementary Methods
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Estudio de vigilancia posterior a la comercialización de Norplant en países en desarrollo

P Hannaford1

  • 1Department of General Practice and Primary Care, University of Aberdeen, Foresterhill Health Centre, AB25 2AY, Aberdeen, UK. p.hannaford@abdn.ac.uk

Lancet (London, England)
|June 19, 2001
PubMed
Resumen

No abstract available in PubMed .

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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.
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