Deleted Journal,
Journal Year:
2024,
Volume and Issue:
1(1)
Published: Oct. 14, 2024
Abstract
Background
The
Coronavirus
Disease
of
2019
(COVID-19)
pandemic
motivated
research
efforts
to
address
this
catastrophe
from
the
beginning
2020
present.
year
2021
is
coming
an
end,
and
several
developments
in
pharmacotherapy
for
COVID-19
have
occurred.
In
terms
antiviral
therapy,
monoclonal
antibody
combinations
become
one
type
immunotherapy.
Remdesivir
favipiravir
are
two
medications
typically
used
treat
COVID-19.
Paxlovid
(nirmatrelvir
plus
ritonavir)
molnupiravir
other
agents
purpose
study
was
compare
effects
antibodies
(casirivimab
imdevimab),
remdesivir,
on
swab
results
hospitalized
patients
with
at
discharge.
Methods
This
a
phase
IV
non-randomized
controlled
trial
(<
300
as
sample
size)
no
comparison
placebo.
study,
265
confirmed
by
polymerase
chain
reaction
(PCR)
indications
medication
were
into
three
groups
ratio
(1:2:2):
REGN3048-3051
(group
A),
remdesivir
B),
C).
A
nonrandomized
single-blind
design
used.
study's
provided
Hospital
Mansoura
University.
Following
ethical
approval,
conducted
approximately
6
months.
Results
Compared
favipiravir,
casirivimab
imdevimab
cause
less
hepatotoxicity,
renal
impairment,
more
negative
tested
antivirals
also
had
significant
adverse
effects.
All
considered
safe
based
these
findings.
Conclusion
result
better
clinical
outcomes.
toxicity.
Trial
registration
:
Clinicaltrials.gov,
NCT05502081,
16/08/2022.
Clinical Microbiology and Infection,
Journal Year:
2022,
Volume and Issue:
28(4), P. 602 - 608
Published: Jan. 11, 2022
To
evaluate
whether
favipiravir
reduces
the
time
to
viral
clearance
as
documented
by
negative
RT-PCR
results
for
severe
acute
respiratory
syndrome
coronavirus
2
in
mild
cases
of
disease
2019
(COVID-19)
compared
placebo.
International Journal of General Medicine,
Journal Year:
2021,
Volume and Issue:
Volume 14, P. 8557 - 8571
Published: Nov. 1, 2021
Background:
The
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
is
a
novel
strain
that
causes
illnesses
known
as
disease
2019
(COVID-19).
Currently,
there
limited
information
regarding
the
therapeutic
management
for
this
disease.
Several
studies
have
stated
antivirals
drugs
such
remdesivir,
favipiravir,
and
lopinavir/ritonavir
may
potentially
inhibit
virus
from
spreading
to
host.
Objective:
aim
of
systematic
review
was
summarize
clinical
effectiveness
safety
on
COVID-19.
Methods:
PubMed
Cochrane
Library
databases
were
searched
up
July
2021
identify
eligible
experimental
randomized
controlled
trials
COVID-19
patients.
This
followed
Preferred
Reporting
Items
Systematic
Reviews
Meta-Analyses
(PRISMA)
guideline.
Results:
From
158
references,
15
included
in
review.
results
showed
remdesivir
has
some
potential
benefits
hospitalized
patients,
seen
improvements
faster
recovery
time,
less
duration
hospitalization,
fewer
side
effects
among
However,
impact
reducing
mortality
remains
uncertain.
Treatment
with
favipiravir
shown
promising
improvement
status
although
suggested
no
significant
differences
parameters
length
hospitalizations
recovery.
A
combination
other
supportive
therapy
more
favorable
outcomes
Furthermore,
use
patients
reported
compared
standard
care
notable
adverse
effect
reactions.
Conclusion:
study
provides
an
overview
evidence-based
role
thorough
assessment
benefit-risk
profile
urgently
needed.
current
based
very
available
data;
therefore,
further
well-designed
are
required.
