Boston said he would fix Covid
- Thread starter Ucfmikes
- Start date
Well…., he’s not going to fix it with Horse 🐎 paste
COVID-19
Mary Van Beusekom | News Writer | CIDRAP News
|
Feb 18, 2022
Early treatment with the antiparasitic drug ivermectin does not lower the risk of severe disease when given to patients with mild to moderate COVID-19, according to a study today in JAMA Internal Medicine.
And a related study in the same journal finds connections between prescribing patterns for ivermectin and hydroxychloroquine by political-party vote share in 2020.
Average patient age was 62.5 years, 54.5% were women, 51.8% had received two doses of a COVID-19 vaccine, 75.3% had high blood pressure, 53.5% had diabetes, 37.6% had abnormal cholesterol levels, and 23.9% were obese.
Patients were randomly assigned in a 1:1 ratio to receive oral ivermectin daily for 5 days plus standard care (241 patients) or standard care only (249). Standard care consisted of treatment of symptoms and monitoring of clinical findings, laboratory test results, and chest imaging for signs of disease progression.
Severe disease was defined as hypoxia (low oxygen levels) requiring the use of supplemental oxygen to maintain oxygen saturation at 95% or higher.
Fifty-two of 241 patients in the ivermectin group (21.6%) and 43 of 249 patients in the standard-care-only group (17.3%) became severely ill (relative risk [RR], 1.25; 95% confidence interval [CI], 0.87 to 1.80).
There were no significant differences between the two groups in time to symptom resolution or rates of mechanical ventilation, intensive care unit (ICU) admission, 28-day in-hospital death, or adverse events. Four ivermectin recipients (1.7%) required mechanical ventilation, compared with 10 (4.0%) in the standard-care group (RR, 0.41; 95% CI, 0.13 to 1.30).
Six patients (2.4%) in the ivermectin group were admitted to an ICU, versus 8 (3.2%) in the control group (RR, 0.78; 95% CI, 0.27 to 2.20), and 3 ivermectin recipients (1.2%) and 10 controls (4.0%) died by 28 days (RR, 0.31; 95% CI, 0.09 to 1.11).
Forty-four patients (9.0%) had 55 adverse events, 33 of them in the ivermectin group. The most common adverse event was diarrhea, occurring in 14 (5.8%) in the ivermectin group and 4 (1.6%) in the standard-care group.
Five serious adverse events—four in the ivermectin group—were reported. Two patients had a heart attack, one had severe anemia, and one went into shock owing to fluid loss from severe diarrhea, while one in the control group had arterial bleeding in the abdomen. Adverse events led six patients to stop taking ivermectin and three to withdraw from the study. Thirteen patients (2.7%) died, most from COVID-19 pneumonia; no deaths were attributed to ivermectin.
"The notably higher incidence of AEs [adverse events] in the ivermectin group raises concerns about the use of this drug outside of trial settings and without medical supervision," the researchers wrote.
The authors noted that ivermectin may appear to be an attractive alternative to expensive antiviral medications in resource-limited regions such as Malaysia because it is inexpensive, easy to use, and broadly available.
However, the World Health Organization recommends against its use outside of clinical trials, and it is not US Food and Drug Administration (FDA)-approved for the prevention or treatment of COVID-19. Indeed, the Centers for Disease Control and Prevention (CDC) confirmed with the American Association of Poison Control Centers that reports of ivermectin-related adverse events increased in 2021 relative to before the pandemic.
"The study findings do not support the use of ivermectin for patients with COVID-19," the authors concluded.
Ivermectin futile for mild to moderate COVID-19, study finds
Filed Under:COVID-19
Mary Van Beusekom | News Writer | CIDRAP News
|
Feb 18, 2022
Early treatment with the antiparasitic drug ivermectin does not lower the risk of severe disease when given to patients with mild to moderate COVID-19, according to a study today in JAMA Internal Medicine.
And a related study in the same journal finds connections between prescribing patterns for ivermectin and hydroxychloroquine by political-party vote share in 2020.
Lack of efficacy, more adverse events
Doctors at 20 Malaysian government hospitals and a COVID-19 quarantine center conducted an open-label, randomized clinical trial on the use of ivermectin in the first week of COVID-19 symptom onset in hospitalized adults 50 years and older with mild or moderate illness and underlying medical conditions. The study took place from May 31 to Oct 25, 2021.Average patient age was 62.5 years, 54.5% were women, 51.8% had received two doses of a COVID-19 vaccine, 75.3% had high blood pressure, 53.5% had diabetes, 37.6% had abnormal cholesterol levels, and 23.9% were obese.
Patients were randomly assigned in a 1:1 ratio to receive oral ivermectin daily for 5 days plus standard care (241 patients) or standard care only (249). Standard care consisted of treatment of symptoms and monitoring of clinical findings, laboratory test results, and chest imaging for signs of disease progression.
Severe disease was defined as hypoxia (low oxygen levels) requiring the use of supplemental oxygen to maintain oxygen saturation at 95% or higher.
