Centre ties up with 3 states to boost drug safety, adverse reaction reporting

In a move aimed at strengthening medicine safety and improving monitoring of adverse drug reactions, the Indian Pharmacopoeia ...
The Nation Newspaper

NAFDAC decries low report of adverse drug effect in 2016

The Acting Director General of the National Agency For Food and Drug Administration and Control, Mrs. Yetunde Oni, has decried the low rate of response to Adverse Drugs Reaction (ADR) Mrs. Oni said ...

Tragic death leads to call for mandatory drug reaction reports

The death of a Creston woman from a fatal interaction between two prescription drugs has led to a call from the B.C. Health Professions Review Board for mandatory reporting of adverse drug reactions.
RAPS

FDA consolidates adverse events reporting systems

The US Food and Drug Administration (FDA) announced it is unifying its various adverse reporting systems into a single system called the Adverse Event Monitoring System (AEMS). The agency said the ...