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.
PLoS ONE,
Journal Year:
2023,
Volume and Issue:
18(7), P. e0288350 - e0288350
Published: July 14, 2023
Coronavirus
disease
of
2019
(COVID-19)
is
a
global
health
problem.
The
impact
chronic
liver
diseases
on
the
course
and
outcome
COVID-19
still
subject
research.
aim
this
study
was
to
show
characteristics
patients
with
diseases,
establish
risk
factors
for
unfavourable
outcome.
Expert Review of Clinical Pharmacology,
Journal Year:
2022,
Volume and Issue:
15(6), P. 759 - 766
Published: May 17, 2022
This
meta-analysis
of
randomized
controlled
trials
(RCTs)
investigated
the
clinical
efficacy
and
safety
favipiravir
for
patients
with
mild-to-critical
COVID-19.PubMed,
Web
Science,
Ovid
Medline,
Embase,
Cochrane
Central
Register
Controlled
Trials
were
searched
RCTs
published
before
30
October
2021.
Only
that
compared
-based
antiviral
regimens
(study
group)
other
alternative
treatments
or
placebos
(control
in
COVID-19
included.Overall,
improvement
rate
was
significantly
higher
study
group
than
control
at
assessment
conducted
after
14
days
(OR,
1.83;
95%
CI,
1.12-2.98).
The
virological
eradication
28
2.09;
1.15-3.78).
No
significant
difference
observed
rates
invasive
mechanical
ventilation
requirement
ICU
admission,
mortality,
risk
an
adverse
event
between
groups.Except
within
days,
favipiravir-based
treatment
did
not
provide
additional
benefit
COVID-19.
Therefore,
more
evidence
is
necessary.
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.