Fifty-two of 241 patients in the ivermectin group (21.6%) and 43 of 249 patients in the standard-care-only group (17.3%) became severely ill (relative risk [RR], 1.25; 95% confidence interval [CI], 0.87 to 1.80).
There were no significant differences between the two groups in time to symptom resolution or rates of mechanical ventilation, intensive care unit (ICU) admission, 28-day in-hospital death, or adverse events. Four ivermectin recipients (1.7%) required mechanical ventilation, compared with 10 (4.0%) in the standard-care group (RR, 0.41; 95% CI, 0.13 to 1.30).
Six patients (2.4%) in the ivermectin group were admitted to an ICU, versus 8 (3.2%) in the control group (RR, 0.78; 95% CI, 0.27 to 2.20), and 3 ivermectin recipients (1.2%) and 10 controls (4.0%) died by 28 days (RR, 0.31; 95% CI, 0.09 to 1.11).
Forty-four patients (9.0%) had 55 adverse events, 33 of them in the ivermectin group. The most common adverse event was diarrhea, occurring in 14 (5.8%) in the ivermectin group and 4 (1.6%) in the standard-care group.
Five serious adverse events—four in the ivermectin group—were reported. Two patients had a heart attack, one had severe anemia, and one went into shock owing to fluid loss from severe diarrhea, while one in the control group had arterial bleeding in the abdomen. Adverse events led six patients to stop taking ivermectin and three to withdraw from the study. Thirteen patients (2.7%) died, most from COVID-19 pneumonia; no deaths were attributed to ivermectin.
"The notably higher incidence of AEs [adverse events] in the ivermectin group raises concerns about the use of this drug outside of trial settings and without medical supervision," the researchers wrote.
The authors noted that ivermectin may appear to be an attractive alternative to expensive antiviral medications in resource-limited regions such as Malaysia because it is inexpensive, easy to use, and broadly available.
However, the World Health Organization recommends against its use outside of clinical trials, and it is not US Food and Drug Administration (FDA)-approved for the prevention or treatment of COVID-19. Indeed, the Centers for Disease Control and Prevention (CDC) confirmed with the American Association of Poison Control Centers that reports of ivermectin-related adverse events increased in 2021 relative to before the pandemic.
"The study findings do not support the use of ivermectin for patients with COVID-19," the authors concluded.
Fact that you call it horse paste shows how easy it is to fall for propaganda.
It’s so hilarious to watch IT specialist @Boston.Knight try to misinterpret a JAMA article to make his argument valid
Golden 😂😂😂
Golden 😂😂😂
Twitter brain brendabrowneye told him the JAMA article was WRONG!!!!!!!!! So, boston believed her like the good chud he is.
@Boston.Knight ?
COVID-19
Mary Van Beusekom | News Writer | CIDRAP News
|
Feb 18, 2022
Early treatment with the antiparasitic drug ivermectin does not lower the risk of severe disease when given to patients with mild to moderate COVID-19, according to a study today in JAMA Internal Medicine.
And a related study in the same journal finds connections between prescribing patterns for ivermectin and hydroxychloroquine by political-party vote share in 2020.
Average patient age was 62.5 years, 54.5% were women, 51.8% had received two doses of a COVID-19 vaccine, 75.3% had high blood pressure, 53.5% had diabetes, 37.6% had abnormal cholesterol levels, and 23.9% were obese.
Patients were randomly assigned in a 1:1 ratio to receive oral ivermectin daily for 5 days plus standard care (241 patients) or standard care only (249). Standard care consisted of treatment of symptoms and monitoring of clinical findings, laboratory test results, and chest imaging for signs of disease progression.
Severe disease was defined as hypoxia (low oxygen levels) requiring the use of supplemental oxygen to maintain oxygen saturation at 95% or higher.
Fifty-two of 241 patients in the ivermectin group (21.6%) and 43 of 249 patients in the standard-care-only group (17.3%) became severely ill (relative risk [RR], 1.25; 95% confidence interval [CI], 0.87 to 1.80).
There were no significant differences between the two groups in time to symptom resolution or rates of mechanical ventilation, intensive care unit (ICU) admission, 28-day in-hospital death, or adverse events. Four ivermectin recipients (1.7%) required mechanical ventilation, compared with 10 (4.0%) in the standard-care group (RR, 0.41; 95% CI, 0.13 to 1.30).
Six patients (2.4%) in the ivermectin group were admitted to an ICU, versus 8 (3.2%) in the control group (RR, 0.78; 95% CI, 0.27 to 2.20), and 3 ivermectin recipients (1.2%) and 10 controls (4.0%) died by 28 days (RR, 0.31; 95% CI, 0.09 to 1.11).
Forty-four patients (9.0%) had 55 adverse events, 33 of them in the ivermectin group. The most common adverse event was diarrhea, occurring in 14 (5.8%) in the ivermectin group and 4 (1.6%) in the standard-care group.
