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.
