Peer-reviewed study in the American Journal of Therapeutics has identified
a very effective drug for use against the Wuhan Red Death (aka COVID-19).
The drug not only will help to prevent infection, it can be used to treat
an infection, and also is extremely effective for those patients with
post-COVID-19 syndrome (lingering and sometimes debilitating condition
after infection).

https://journals.lww.com/americantherapeutics/fulltext/2021/00000/review_of_the_emerging_evidence_demonstrating_the.4.aspx?fbclid=IwAR2lQQmnlvALejyMjPHoWQiRJxY9AoHCPljTO9uh8CTh4QkK_odmDmTXSZI

Selected highlights from this study are shared below.
Conclusions:

Meta-analyses based on 18 randomized controlled treatment trials of
ivermectin in COVID-19 have found large, statistically significant
reductions in mortality, time to clinical recovery, and time to viral
clearance. Furthermore, results from numerous controlled prophylaxis trials
report significantly reduced risks of contracting COVID-19 with the regular
use of ivermectin. Finally, the many examples of ivermectin distribution
campaigns leading to rapid population-wide decreases in morbidity and
mortality indicate that an oral agent effective in all phases of COVID-19
has been identified.

Exposure prophylaxis studies of ivermectin's ability to prevent
transmission of COVID-19

Data are also now available showing large and statistically significant
decreases in the transmission of COVID-19 among human subjects based on
data from 3 randomized controlled trials (RCTs) and 5 observational
controlled trials (OCTs) with 4 of the 8 (2 of them RCTs) published in
peer-reviewed journals.40–
Clinical studies on the efficacy of ivermectin in treating mildly ill
outpatients

Currently, 7 trials that include a total of more than 3000 patients with
mild outpatient illness have been completed, a set composed of 7 RCTs and 4
case series.49–60

The largest, a double-blinded RCT by Mahmud49 was conducted in Dhaka,
Bangladesh, and targeted 400 patients with 363 patients completing the
study. In this study, as in many other of the clinical studies to be
reviewed, either a tetracycline (doxycycline) or macrolide antibiotic
(azithromycin) was included as part of the treatment. The importance of
including antibiotics such as doxycycline or azithromycin is unclear;
however, both tetracycline and macrolide antibiotics have recognized
anti-inflammatory, immunomodulatory, and even antiviral effects (58–61).
Although the posted data from this study does not specify the amount of
mildly ill outpatients versus hospitalized patients treated, important
clinical outcomes were profoundly affected, with increased rates of early
improvement (60.7% vs. 44.4% *P* < 0.03) and decreased rates of clinical
deterioration (8.7% vs. 17.8%, *P* < 0.02). Given that mildly ill
outpatients mainly comprised the study cohort, only 2 deaths were observed
(both in the control group).
Clinical studies of the efficacy of ivermectin in hospitalized patients

Studies of ivermectin among more severely ill hospitalized patients include
6 RCTs, 5 OCTs, and a database analysis study.45,51–53,63–70

The largest RCT in hospitalized patients was performed concurrent with the
prophylaxis study reviewed above by Elgazzar et al.45 Four hundred patients
were randomized among 4 treatment groups of 100 patients each. Groups 1 and
2 included mild/moderate illness patients alone, with group 1 treated with
one dose 0.4 mg/kg ivermectin plus standard of care (SOC) and group 2
received hydroxychloroquine 400 mg twice on day 1 then 200 mg twice daily
for 5 days plus standard of care. There was a statistically significant
lower rate of progression in the ivermectin-treated group (1% vs. 22%, *P*
< 0.001), with no deaths and 4 deaths, respectively. Groups 3 and 4
included only severely ill patients, with group 3 again treated with a
single dose of 0.4 mg/kg plus SOC, whereas group 4 received
hydroxychloroquine plus SOC. In this severely ill subgroup, the differences
in outcomes were even larger, with lower rates of progression 4% versus 30%
and mortality 2% versus 20% (*P* < 0.001).
Ivermectin in post-COVID-19 syndrome

Increasing reports of persistent, vexing, and even disabling symptoms after
recovery from acute COVID-19 have been reported and that many have termed
the condition as “Long COVID” and patients as “long haulers,” estimated to
occur in approximately 10%–30% of cases.71–73 Generally considered as a
postviral syndrome consisting of a chronic and sometimes disabling
constellation of symptoms which include, in order, fatigue, shortness of
breath, joint pains, and chest pain. Many patients describe their most
disabling symptom as impaired memory and concentration, often with extreme
fatigue, described as “brain fog,” and is highly suggestive of the
condition myalgic encephalomyelitis/chronic fatigue syndrome, a condition
well reported to begin after viral infections, in particular with
Epstein–Barr virus. Although no specific treatments have been identified
for Long COVID, a recent manuscript by Aguirre-Chang et al from the
National University of San Marcos in Peru reported on their experience with
ivermectin in such patients.74 They treated 33 patients who were between 4
and 12 weeks from the onset of symptoms with escalating doses of
ivermectin; 0.2 mg/kg for 2 days if mild and 0.4 mg/kg for 2 days if
moderate, with doses extended if symptoms persisted. They found that in
87.9% of the patients, resolution of all symptoms was observed after 2
doses with an additional 7% reporting complete resolution after additional
doses. Their experience suggests the need for controlled studies to better
test efficacy in this vexing syndrome.
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Max
Charleston SC
_______________________________________
http://www.okiebenz.com

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