Five serious adverse events—four in the ivermectin group—were reported. Two patients had a heart attack, one had severe anemia, and one went into shock owing to fluid loss from severe diarrhea, while one in the control group had arterial bleeding in the abdomen. Adverse events led six patients to stop taking ivermectin and three to withdraw from the study. Thirteen patients (2.7%) died, most from COVID-19 pneumonia; no deaths were attributed to ivermectin.
"The notably higher incidence of AEs [adverse events] in the ivermectin group raises concerns about the use of this drug outside of trial settings and without medical supervision," the researchers wrote.
The authors noted that ivermectin may appear to be an attractive alternative to expensive antiviral medications in resource-limited regions such as Malaysia because it is inexpensive, easy to use, and broadly available.
However, the World Health Organization recommends against its use outside of clinical trials, and it is not US Food and Drug Administration (FDA)-approved for the prevention or treatment of COVID-19. Indeed, the Centers for Disease Control and Prevention (CDC) confirmed with the American Association of Poison Control Centers that reports of ivermectin-related adverse events increased in 2021 relative to before the pandemic.
"The study findings do not support the use of ivermectin for patients with COVID-19," the authors concluded.
Ivermectin futile for mild to moderate COVID-19, study finds
Filed Under:COVID-19
Mary Van Beusekom | News Writer | CIDRAP News
|
Feb 18, 2022
Early treatment with the antiparasitic drug ivermectin does not lower the risk of severe disease when given to patients with mild to moderate COVID-19, according to a study today in JAMA Internal Medicine.
And a related study in the same journal finds connections between prescribing patterns for ivermectin and hydroxychloroquine by political-party vote share in 2020.
Lack of efficacy, more adverse events
Doctors at 20 Malaysian government hospitals and a COVID-19 quarantine center conducted an open-label, randomized clinical trial on the use of ivermectin in the first week of COVID-19 symptom onset in hospitalized adults 50 years and older with mild or moderate illness and underlying medical conditions. The study took place from May 31 to Oct 25, 2021.Average patient age was 62.5 years, 54.5% were women, 51.8% had received two doses of a COVID-19 vaccine, 75.3% had high blood pressure, 53.5% had diabetes, 37.6% had abnormal cholesterol levels, and 23.9% were obese.
Patients were randomly assigned in a 1:1 ratio to receive oral ivermectin daily for 5 days plus standard care (241 patients) or standard care only (249). Standard care consisted of treatment of symptoms and monitoring of clinical findings, laboratory test results, and chest imaging for signs of disease progression.
Severe disease was defined as hypoxia (low oxygen levels) requiring the use of supplemental oxygen to maintain oxygen saturation at 95% or higher.
Fifty-two of 241 patients in the ivermectin group (21.6%) and 43 of 249 patients in the standard-care-only group (17.3%) became severely ill (relative risk [RR], 1.25; 95% confidence interval [CI], 0.87 to 1.80).
There were no significant differences between the two groups in time to symptom resolution or rates of mechanical ventilation, intensive care unit (ICU) admission, 28-day in-hospital death, or adverse events. Four ivermectin recipients (1.7%) required mechanical ventilation, compared with 10 (4.0%) in the standard-care group (RR, 0.41; 95% CI, 0.13 to 1.30).
Six patients (2.4%) in the ivermectin group were admitted to an ICU, versus 8 (3.2%) in the control group (RR, 0.78; 95% CI, 0.27 to 2.20), and 3 ivermectin recipients (1.2%) and 10 controls (4.0%) died by 28 days (RR, 0.31; 95% CI, 0.09 to 1.11).
Forty-four patients (9.0%) had 55 adverse events, 33 of them in the ivermectin group. The most common adverse event was diarrhea, occurring in 14 (5.8%) in the ivermectin group and 4 (1.6%) in the standard-care group.
Five serious adverse events—four in the ivermectin group—were reported. Two patients had a heart attack, one had severe anemia, and one went into shock owing to fluid loss from severe diarrhea, while one in the control group had arterial bleeding in the abdomen. Adverse events led six patients to stop taking ivermectin and three to withdraw from the study. Thirteen patients (2.7%) died, most from COVID-19 pneumonia; no deaths were attributed to ivermectin.
"The notably higher incidence of AEs [adverse events] in the ivermectin group raises concerns about the use of this drug outside of trial settings and without medical supervision," the researchers wrote.
The authors noted that ivermectin may appear to be an attractive alternative to expensive antiviral medications in resource-limited regions such as Malaysia because it is inexpensive, easy to use, and broadly available.
However, the World Health Organization recommends against its use outside of clinical trials, and it is not US Food and Drug Administration (FDA)-approved for the prevention or treatment of COVID-19. Indeed, the Centers for Disease Control and Prevention (CDC) confirmed with the American Association of Poison Control Centers that reports of ivermectin-related adverse events increased in 2021 relative to before the pandemic.
"The study findings do not support the use of ivermectin for patients with COVID-19," the authors concluded.
