Nm

[Crazyhole]

Bruh. Just get the jab and go fight some Nazis.

 

[Ucfmikes]

View embedded media

Bruh. Just get the jab and go fight some Nazis.

I'm sure he already had covid and has antibodies from the sniffles. Get woke!

 

[Ucfmikes]

Safety of COVID-19 Vaccines
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.

 

[Ucfmikes]

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.

 

[Crazyhole]

Anybody care to posit a theory on why this is happening?

 

[hemightbejeremy]

View embedded media

Anybody care to posit a theory on why this is happening?

Covid

 

[Ucfmikes]

View embedded media

Anybody care to posit a theory on why this is happening?

Safety of COVID-19 Vaccines
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.

 

[Ucfmikes]

View embedded media

Anybody care to posit a theory on why this is happening?

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.

 

[Ucfmikes]

Anybody care

 

[hemightbejeremy]

View embedded media

Anybody care to posit a theory on why this is happening?

Again, this requires a basic understanding of middle school level math. During Covid, the death rate for the 85+ population went from 14.3% to 15.5% chance per year (an 8% increase). For the 35-44 population the death rate went from 0.25% to 0.38% chance per year (a 50+% increase). In reality the odds of an elderly dying increased by 1.2% during Covid and for a 35-44 year old increased by 1/10 of that amount. It’s basic to anyone who isn’t as dense as a black hole. Now this concludes your math lesson for the day.

 

[Boston.Knight]

Peter McCullough rips US safety and quality a new one. Everything he is saying is spot on. Made in America is DOA thanks to this clusterfook.

Fast forward to 14:44 to hear his testimony.

Expert Panel Discussion on COVID-19 and Medical Freedom - Senator Mastriano

Time: Friday, March 4th from 9 – 11AM Location: Capitol (East Wing Room – 8E-A) Livestream: Senatormastriano.com/medicalfreedompanel Legislators Senator Doug Mastriano (Host) Senator Michelle Brooks (Chair of Senate Health and Human Services Committee) Representative Dawn Keefer Representative...

senatormastriano.com

 

[hemightbejeremy]

 

[UCFBS]

Again, this requires a basic understanding of middle school level math. During Covid, the death rate for the 85+ population went from 14.3% to 15.5% chance per year (an 8% increase). For the 35-44 population the death rate went from 0.25% to 0.38% chance per year (a 50+% increase). In reality the odds of an elderly dying increased by 1.2% during Covid and for a 35-44 year old increased by 1/10 of that amount. It’s basic to anyone who isn’t as dense as a black hole. Now this concludes your math lesson for the day.

If you read the chart ... it's 2021 August - December, when SARS-CoV-2 Delta deaths were going down, not up among 25-44. That's what Crazyhole is pointing out.

But let's just censor that chart and all data, because it destroys the narrative. Why are you guys for censorship?! Why?!

SARS-CoV-2 Delta killed a tiny fraction of 1% of those 25-44. So ... what could it be if not SARS-CoV-2 Delta?! Welcome to ****tardville ... population: you censors.

 

[Ucfmikes]

If you read the chart ... it's 2021 August - December, when SARS-CoV-2 Delta deaths were going down, not up among 25-44. That's what Crazyhole is pointing out.

But let's just censor that chart and all data, because it destroys the narrative. Why are you guys for censorship?! Why?!

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.

 

[Ucfmikes]

And here comes the parrot doing his typical cut and paste. Brainwashed.

View embedded media

Peter McCullough rips US safety and quality a new one. Everything he is saying is spot on. Made in America is DOA thanks to this clusterfook.

Fast forward to 14:44 to hear his testimony.

Expert Panel Discussion on COVID-19 and Medical Freedom - Senator Mastriano

Time: Friday, March 4th from 9 – 11AM Location: Capitol (East Wing Room – 8E-A) Livestream: Senatormastriano.com/medicalfreedompanel Legislators Senator Doug Mastriano (Host) Senator Michelle Brooks (Chair of Senate Health and Human Services Committee) Representative Dawn Keefer Representative...

senatormastriano.com

 

[Ucfmikes]

Safety of COVID-19 Vaccines
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.

 

[Ucfmikes]

 

[hemightbejeremy]

I’m not for censorship. Just eliminating all the fat people out there.

