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National Pharmacovigilance Centre, DRAP collects reports of suspected Adverse Events associated with the use of therapeutic products. Anyone can report a suspected adverse events.
DRAP has enabled both electronic and manual systems for collection of reports of suspected adverse events:-
LEARNING OBJECTIVES
Define an adverse drug reaction.
Discuss the detection of adverse drug reactions.
Discuss the assessment of adverse drug reactions.
WHAT HAPPENS TO THE REPORT?
Your report matters. Together, letus save lives through vigilant reporting.
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