Ivermectin futile for mild to moderate COVID-19, study finds
Filed Under:COVID-19
Mary Van Beusekom | News Writer | CIDRAP News
|
Feb 18, 2022
Early treatment with the antiparasitic drug ivermectin does not lower the risk of severe disease when given to patients with mild to moderate COVID-19, according to a study today in JAMA Internal Medicine.
And a related study in the same journal finds connections between prescribing patterns for ivermectin and hydroxychloroquine by political-party vote share in 2020.
Lack of efficacy, more adverse events
Doctors at 20 Malaysian government hospitals and a COVID-19 quarantine center conducted an open-label, randomized clinical trial on the use of ivermectin in the first week of COVID-19 symptom onset in hospitalized adults 50 years and older with mild or moderate illness and underlying medical conditions. The study took place from May 31 to Oct 25, 2021.Average patient age was 62.5 years, 54.5% were women, 51.8% had received two doses of a COVID-19 vaccine, 75.3% had high blood pressure, 53.5% had diabetes, 37.6% had abnormal cholesterol levels, and 23.9% were obese.
Patients were randomly assigned in a 1:1 ratio to receive oral ivermectin daily for 5 days plus standard care (241 patients) or standard care only (249). Standard care consisted of treatment of symptoms and monitoring of clinical findings, laboratory test results, and chest imaging for signs of disease progression.
Severe disease was defined as hypoxia (low oxygen levels) requiring the use of supplemental oxygen to maintain oxygen saturation at 95% or higher.
Fifty-two of 241 patients in the ivermectin group (21.6%) and 43 of 249 patients in the standard-care-only group (17.3%) became severely ill (relative risk [RR], 1.25; 95% confidence interval [CI], 0.87 to 1.80).
There were no significant differences between the two groups in time to symptom resolution or rates of mechanical ventilation, intensive care unit (ICU) admission, 28-day in-hospital death, or adverse events. Four ivermectin recipients (1.7%) required mechanical ventilation, compared with 10 (4.0%) in the standard-care group (RR, 0.41; 95% CI, 0.13 to 1.30).
Six patients (2.4%) in the ivermectin group were admitted to an ICU, versus 8 (3.2%) in the control group (RR, 0.78; 95% CI, 0.27 to 2.20), and 3 ivermectin recipients (1.2%) and 10 controls (4.0%) died by 28 days (RR, 0.31; 95% CI, 0.09 to 1.11).
Forty-four patients (9.0%) had 55 adverse events, 33 of them in the ivermectin group. The most common adverse event was diarrhea, occurring in 14 (5.8%) in the ivermectin group and 4 (1.6%) in the standard-care group.
Five serious adverse events—four in the ivermectin group—were reported. Two patients had a heart attack, one had severe anemia, and one went into shock owing to fluid loss from severe diarrhea, while one in the control group had arterial bleeding in the abdomen. Adverse events led six patients to stop taking ivermectin and three to withdraw from the study. Thirteen patients (2.7%) died, most from COVID-19 pneumonia; no deaths were attributed to ivermectin.
"The notably higher incidence of AEs [adverse events] in the ivermectin group raises concerns about the use of this drug outside of trial settings and without medical supervision," the researchers wrote.
The authors noted that ivermectin may appear to be an attractive alternative to expensive antiviral medications in resource-limited regions such as Malaysia because it is inexpensive, easy to use, and broadly available.
However, the World Health Organization recommends against its use outside of clinical trials, and it is not US Food and Drug Administration (FDA)-approved for the prevention or treatment of COVID-19. Indeed, the Centers for Disease Control and Prevention (CDC) confirmed with the American Association of Poison Control Centers that reports of ivermectin-related adverse events increased in 2021 relative to before the pandemic.
"The study findings do not support the use of ivermectin for patients with COVID-19," the authors concluded.
COVID-19 V LYLE CRAWFORD (6 months of attrition)
Lyle Crawford, 42, San Antonio, TX, Fire Engineer, antivaxxer, dead from COVID.Lyle died on the 16th of February 2022 but he did not go out without a fight. It took six months for COVID to finally deliver the knockout blow. We shall start this story by verifying Lyle's right to be included...
www.sorryantivaxxer.com
Remember when Boston.Knight said the Tampa Bay Rays' catcher died from a vaccine?
ucf.forums.rivals.com
Remember when Boston.Knight said the Tampa Bay Rays' catcher died from a vaccine?
More died suddenly. I mean it's freaking everywhere now. All dying in their sleep. Sagat. In sleep. Included article on the Ray's bullpen catcher. https://www.wfla.com/community/health/coronavirus/13-year-old-dies-in-sleep-after-getting-covid-19-vaccine-cdc-investigating/...
ucf.forums.rivals.com
Remember when Boston.Knight said the Tampa Bay Rays' catcher died from a vaccine?
More died suddenly. I mean it's freaking everywhere now. All dying in their sleep. Sagat. In sleep. Included article on the Ray's bullpen catcher. https://www.wfla.com/community/health/coronavirus/13-year-old-dies-in-sleep-after-getting-covid-19-vaccine-cdc-investigating/...
ucf.forums.rivals.com
Remember when Boston.Knight said the Tampa Bay Rays' catcher died from a vaccine?
