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There are three methods for reporting pharmacovigilance activities (see figure below).

 

Figure: Three Methods for Reporting Pharmacovigilance Activities

 

 

  1. Spontaneous Reporting
    • Spontaneous (or voluntary) reporting means that no active measures are taken to look for adverse effects other than the encouragement of health professionals and others to report safety concerns.
    • Reporting is entirely dependent on the initiative and motivation of the potential reporters.
    • This is the most common form of pharmacovigilance, sometimes termed passive reporting.
    • In some countries this form of reporting is mandatory.
    • Clinicians, pharmacists and community members should be trained on how, when, what and where to report.
  2. Targeted Reporting
    • It focuses on capturing Adverse Drug Reactions (ADRs) in a well-defined group of patients on treatment. 
    • Health professionals in charge of the patients are sensitized to report specific safety concerns.
  3.  Active Surveillance
    • It is a proactive effort made to elicit adverse events.
    • This is achieved by active follow-up after treatment and the events may be detected by asking patients directly or screening patient records. 
    • It is best done prospectively.
    • The most comprehensive method of active surveillance is Cohort Event Monitoring (CEM), which is an adaptable and powerful method of getting good comprehensive data.
    • Other methods of active monitoring include the use of registers, record linkage and screening of laboratory results in medical laboratories.
    • This is an important method of reporting under active Drug Safety Monitoring (aDSM) for Drug-resistant TB (DR-TB) patients.

 

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