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We have discussed the vital role that
spontaneous reporting plays in post-market/post-approval
pharmacovigilance. Patient (consumer) and health care provider
(HCP) reporting of potential adverse drug reactions and the
subsequent medical adjudication and data-basing of this information
into systems such as FDA’s FAERS and UMC’s Vigibase databases forms
the backbone of how we continue to develop the safety profile and
benefit: risk profile of approved drugs/biologics.
A unique part of the world we live in today is the ubiquity
of social media. Facebook. Instagram. Twitter. We have so many
tools at our fingertips for expressing our opinions to a large
audience. And naturally, social media has become a platform for
people to share their experiences with approved drugs/biologics.
Spend some time looking into the role that social media might
play in serving as a platform for people to informally report on
potential adverse drug reactions. See the following to get you
started:
MedSafety Week: https://allaplusessays.com/order
“Using Facebook to Increase Spontaneous Reporting of Adverse
Drug Reactions” See Week 11 “Assignments” tab for link to PDF
Share your thoughts on how you think social media might be
used to help identify adverse drug reactions. What are the pros and
cons of this type of approach? How might we get the social media
ADRs transferred to databases like FAERS and VigiBase?
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The KLM airplane’s co-pilot reacts with ” we are currently at
take-off” to which the Air traffic Control tower reacts with
“alright”. In this manner, KLM expected leeway was endorsed and
started to move towards the runway landing area. Indeed the
pinnacle assumed, The KLM airplane was at take-off position and was
anticipating last freedom. The pinnacle pronounced another radio
call to KLM “hold on for take-off, I will call you” anyway this
message was not heard by KLM pilots because of glitch and
obstruction in radio signs. Hence, this report provides information
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