More died suddenly. I mean it's freaking everywhere now. All dying in their sleep. Sagat. In sleep. Included article on the Ray's bullpen catcher. https://www.wfla.com/community/health/coronavirus/13-year-old-dies-in-sleep-after-getting-covid-19-vaccine-cdc-investigating/...
ucf.forums.rivals.com
Remember when Boston.Knight said the Tampa Bay Rays' catcher died from a vaccine?
More died suddenly. I mean it's freaking everywhere now. All dying in their sleep. Sagat. In sleep. Included article on the Ray's bullpen catcher. https://www.wfla.com/community/health/coronavirus/13-year-old-dies-in-sleep-after-getting-covid-19-vaccine-cdc-investigating/...
ucf.forums.rivals.com
Remember when Boston.Knight said the Tampa Bay Rays' catcher died from a vaccine?
More died suddenly. I mean it's freaking everywhere now. All dying in their sleep. Sagat. In sleep. Included article on the Ray's bullpen catcher. https://www.wfla.com/community/health/coronavirus/13-year-old-dies-in-sleep-after-getting-covid-19-vaccine-cdc-investigating/...
ucf.forums.rivals.com
Remember when Boston.Knight said the Tampa Bay Rays' catcher died from a vaccine?
More died suddenly. I mean it's freaking everywhere now. All dying in their sleep. Sagat. In sleep. Included article on the Ray's bullpen catcher. https://www.wfla.com/community/health/coronavirus/13-year-old-dies-in-sleep-after-getting-covid-19-vaccine-cdc-investigating/...
ucf.forums.rivals.com
Remember when Boston.Knight said the Tampa Bay Rays' catcher died from a vaccine?
More died suddenly. I mean it's freaking everywhere now. All dying in their sleep. Sagat. In sleep. Included article on the Ray's bullpen catcher. https://www.wfla.com/community/health/coronavirus/13-year-old-dies-in-sleep-after-getting-covid-19-vaccine-cdc-investigating/...
ucf.forums.rivals.com
Remember when Boston.Knight said the Tampa Bay Rays' catcher died from a vaccine?
More died suddenly. I mean it's freaking everywhere now. All dying in their sleep. Sagat. In sleep. Included article on the Ray's bullpen catcher. https://www.wfla.com/community/health/coronavirus/13-year-old-dies-in-sleep-after-getting-covid-19-vaccine-cdc-investigating/...
ucf.forums.rivals.com
Remember when Boston.Knight said the Tampa Bay Rays' catcher died from a vaccine?
More died suddenly. I mean it's freaking everywhere now. All dying in their sleep. Sagat. In sleep. Included article on the Ray's bullpen catcher. https://www.wfla.com/community/health/coronavirus/13-year-old-dies-in-sleep-after-getting-covid-19-vaccine-cdc-investigating/...
ucf.forums.rivals.com
Remember when Boston.Knight said the Tampa Bay Rays' catcher died from a vaccine?
More died suddenly. I mean it's freaking everywhere now. All dying in their sleep. Sagat. In sleep. Included article on the Ray's bullpen catcher. https://www.wfla.com/community/health/coronavirus/13-year-old-dies-in-sleep-after-getting-covid-19-vaccine-cdc-investigating/...
ucf.forums.rivals.com
22) 67 or 11
23) Fool
At this rate it will be 30 -50 years to pass the parrot 🦜. 😂😂😂
Oh well. Another Freedumb fighter dying from COVID
www.sorryantivaxxer.com
Rachael D’Avanzo, 39, Sandy, OR, Mom of 5, Anti-vaxxer, Dead from Covid
We stumbled upon Rachael D’Avanzo by accident. We were working on a different anti-vaxxer story and it led us to Rachael. Rachael has five beautiful young children. She's only 39 years old and the epitome of health. She was promoting an online HITT fitness class at the beginning of the pandemic...
www.sorryantivaxxer.com
Ivermectin futile for mild to moderate COVID-19, study finds
Filed Under:COVID-19
Mary Van Beusekom | News Writer | CIDRAP News
|
Feb 18, 2022
Early treatment with the antiparasitic drug ivermectin does not lower the risk of severe disease when given to patients with mild to moderate COVID-19, according to a study today in JAMA Internal Medicine.
And a related study in the same journal finds connections between prescribing patterns for ivermectin and hydroxychloroquine by political-party vote share in 2020.
Lack of efficacy, more adverse events
Doctors at 20 Malaysian government hospitals and a COVID-19 quarantine center conducted an open-label, randomized clinical trial on the use of ivermectin in the first week of COVID-19 symptom onset in hospitalized adults 50 years and older with mild or moderate illness and underlying medical conditions. The study took place from May 31 to Oct 25, 2021.Average patient age was 62.5 years, 54.5% were women, 51.8% had received two doses of a COVID-19 vaccine, 75.3% had high blood pressure, 53.5% had diabetes, 37.6% had abnormal cholesterol levels, and 23.9% were obese.