Hugs, chubby.

Who’s for censorship? I was just explaining why an increase from 2 to 3 is 50% and an increase from 10000 to 10800 is 8% but in absolute numbers the smaller percentage increase is actually a more significant increase. But you have to flip your brain switch to critical thinking mode rather than regurgitation of tweets based on a twitter search of antivaxxers. If crazyhole doesn’t like the answer to his question, it’s not censorship of his stupid chart.

 

[Crazyhole]

Who’s for censorship? I was just explaining why an increase from 2 to 3 is 50% and an increase from 10000 to 10800 is 8% but in absolute numbers the smaller percentage increase is actually a more significant increase. But you have to flip your brain switch to critical thinking mode rather than regurgitation of tweets based on a twitter search of antivaxxers. If crazyhole doesn’t like the answer to his question, it’s not censorship of his stupid chart.

I'm fine with your answer. The time frame just seems odd to me.

 

[Ucfmikes]

You aren’t dealing with someone who is particularly smart. But he is particularly celibate.

Wait? Wut? Mathematics and statistics aren’t taught in college? Oh wait…

 

[Ucfmikes]

I'm fine with your answer. The time frame just seems odd to me.

 

[NinjaKnight]

Who’s for censorship? I was just explaining why an increase from 2 to 3 is 50% and an increase from 10000 to 10800 is 8% but in absolute numbers the smaller percentage increase is actually a more significant increase. But you have to flip your brain switch to critical thinking mode rather than regurgitation of tweets based on a twitter search of antivaxxers. If crazyhole doesn’t like the answer to his question, it’s not censorship of his stupid chart.

Lmao imagine being a computer scientist and not understanding literal 3rd grade percentages 🤣😂🤣😂

How goddamn stupid are these people?

 

[Ucfmikes]

Lmao imagine being a computer scientist and not understanding literal 3rd grade percentages 🤣😂🤣😂

How goddamn stupid are these people?

Unemployed handyman with no high school diploma

 

[Ucfmikes]

The guidance from Florida states, healthy kids ages 5 to 17 may not benefit from the vaccine, and warns some 16 to 17-year-olds about the risk of myocarditis due to the COVID-19 vaccines may outweigh the benefits.

Continue...🍿

 

[Ucfmikes]

Safety of COVID-19 Vaccines
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.

 

[Ucfmikes]

Safety of COVID-19 Vaccines
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.

 

[Ucfmikes]

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[Ucfmikes]

Safety of COVID-19 Vaccines
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.

 

[Ucfmikes]

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.

 

[Ucfmikes]

Ha 🤣 🤣 🤣 🤣 ^^^^ 🤣🤣🤣🤣🤣

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.

 

[UCFBS]

Anyone still for vaccinating healthy 5 year olds?

🍿🍿🍿🍿

We've gotta vaccinate kids to protect the elderly! You're an idiot if you think otherwise! There's no risk! *

 

[Ucfmikes]

We've gotta vaccinate kids to protect the elderly! You're an idiot if you think otherwise! There's no risk! *

 

[Ucfmikes]

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.

 

[Ucfmikes]

🦜 vs 🦜 battle

I have my money on Mickey as the cut and paste King of the board.

@KNIGHTTIME^ today

 

[Ucfmikes]

🦜 vs 🦜 battle

I have my money on Mickey as the cut and paste King of the board.

^^^^^

 

[Crazyhole]

https://www.fda.gov/media/151733/download

Hmm. All cause mortality was 24% higher in the vaccinated group compared to the control group.

 

[Ucfmikes]

https://www.fda.gov/media/151733/download

Hmm. All cause mortality was 24% higher in the vaccinated group compared to the control group.

Safety of COVID-19 Vaccines
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.

 

[Ucfmikes]

https://www.fda.gov/media/151733/download

Hmm. All cause mortality was 24% higher in the vaccinated group compared to the control group.

 

[Ucfmikes]

https://www.fda.gov/media/151733/download

Hmm. All cause mortality was 24% higher in the vaccinated group compared to the control group.

 

[Crazyhole]

🐑

View embedded media

Wasn't Pfizer supposed to have an omicron vaccine by the first of March?