Keywords:
COVID-19,
antiviral
drugs,
SARS-CoV-2,
lopinavir/ritonavir,
BMC Infectious Diseases,
Journal Year:
2022,
Volume and Issue:
22(1)
Published: Dec. 12, 2022
We
aimed
to
elucidate
differences
in
the
characteristics
of
patients
with
coronavirus
disease
2019
(COVID-19)
requiring
hospitalization
Japan,
by
COVID-19
waves,
from
conventional
strains
Delta
variant.We
used
secondary
data
a
database
and
performed
retrospective
cohort
study
that
included
3261
aged
≥
18
years
enrolled
78
hospitals
participated
Japan
Task
Force
between
February
2020
September
2021.Patients
hospitalized
during
second
(mean
age,
53.2
[standard
deviation
{SD},
±
18.9])
fifth
50.7
[SD
13.9])
waves
had
lower
mean
age
than
those
other
waves.
Patients
first
wave
longer
hospital
stay
(mean,
30.3
days
21.5],
p
<
0.0001),
post-hospitalization
complications,
such
as
bacterial
infections
(21.3%,
were
also
noticeable.
In
addition,
there
was
an
increase
use
drugs
remdesivir/baricitinib/tocilizumab/steroids
latter
wave,
exhibited
greater
number
presenting
symptoms,
higher
percentage
required
oxygen
therapy
at
time
admission.
However,
invasive
mechanical
ventilation
highest
mortality
rate
third
wave.We
identified
clinical
each
up
Japan.
The
associated
severity
on
admission,
rate,
ventilation.
Emerging Microbes & Infections,
Journal Year:
2022,
Volume and Issue:
11(1), P. 2197 - 2206
Published: Aug. 23, 2022
We
investigated
Favipiravir
(FPV)
efficacy
in
mild
cases
of
COVID-19
without
pneumonia
and
its
effects
towards
viral
clearance,
clinical
condition,
risk
development.
PCR-confirmed
SARS-CoV-2-infected
patients
were
enrolled
(2:1)
within
10
days
symptomatic
onset
into
FPV
control
arms.
The
former
received
1800
mg
twice-daily
(BID)
on
Day
1
800
BID
5-14
thereafter
until
negative
detection,
while
the
latter
only
supportive
care.
primary
endpoint
was
time
to
improvement,
defined
by
a
National
Early
Warning
Score
(NEWS)
≤1.
62
(41
female)
comprised
arm
(median
age:
32
years,
median
BMI:
22
kg/m²)
31
(19
28
kg/m²).
sustained
NEWS,
2
14
for
arms,
respectively
(adjusted
hazard
ratio
(aHR)
2.77,
95%
CI
1.57-4.88,
P
<
.001).
also
had
significantly
higher
likelihoods
improvement
after
enrolment
NEWS
(79%
vs.
32%
respectively,
8
(12.9%)
7
(22.6%)
arms
developed
at
(range)
6.5
(1-13)
treatment,
(P
=
.316).
All
recovered
well
complications.
can
conclude
that
early
treatment
associated
with
faster
improvement.Trial
registration:
Thai
Clinical
Trials
Registry
identifier:
TCTR20200514001.
Molecules,
Journal Year:
2022,
Volume and Issue:
27(23), P. 8562 - 8562
Published: Dec. 5, 2022
The
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
was
the
seventh
known
human
coronavirus,
and
it
identified
in
Wuhan,
Hubei
province,
China,
2020.
It
caused
highly
contagious
disease
called
2019
(COVID-19),
declared
a
global
pandemic
by
World
Health
Organization
(WHO)
on
11
March
A
great
number
of
studies
search
new
therapies
vaccines
have
been
carried
out
these
three
long
years,
producing
series
successes;
however,
need
for
more
effective
vaccines,
other
solutions
is
still
being
pursued.
This
review
represents
tracking
shot
current
pharmacological
used
treatment
COVID-19.
Clinical Pathology,
Journal Year:
2024,
Volume and Issue:
17
Published: Jan. 1, 2024
The
COVID-19
pandemic-led
worldwide
healthcare
crisis
necessitates
prompt
societal,
ecological,
and
medical
efforts
to
stop
or
reduce
the
rising
number
of
fatalities.
Numerous
mRNA
based
vaccines
for
viral
vectors
have
been
licensed
use
in
emergencies
which
showed
90%
95%
efficacy
preventing
SARS-CoV-2
infection.