Patients were randomly assigned in a 1:1 ratio to receive oral ivermectin daily for 5 days plus standard care (241 patients) or standard care only (249). Standard care consisted of treatment of symptoms and monitoring of clinical findings, laboratory test results, and chest imaging for signs of disease progression.
Severe disease was defined as hypoxia (low oxygen levels) requiring the use of supplemental oxygen to maintain oxygen saturation at 95% or higher.
Fifty-two of 241 patients in the ivermectin group (21.6%) and 43 of 249 patients in the standard-care-only group (17.3%) became severely ill (relative risk [RR], 1.25; 95% confidence interval [CI], 0.87 to 1.80).
There were no significant differences between the two groups in time to symptom resolution or rates of mechanical ventilation, intensive care unit (ICU) admission, 28-day in-hospital death, or adverse events. Four ivermectin recipients (1.7%) required mechanical ventilation, compared with 10 (4.0%) in the standard-care group (RR, 0.41; 95% CI, 0.13 to 1.30).
Six patients (2.4%) in the ivermectin group were admitted to an ICU, versus 8 (3.2%) in the control group (RR, 0.78; 95% CI, 0.27 to 2.20), and 3 ivermectin recipients (1.2%) and 10 controls (4.0%) died by 28 days (RR, 0.31; 95% CI, 0.09 to 1.11).
Forty-four patients (9.0%) had 55 adverse events, 33 of them in the ivermectin group. The most common adverse event was diarrhea, occurring in 14 (5.8%) in the ivermectin group and 4 (1.6%) in the standard-care group.
Five serious adverse events—four in the ivermectin group—were reported. Two patients had a heart attack, one had severe anemia, and one went into shock owing to fluid loss from severe diarrhea, while one in the control group had arterial bleeding in the abdomen. Adverse events led six patients to stop taking ivermectin and three to withdraw from the study. Thirteen patients (2.7%) died, most from COVID-19 pneumonia; no deaths were attributed to ivermectin.
"The notably higher incidence of AEs [adverse events] in the ivermectin group raises concerns about the use of this drug outside of trial settings and without medical supervision," the researchers wrote.
The authors noted that ivermectin may appear to be an attractive alternative to expensive antiviral medications in resource-limited regions such as Malaysia because it is inexpensive, easy to use, and broadly available.
However, the World Health Organization recommends against its use outside of clinical trials, and it is not US Food and Drug Administration (FDA)-approved for the prevention or treatment of COVID-19. Indeed, the Centers for Disease Control and Prevention (CDC) confirmed with the American Association of Poison Control Centers that reports of ivermectin-related adverse events increased in 2021 relative to before the pandemic.
"The study findings do not support the use of ivermectin for patients with COVID-19," the authors concluded.
Jesse Boshears, 20, Perryville, AR, Arkansas Tech Football Player, Unvaxxed, Dead From COVID
(Update 3/4/22): After 8 months, Jesse Shane Boshears passed away. See below. We saw the news of Vaxman having COVID and thought we'd jump in to help out. Since the start of the pandemic, the CDC reports that 5,681 people ages 18-29 years have passed away due to COVID. At Herman Cain Awards we...
www.sorryantivaxxer.com
Ivermectin futile for mild to moderate COVID-19, study finds
Filed Under:COVID-19
Mary Van Beusekom | News Writer | CIDRAP News
|
Feb 18, 2022
Early treatment with the antiparasitic drug ivermectin does not lower the risk of severe disease when given to patients with mild to moderate COVID-19, according to a study today in JAMA Internal Medicine.
And a related study in the same journal finds connections between prescribing patterns for ivermectin and hydroxychloroquine by political-party vote share in 2020.
Lack of efficacy, more adverse events
Doctors at 20 Malaysian government hospitals and a COVID-19 quarantine center conducted an open-label, randomized clinical trial on the use of ivermectin in the first week of COVID-19 symptom onset in hospitalized adults 50 years and older with mild or moderate illness and underlying medical conditions. The study took place from May 31 to Oct 25, 2021.Average patient age was 62.5 years, 54.5% were women, 51.8% had received two doses of a COVID-19 vaccine, 75.3% had high blood pressure, 53.5% had diabetes, 37.6% had abnormal cholesterol levels, and 23.9% were obese.
Patients were randomly assigned in a 1:1 ratio to receive oral ivermectin daily for 5 days plus standard care (241 patients) or standard care only (249). Standard care consisted of treatment of symptoms and monitoring of clinical findings, laboratory test results, and chest imaging for signs of disease progression.
Severe disease was defined as hypoxia (low oxygen levels) requiring the use of supplemental oxygen to maintain oxygen saturation at 95% or higher.
Fifty-two of 241 patients in the ivermectin group (21.6%) and 43 of 249 patients in the standard-care-only group (17.3%) became severely ill (relative risk [RR], 1.25; 95% confidence interval [CI], 0.87 to 1.80).
