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THE PHARMA REVIEW
(SEPTEMBER – OCTOBER 2020) |
"Pharmacovigilance and its
Role in Combating Covid-19 Pandemic"
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Rutu M. Patel,
Khushi A. Pathak & Vimal Kumar |
Introduction: Corona viruses are a group of
viruses belonging to the family of Coronaviridae, which
infect both animals and humans. Human corona viruses can
cause mild disease similar to a common cold, while
others cause more severe disease (such as MERS - Middle
East Respiratory Syndrome and SARS – Severe Acute
Respiratory Syndrome). A new corona virus that
previously has not been identified in humans emerged in
Wuhan, China in December 2019. Whereas access to
treatment is a major priority in any emergency health
situation such as the COVID-19 pandemic, patient safety
must not be compromised by the need for access. Access
to the wrong, poor quality or unsafe product might have
worse consequences than lack of access. The global
pandemic have seen reports of increased sales and
perhaps hoarding of some medical products, such as
chloroquine, hydroxy chloroquine, and lopinavir/ritonavir,
in some countries, as well as increased sales of fake
medical products and medicines related to COVID-19, such
as hand sanitizers, and antiviral medications. The
COVID-19 pandemic has made patient safety headlines as
the world looks to existing therapies and new
innovations to treat those affected and help prevent
future infections. The current challenges posed by the
COVID-19 pandemic have also prompted regulatory agencies
to reconsider their requirements and have emphasized the
importance of electronic reporting to ensure data
exchange for patient safety.
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