However,
safety
issues,
vaccine
reluctance,
skepticism
remain
major
concerns
making
mass
vaccination
a
successful
approach
treat
COVID-19.
Hence,
alternative
therapeutics
is
needed
eradicating
global
burden
from
developed
low-resource
countries.
Repurposing
current
medications
drug
candidates
could
be
more
viable
option
treating
as
these
therapies
previously
passed
significant
checkpoints
development
patient
care.
Besides
vaccines,
this
review
focused
on
potential
usage
therapeutic
agents
including
antiviral,
antiparasitic,
antibacterial
drugs,
protease
inhibitors,
neuraminidase
monoclonal
antibodies
that
are
currently
undergoing
preclinical
clinical
investigations
assess
their
effectiveness
treatment
Among
repurposed
remdesivir
considered
most
promising
agent,
while
favipiravir,
molnupiravir,
paxlovid,
lopinavir/ritonavir
exhibited
improved
effects
terms
elimination
viruses.
outcomes
with
oseltamivir,
umifenovir,
disulfiram,
teicoplanin,
ivermectin
were
not
significant.
It
noteworthy
combining
multiple
drugs
therapy
showcases
impressive
managing
individuals
Tocilizumab
presently
employed
patients
who
exhibit
COVID-19-related
pneumonia.
antiviral
such
galidesivir,
griffithsin,
thapsigargin
under
trials
severe
symptoms.
Supportive
may
involve
corticosteroids,
convalescent
plasma,
stem
cells,
pooled
antibodies,
vitamins,
natural
substances.
This
study
provides
an
updated
progress
crucial
guide
inventing
novel
interventions
against
The Australian Journal of Anthropology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 4, 2025
Abstract
Drawing
on
14
months
of
ethnographic
research
in
Bangladesh,
I
analyse
how
the
COVID‐19
pandemic
intersected
with
global
and
local
healthcare
markets
2020
to
shape
public
health
governance
affecting
interests,
needs,
lives.
In
early
phase,
misuse
administrative
power
corruption
among
bureaucrats,
government
representatives,
political
leaders
became
apparent
Bangladesh.
It
fostered
private
catastrophes,
exposing
some
fraudulence
medical
equipment
provision
treatment
disease.
Due
state's
denial,
citizens
were
deprived
low‐cost
solutions
(e.g.
rapid
antigen
test
kits)
for
infection
detection.
Engaging
concept
disaster
capitalism,
argue
that
elusive
role
state,
politicised
ground
governance,
medicine
market
combined
sectors
ultimately
benefited
corporations
rather
than
urgent
needs
Bangladeshis.
Journal of Chemical Information and Modeling,
Journal Year:
2022,
Volume and Issue:
62(17), P. 4261 - 4269
Published: Aug. 19, 2022
Viral
infection
relies
on
the
hijacking
of
cellular
machineries
to
enforce
reproduction
infecting
virus
and
its
subsequent
diffusion.
In
this
context,
replication
viral
genome
is
a
key
step
performed
by
specific
enzymes,
i.e.,
polymerases.
The
SARS-CoV-2,
causative
agent
COVID-19
pandemics,
based
duplication
RNA
genome,
an
action
RNA-dependent
polymerase.
contribution,
using
highly
demanding
DFT/MM-MD
computations
coupled
2D-umbrella
sampling
techniques,
we
have
determined
chemical
mechanisms
leading
inclusion
nucleotide
in
nascent
strand.
These
results
highlight
high
efficiency
polymerase,
which
lowers
activation
free
energy
less
than
10
kcal/mol.
Furthermore,
SARS-CoV-2
polymerase
active
site
slightly
different
from
those
usually
found
other
similar
particular,
it
lacks
possibility
proton
shuttle
via
nearby
histidine.
Our
simulations
show
that
absence
partially
compensated
lysine
whose
assists
reaction,
opening
up
alternative,
but
efficient,
reactive
channel.
present
first
mechanistic
resolution
at
level
shed
light
unusual
enzymatic
reactivity
paving
way
for
future
rational
design
antivirals
targeting
emerging
viruses.