There were no significant differences between the two groups in time to symptom resolution or rates of mechanical ventilation, intensive care unit (ICU) admission, 28-day in-hospital death, or adverse events. Four ivermectin recipients (1.7%) required mechanical ventilation, compared with 10 (4.0%) in the standard-care group (RR, 0.41; 95% CI, 0.13 to 1.30).
Six patients (2.4%) in the ivermectin group were admitted to an ICU, versus 8 (3.2%) in the control group (RR, 0.78; 95% CI, 0.27 to 2.20), and 3 ivermectin recipients (1.2%) and 10 controls (4.0%) died by 28 days (RR, 0.31; 95% CI, 0.09 to 1.11).
Forty-four patients (9.0%) had 55 adverse events, 33 of them in the ivermectin group. The most common adverse event was diarrhea, occurring in 14 (5.8%) in the ivermectin group and 4 (1.6%) in the standard-care group.
Five serious adverse events—four in the ivermectin group—were reported. Two patients had a heart attack, one had severe anemia, and one went into shock owing to fluid loss from severe diarrhea, while one in the control group had arterial bleeding in the abdomen. Adverse events led six patients to stop taking ivermectin and three to withdraw from the study. Thirteen patients (2.7%) died, most from COVID-19 pneumonia; no deaths were attributed to ivermectin.
"The notably higher incidence of AEs [adverse events] in the ivermectin group raises concerns about the use of this drug outside of trial settings and without medical supervision," the researchers wrote.
The authors noted that ivermectin may appear to be an attractive alternative to expensive antiviral medications in resource-limited regions such as Malaysia because it is inexpensive, easy to use, and broadly available.
However, the World Health Organization recommends against its use outside of clinical trials, and it is not US Food and Drug Administration (FDA)-approved for the prevention or treatment of COVID-19. Indeed, the Centers for Disease Control and Prevention (CDC) confirmed with the American Association of Poison Control Centers that reports of ivermectin-related adverse events increased in 2021 relative to before the pandemic.
"The study findings do not support the use of ivermectin for patients with COVID-19," the authors concluded.
Brandon Moore, 31, Prairie Grove, Arkansas, Anti-vaxxer, Dead From Covid
Here we go again, another anti-vaxxer who effed around but her partner is doing the finding out. Let me introduce you to Courtney Jean Moore and her husband Brandon Moore. Brandon is the one finding out. He had no public anti-vaxx posts, but Courtney made up for his lack. Brandon was only 31...
www.sorryantivaxxer.com
Douglas J Hall, 31, Callaway, VA, Anti-vaxxer, Dead from Covid
Douglas James Hall, or DJ to his friends, was a driver for Nexhaul Trailer Company. He was married with a son and stepdaughter. On paper, he comes across as a typical, boring person, just your average anti-vaxxer. But we at the HCAz think he deserves a feature, as he had two things going for...
www.sorryantivaxxer.com
Brandon Fidler, 36, Wayland, MI, Truck Driver, anti-vaxxer, dead from COVID
According to social media posts (below), Brandon died on February 11, 2022 from COVID. Brandon is yet another anti-vaxx truck driver. Oh, and no matter how ignorant Brandon seems about vaccines, his wife is a nurse so there should be no excuse...except that she's also a paranormal investigator...
www.sorryantivaxxer.com
^^^^^^^^
I have a degree from UCF so what does that say? I could retire at 45. Multiple technical certificates and licenses. Must be lucky. 😉
I wouldn't say either way if I got vaccinated for the record. I've already said it is looking more and more like it is safe. Need a lab created vaccine for a lab created virus.
Remember when Boston.Knight said the Tampa Bay Rays' catcher died from a vaccine?
More died suddenly. I mean it's freaking everywhere now. All dying in their sleep. Sagat. In sleep. Included article on the Ray's bullpen catcher. https://www.wfla.com/community/health/coronavirus/13-year-old-dies-in-sleep-after-getting-covid-19-vaccine-cdc-investigating/...
ucf.forums.rivals.com
Safety of COVID-19 Vaccines
Updated Feb. 22, 2022
Languages
More than 539 million doses of COVID-19 vaccine had been given in the United States from December 14, 2020, through January 31, 2022. To view the current total number of COVID-19 vaccinations that have been administered in the United States, please visit the CDC COVID Data Tracker.
COVID-19 vaccines are safe and effective. COVID-19 vaccines were evaluated in tens of thousands of participants in clinical trials. The vaccines met the Food and Drug Administration’s (FDA’s) rigorous scientific standards for safety, effectiveness, and manufacturing quality needed to support emergency use authorization (EUA). Learn more about EUAs in this video.external icon
The Pfizer-BioNTech, Moderna, and Johnson & Johnson/Janssen COVID-19 vaccines will continue to undergo the most intensive safety monitoring in US history. This monitoring includes using both established and new safety monitoring systems to make sure that COVID-19 vaccines are safe.
Updated Feb. 22, 2022
Languages
What You Need to Know
- COVID-19 vaccines are safe and effective.
- Millions of people in the United States have received COVID-19 vaccines under the most intense safety monitoring in US history.
- CDC recommends you get a COVID-19 vaccine as soon as possible.
- If you are fully vaccinated, you can resume many activities that you did prior to the pandemic. Learn more about what you can do when you have been fully vaccinated.
Hundreds of Millions of People Have Safely Received a COVID-19 Vaccine
More than 539 million doses of COVID-19 vaccine had been given in the United States from December 14, 2020, through January 31, 2022. To view the current total number of COVID-19 vaccinations that have been administered in the United States, please visit the CDC COVID Data Tracker.
COVID-19 vaccines are safe and effective. COVID-19 vaccines were evaluated in tens of thousands of participants in clinical trials. The vaccines met the Food and Drug Administration’s (FDA’s) rigorous scientific standards for safety, effectiveness, and manufacturing quality needed to support emergency use authorization (EUA). Learn more about EUAs in this video.external icon
The Pfizer-BioNTech, Moderna, and Johnson & Johnson/Janssen COVID-19 vaccines will continue to undergo the most intensive safety monitoring in US history. This monitoring includes using both established and new safety monitoring systems to make sure that COVID-19 vaccines are safe.
Common Side Effects
After COVID-19 vaccination, some people may feel ill, with symptoms like fever or tiredness for a day or two after receiving the vaccine. These symptoms are normal and are signs that the body is building immunity. Some people have no side effects. Others have reported common side effects after COVID-19 vaccination,such as:- Swelling, redness, and pain at the injection site
- Fever
- Headache
- Tiredness
- Muscle pain
- Chills
- Nausea
Serious Safety Problems Are Rare
In rare cases, people have experienced serious health events after COVID-19 vaccination. Any health problem that happens after vaccination is considered an adverse event. An adverse event can be caused by the vaccine or can be caused by a coincidental event not related to the vaccine.
Safety of COVID-19 Vaccines
Updated Feb. 22, 2022
Languages
More than 539 million doses of COVID-19 vaccine had been given in the United States from December 14, 2020, through January 31, 2022. To view the current total number of COVID-19 vaccinations that have been administered in the United States, please visit the CDC COVID Data Tracker.
COVID-19 vaccines are safe and effective. COVID-19 vaccines were evaluated in tens of thousands of participants in clinical trials. The vaccines met the Food and Drug Administration’s (FDA’s) rigorous scientific standards for safety, effectiveness, and manufacturing quality needed to support emergency use authorization (EUA). Learn more about EUAs in this video.external icon
The Pfizer-BioNTech, Moderna, and Johnson & Johnson/Janssen COVID-19 vaccines will continue to undergo the most intensive safety monitoring in US history. This monitoring includes using both established and new safety monitoring systems to make sure that COVID-19 vaccines are safe.
Updated Feb. 22, 2022
Languages
What You Need to Know
- COVID-19 vaccines are safe and effective.
- Millions of people in the United States have received COVID-19 vaccines under the most intense safety monitoring in US history.
- CDC recommends you get a COVID-19 vaccine as soon as possible.
- If you are fully vaccinated, you can resume many activities that you did prior to the pandemic. Learn more about what you can do when you have been fully vaccinated.
Hundreds of Millions of People Have Safely Received a COVID-19 Vaccine
More than 539 million doses of COVID-19 vaccine had been given in the United States from December 14, 2020, through January 31, 2022. To view the current total number of COVID-19 vaccinations that have been administered in the United States, please visit the CDC COVID Data Tracker.
COVID-19 vaccines are safe and effective. COVID-19 vaccines were evaluated in tens of thousands of participants in clinical trials. The vaccines met the Food and Drug Administration’s (FDA’s) rigorous scientific standards for safety, effectiveness, and manufacturing quality needed to support emergency use authorization (EUA). Learn more about EUAs in this video.external icon
The Pfizer-BioNTech, Moderna, and Johnson & Johnson/Janssen COVID-19 vaccines will continue to undergo the most intensive safety monitoring in US history. This monitoring includes using both established and new safety monitoring systems to make sure that COVID-19 vaccines are safe.
Common Side Effects
After COVID-19 vaccination, some people may feel ill, with symptoms like fever or tiredness for a day or two after receiving the vaccine. These symptoms are normal and are signs that the body is building immunity. Some people have no side effects. Others have reported common side effects after COVID-19 vaccination,such as:- Swelling, redness, and pain at the injection site
- Fever
- Headache
- Tiredness
- Muscle pain
- Chills
- Nausea
Serious Safety Problems Are Rare
In rare cases, people have experienced serious health events after COVID-19 vaccination. Any health problem that happens after vaccination is considered an adverse event. An adverse event can be caused by the vaccine or can be caused by a coincidental event not related to the vaccine.
sorryantivaxxer.com | stories of anti-vaxxers who died from COVID.
They thought COVID was a scam, until they lay dying from it. sorryantivaxxer.com tells their story using their own facebook and twitter posts.
www.sorryantivaxxer.com
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OT: War in Israel, anti Israeli protests across college campuses- Latest: HoopingKnight51
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